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NM_007294.4(BRCA1):c.3903T>A (p.Ser1301Arg) AND Breast-ovarian cancer, familial, susceptibility to, 1

Germline classification:
Uncertain significance (2 submissions)
Last evaluated:
Oct 19, 2011
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000077559.5

Allele description [Variation Report for NM_007294.4(BRCA1):c.3903T>A (p.Ser1301Arg)]

NM_007294.4(BRCA1):c.3903T>A (p.Ser1301Arg)

Genes:
BRCA1:BRCA1 DNA repair associated [Gene - OMIM - HGNC]
LOC126862571:BRD4-independent group 4 enhancer GRCh37_chr17:41243136-41244335 [Gene]
Variant type:
single nucleotide variant
Cytogenetic location:
17q21.31
Genomic location:
Preferred name:
NM_007294.4(BRCA1):c.3903T>A (p.Ser1301Arg)
HGVS:
  • NC_000017.11:g.43091628A>T
  • NG_005905.2:g.126356T>A
  • NG_087068.1:g.610A>T
  • NM_001407571.1:c.3690T>A
  • NM_001407581.1:c.3903T>A
  • NM_001407582.1:c.3903T>A
  • NM_001407583.1:c.3903T>A
  • NM_001407585.1:c.3903T>A
  • NM_001407587.1:c.3900T>A
  • NM_001407590.1:c.3900T>A
  • NM_001407591.1:c.3900T>A
  • NM_001407593.1:c.3903T>A
  • NM_001407594.1:c.3903T>A
  • NM_001407596.1:c.3903T>A
  • NM_001407597.1:c.3903T>A
  • NM_001407598.1:c.3903T>A
  • NM_001407602.1:c.3903T>A
  • NM_001407603.1:c.3903T>A
  • NM_001407605.1:c.3903T>A
  • NM_001407610.1:c.3900T>A
  • NM_001407611.1:c.3900T>A
  • NM_001407612.1:c.3900T>A
  • NM_001407613.1:c.3900T>A
  • NM_001407614.1:c.3900T>A
  • NM_001407615.1:c.3900T>A
  • NM_001407616.1:c.3903T>A
  • NM_001407617.1:c.3903T>A
  • NM_001407618.1:c.3903T>A
  • NM_001407619.1:c.3903T>A
  • NM_001407620.1:c.3903T>A
  • NM_001407621.1:c.3903T>A
  • NM_001407622.1:c.3903T>A
  • NM_001407623.1:c.3903T>A
  • NM_001407624.1:c.3903T>A
  • NM_001407625.1:c.3903T>A
  • NM_001407626.1:c.3903T>A
  • NM_001407627.1:c.3900T>A
  • NM_001407628.1:c.3900T>A
  • NM_001407629.1:c.3900T>A
  • NM_001407630.1:c.3900T>A
  • NM_001407631.1:c.3900T>A
  • NM_001407632.1:c.3900T>A
  • NM_001407633.1:c.3900T>A
  • NM_001407634.1:c.3900T>A
  • NM_001407635.1:c.3900T>A
  • NM_001407636.1:c.3900T>A
  • NM_001407637.1:c.3900T>A
  • NM_001407638.1:c.3900T>A
  • NM_001407639.1:c.3903T>A
  • NM_001407640.1:c.3903T>A
  • NM_001407641.1:c.3903T>A
  • NM_001407642.1:c.3903T>A
  • NM_001407644.1:c.3900T>A
  • NM_001407645.1:c.3900T>A
  • NM_001407646.1:c.3894T>A
  • NM_001407647.1:c.3894T>A
  • NM_001407648.1:c.3780T>A
  • NM_001407649.1:c.3777T>A
  • NM_001407652.1:c.3903T>A
  • NM_001407653.1:c.3825T>A
  • NM_001407654.1:c.3825T>A
  • NM_001407655.1:c.3825T>A
  • NM_001407656.1:c.3825T>A
  • NM_001407657.1:c.3825T>A
  • NM_001407658.1:c.3825T>A
  • NM_001407659.1:c.3822T>A
  • NM_001407660.1:c.3822T>A
  • NM_001407661.1:c.3822T>A
  • NM_001407662.1:c.3822T>A
  • NM_001407663.1:c.3825T>A
  • NM_001407664.1:c.3780T>A
  • NM_001407665.1:c.3780T>A
  • NM_001407666.1:c.3780T>A
  • NM_001407667.1:c.3780T>A
  • NM_001407668.1:c.3780T>A
  • NM_001407669.1:c.3780T>A
  • NM_001407670.1:c.3777T>A
  • NM_001407671.1:c.3777T>A
  • NM_001407672.1:c.3777T>A
  • NM_001407673.1:c.3777T>A
  • NM_001407674.1:c.3780T>A
  • NM_001407675.1:c.3780T>A
  • NM_001407676.1:c.3780T>A
  • NM_001407677.1:c.3780T>A
  • NM_001407678.1:c.3780T>A
  • NM_001407679.1:c.3780T>A
  • NM_001407680.1:c.3780T>A
  • NM_001407681.1:c.3780T>A
  • NM_001407682.1:c.3780T>A
  • NM_001407683.1:c.3780T>A
  • NM_001407684.1:c.3903T>A
  • NM_001407685.1:c.3777T>A
  • NM_001407686.1:c.3777T>A
  • NM_001407687.1:c.3777T>A
  • NM_001407688.1:c.3777T>A
  • NM_001407689.1:c.3777T>A
  • NM_001407690.1:c.3777T>A
  • NM_001407691.1:c.3777T>A
  • NM_001407692.1:c.3762T>A
  • NM_001407694.1:c.3762T>A
  • NM_001407695.1:c.3762T>A
  • NM_001407696.1:c.3762T>A
  • NM_001407697.1:c.3762T>A
  • NM_001407698.1:c.3762T>A
  • NM_001407724.1:c.3762T>A
  • NM_001407725.1:c.3762T>A
  • NM_001407726.1:c.3762T>A
  • NM_001407727.1:c.3762T>A
  • NM_001407728.1:c.3762T>A
  • NM_001407729.1:c.3762T>A
  • NM_001407730.1:c.3762T>A
  • NM_001407731.1:c.3762T>A
  • NM_001407732.1:c.3762T>A
  • NM_001407733.1:c.3762T>A
  • NM_001407734.1:c.3762T>A
  • NM_001407735.1:c.3762T>A
  • NM_001407736.1:c.3762T>A
  • NM_001407737.1:c.3762T>A
  • NM_001407738.1:c.3762T>A
  • NM_001407739.1:c.3762T>A
  • NM_001407740.1:c.3759T>A
  • NM_001407741.1:c.3759T>A
  • NM_001407742.1:c.3759T>A
  • NM_001407743.1:c.3759T>A
  • NM_001407744.1:c.3759T>A
  • NM_001407745.1:c.3759T>A
  • NM_001407746.1:c.3759T>A
  • NM_001407747.1:c.3759T>A
  • NM_001407748.1:c.3759T>A
  • NM_001407749.1:c.3759T>A
  • NM_001407750.1:c.3762T>A
  • NM_001407751.1:c.3762T>A
  • NM_001407752.1:c.3762T>A
  • NM_001407838.1:c.3759T>A
  • NM_001407839.1:c.3759T>A
  • NM_001407841.1:c.3759T>A
  • NM_001407842.1:c.3759T>A
  • NM_001407843.1:c.3759T>A
  • NM_001407844.1:c.3759T>A
  • NM_001407845.1:c.3759T>A
  • NM_001407846.1:c.3759T>A
  • NM_001407847.1:c.3759T>A
  • NM_001407848.1:c.3759T>A
  • NM_001407849.1:c.3759T>A
  • NM_001407850.1:c.3762T>A
  • NM_001407851.1:c.3762T>A
  • NM_001407852.1:c.3762T>A
  • NM_001407853.1:c.3690T>A
  • NM_001407854.1:c.3903T>A
  • NM_001407858.1:c.3903T>A
  • NM_001407859.1:c.3903T>A
  • NM_001407860.1:c.3900T>A
  • NM_001407861.1:c.3900T>A
  • NM_001407862.1:c.3702T>A
  • NM_001407863.1:c.3780T>A
  • NM_001407874.1:c.3699T>A
  • NM_001407875.1:c.3699T>A
  • NM_001407879.1:c.3693T>A
  • NM_001407881.1:c.3693T>A
  • NM_001407882.1:c.3693T>A
  • NM_001407884.1:c.3693T>A
  • NM_001407885.1:c.3693T>A
  • NM_001407886.1:c.3693T>A
  • NM_001407887.1:c.3693T>A
  • NM_001407889.1:c.3693T>A
  • NM_001407894.1:c.3690T>A
  • NM_001407895.1:c.3690T>A
  • NM_001407896.1:c.3690T>A
  • NM_001407897.1:c.3690T>A
  • NM_001407898.1:c.3690T>A
  • NM_001407899.1:c.3690T>A
  • NM_001407900.1:c.3693T>A
  • NM_001407902.1:c.3693T>A
  • NM_001407904.1:c.3693T>A
  • NM_001407906.1:c.3693T>A
  • NM_001407907.1:c.3693T>A
  • NM_001407908.1:c.3693T>A
  • NM_001407909.1:c.3693T>A
  • NM_001407910.1:c.3693T>A
  • NM_001407915.1:c.3690T>A
  • NM_001407916.1:c.3690T>A
  • NM_001407917.1:c.3690T>A
  • NM_001407918.1:c.3690T>A
  • NM_001407919.1:c.3780T>A
  • NM_001407920.1:c.3639T>A
  • NM_001407921.1:c.3639T>A
  • NM_001407922.1:c.3639T>A
  • NM_001407923.1:c.3639T>A
  • NM_001407924.1:c.3639T>A
  • NM_001407925.1:c.3639T>A
  • NM_001407926.1:c.3639T>A
  • NM_001407927.1:c.3639T>A
  • NM_001407928.1:c.3639T>A
  • NM_001407929.1:c.3639T>A
  • NM_001407930.1:c.3636T>A
  • NM_001407931.1:c.3636T>A
  • NM_001407932.1:c.3636T>A
  • NM_001407933.1:c.3639T>A
  • NM_001407934.1:c.3636T>A
  • NM_001407935.1:c.3639T>A
  • NM_001407936.1:c.3636T>A
  • NM_001407937.1:c.3780T>A
  • NM_001407938.1:c.3780T>A
  • NM_001407939.1:c.3780T>A
  • NM_001407940.1:c.3777T>A
  • NM_001407941.1:c.3777T>A
  • NM_001407942.1:c.3762T>A
  • NM_001407943.1:c.3759T>A
  • NM_001407944.1:c.3762T>A
  • NM_001407945.1:c.3762T>A
  • NM_001407946.1:c.3570T>A
  • NM_001407947.1:c.3570T>A
  • NM_001407948.1:c.3570T>A
  • NM_001407949.1:c.3570T>A
  • NM_001407950.1:c.3570T>A
  • NM_001407951.1:c.3570T>A
  • NM_001407952.1:c.3570T>A
  • NM_001407953.1:c.3570T>A
  • NM_001407954.1:c.3567T>A
  • NM_001407955.1:c.3567T>A
  • NM_001407956.1:c.3567T>A
  • NM_001407957.1:c.3570T>A
  • NM_001407958.1:c.3567T>A
  • NM_001407959.1:c.3522T>A
  • NM_001407960.1:c.3522T>A
  • NM_001407962.1:c.3519T>A
  • NM_001407963.1:c.3522T>A
  • NM_001407964.1:c.3759T>A
  • NM_001407965.1:c.3399T>A
  • NM_001407966.1:c.3015T>A
  • NM_001407967.1:c.3015T>A
  • NM_001407968.1:c.1299T>A
  • NM_001407969.1:c.1299T>A
  • NM_001407970.1:c.788-596T>A
  • NM_001407971.1:c.788-596T>A
  • NM_001407972.1:c.785-596T>A
  • NM_001407973.1:c.788-596T>A
  • NM_001407974.1:c.788-596T>A
  • NM_001407975.1:c.788-596T>A
  • NM_001407976.1:c.788-596T>A
  • NM_001407977.1:c.788-596T>A
  • NM_001407978.1:c.788-596T>A
  • NM_001407979.1:c.788-596T>A
  • NM_001407980.1:c.788-596T>A
  • NM_001407981.1:c.788-596T>A
  • NM_001407982.1:c.788-596T>A
  • NM_001407983.1:c.788-596T>A
  • NM_001407984.1:c.785-596T>A
  • NM_001407985.1:c.785-596T>A
  • NM_001407986.1:c.785-596T>A
  • NM_001407990.1:c.788-596T>A
  • NM_001407991.1:c.785-596T>A
  • NM_001407992.1:c.785-596T>A
  • NM_001407993.1:c.788-596T>A
  • NM_001408392.1:c.785-596T>A
  • NM_001408396.1:c.785-596T>A
  • NM_001408397.1:c.785-596T>A
  • NM_001408398.1:c.785-596T>A
  • NM_001408399.1:c.785-596T>A
  • NM_001408400.1:c.785-596T>A
  • NM_001408401.1:c.785-596T>A
  • NM_001408402.1:c.785-596T>A
  • NM_001408403.1:c.788-596T>A
  • NM_001408404.1:c.788-596T>A
  • NM_001408406.1:c.791-605T>A
  • NM_001408407.1:c.785-596T>A
  • NM_001408408.1:c.779-596T>A
  • NM_001408409.1:c.710-596T>A
  • NM_001408410.1:c.647-596T>A
  • NM_001408411.1:c.710-596T>A
  • NM_001408412.1:c.710-596T>A
  • NM_001408413.1:c.707-596T>A
  • NM_001408414.1:c.710-596T>A
  • NM_001408415.1:c.710-596T>A
  • NM_001408416.1:c.707-596T>A
  • NM_001408418.1:c.671-596T>A
  • NM_001408419.1:c.671-596T>A
  • NM_001408420.1:c.671-596T>A
  • NM_001408421.1:c.668-596T>A
  • NM_001408422.1:c.671-596T>A
  • NM_001408423.1:c.671-596T>A
  • NM_001408424.1:c.668-596T>A
  • NM_001408425.1:c.665-596T>A
  • NM_001408426.1:c.665-596T>A
  • NM_001408427.1:c.665-596T>A
  • NM_001408428.1:c.665-596T>A
  • NM_001408429.1:c.665-596T>A
  • NM_001408430.1:c.665-596T>A
  • NM_001408431.1:c.668-596T>A
  • NM_001408432.1:c.662-596T>A
  • NM_001408433.1:c.662-596T>A
  • NM_001408434.1:c.662-596T>A
  • NM_001408435.1:c.662-596T>A
  • NM_001408436.1:c.665-596T>A
  • NM_001408437.1:c.665-596T>A
  • NM_001408438.1:c.665-596T>A
  • NM_001408439.1:c.665-596T>A
  • NM_001408440.1:c.665-596T>A
  • NM_001408441.1:c.665-596T>A
  • NM_001408442.1:c.665-596T>A
  • NM_001408443.1:c.665-596T>A
  • NM_001408444.1:c.665-596T>A
  • NM_001408445.1:c.662-596T>A
  • NM_001408446.1:c.662-596T>A
  • NM_001408447.1:c.662-596T>A
  • NM_001408448.1:c.662-596T>A
  • NM_001408450.1:c.662-596T>A
  • NM_001408451.1:c.653-596T>A
  • NM_001408452.1:c.647-596T>A
  • NM_001408453.1:c.647-596T>A
  • NM_001408454.1:c.647-596T>A
  • NM_001408455.1:c.647-596T>A
  • NM_001408456.1:c.647-596T>A
  • NM_001408457.1:c.647-596T>A
  • NM_001408458.1:c.647-596T>A
  • NM_001408459.1:c.647-596T>A
  • NM_001408460.1:c.647-596T>A
  • NM_001408461.1:c.647-596T>A
  • NM_001408462.1:c.644-596T>A
  • NM_001408463.1:c.644-596T>A
  • NM_001408464.1:c.644-596T>A
  • NM_001408465.1:c.644-596T>A
  • NM_001408466.1:c.647-596T>A
  • NM_001408467.1:c.647-596T>A
  • NM_001408468.1:c.644-596T>A
  • NM_001408469.1:c.647-596T>A
  • NM_001408470.1:c.644-596T>A
  • NM_001408472.1:c.788-596T>A
  • NM_001408473.1:c.785-596T>A
  • NM_001408474.1:c.587-596T>A
  • NM_001408475.1:c.584-596T>A
  • NM_001408476.1:c.587-596T>A
  • NM_001408478.1:c.578-596T>A
  • NM_001408479.1:c.578-596T>A
  • NM_001408480.1:c.578-596T>A
  • NM_001408481.1:c.578-596T>A
  • NM_001408482.1:c.578-596T>A
  • NM_001408483.1:c.578-596T>A
  • NM_001408484.1:c.578-596T>A
  • NM_001408485.1:c.578-596T>A
  • NM_001408489.1:c.578-596T>A
  • NM_001408490.1:c.575-596T>A
  • NM_001408491.1:c.575-596T>A
  • NM_001408492.1:c.578-596T>A
  • NM_001408493.1:c.575-596T>A
  • NM_001408494.1:c.548-596T>A
  • NM_001408495.1:c.545-596T>A
  • NM_001408496.1:c.524-596T>A
  • NM_001408497.1:c.524-596T>A
  • NM_001408498.1:c.524-596T>A
  • NM_001408499.1:c.524-596T>A
  • NM_001408500.1:c.524-596T>A
  • NM_001408501.1:c.524-596T>A
  • NM_001408502.1:c.455-596T>A
  • NM_001408503.1:c.521-596T>A
  • NM_001408504.1:c.521-596T>A
  • NM_001408505.1:c.521-596T>A
  • NM_001408506.1:c.461-596T>A
  • NM_001408507.1:c.461-596T>A
  • NM_001408508.1:c.452-596T>A
  • NM_001408509.1:c.452-596T>A
  • NM_001408510.1:c.407-596T>A
  • NM_001408511.1:c.404-596T>A
  • NM_001408512.1:c.284-596T>A
  • NM_001408513.1:c.578-596T>A
  • NM_001408514.1:c.578-596T>A
  • NM_007294.4:c.3903T>AMANE SELECT
  • NM_007297.4:c.3762T>A
  • NM_007298.4:c.788-596T>A
  • NM_007299.4:c.788-596T>A
  • NM_007300.4:c.3903T>A
  • NP_001394500.1:p.Ser1230Arg
  • NP_001394510.1:p.Ser1301Arg
  • NP_001394511.1:p.Ser1301Arg
  • NP_001394512.1:p.Ser1301Arg
  • NP_001394514.1:p.Ser1301Arg
  • NP_001394516.1:p.Ser1300Arg
  • NP_001394519.1:p.Ser1300Arg
  • NP_001394520.1:p.Ser1300Arg
  • NP_001394522.1:p.Ser1301Arg
  • NP_001394523.1:p.Ser1301Arg
  • NP_001394525.1:p.Ser1301Arg
  • NP_001394526.1:p.Ser1301Arg
  • NP_001394527.1:p.Ser1301Arg
  • NP_001394531.1:p.Ser1301Arg
  • NP_001394532.1:p.Ser1301Arg
  • NP_001394534.1:p.Ser1301Arg
  • NP_001394539.1:p.Ser1300Arg
  • NP_001394540.1:p.Ser1300Arg
  • NP_001394541.1:p.Ser1300Arg
  • NP_001394542.1:p.Ser1300Arg
  • NP_001394543.1:p.Ser1300Arg
  • NP_001394544.1:p.Ser1300Arg
  • NP_001394545.1:p.Ser1301Arg
  • NP_001394546.1:p.Ser1301Arg
  • NP_001394547.1:p.Ser1301Arg
  • NP_001394548.1:p.Ser1301Arg
  • NP_001394549.1:p.Ser1301Arg
  • NP_001394550.1:p.Ser1301Arg
  • NP_001394551.1:p.Ser1301Arg
  • NP_001394552.1:p.Ser1301Arg
  • NP_001394553.1:p.Ser1301Arg
  • NP_001394554.1:p.Ser1301Arg
  • NP_001394555.1:p.Ser1301Arg
  • NP_001394556.1:p.Ser1300Arg
  • NP_001394557.1:p.Ser1300Arg
  • NP_001394558.1:p.Ser1300Arg
  • NP_001394559.1:p.Ser1300Arg
  • NP_001394560.1:p.Ser1300Arg
  • NP_001394561.1:p.Ser1300Arg
  • NP_001394562.1:p.Ser1300Arg
  • NP_001394563.1:p.Ser1300Arg
  • NP_001394564.1:p.Ser1300Arg
  • NP_001394565.1:p.Ser1300Arg
  • NP_001394566.1:p.Ser1300Arg
  • NP_001394567.1:p.Ser1300Arg
  • NP_001394568.1:p.Ser1301Arg
  • NP_001394569.1:p.Ser1301Arg
  • NP_001394570.1:p.Ser1301Arg
  • NP_001394571.1:p.Ser1301Arg
  • NP_001394573.1:p.Ser1300Arg
  • NP_001394574.1:p.Ser1300Arg
  • NP_001394575.1:p.Ser1298Arg
  • NP_001394576.1:p.Ser1298Arg
  • NP_001394577.1:p.Ser1260Arg
  • NP_001394578.1:p.Ser1259Arg
  • NP_001394581.1:p.Ser1301Arg
  • NP_001394582.1:p.Ser1275Arg
  • NP_001394583.1:p.Ser1275Arg
  • NP_001394584.1:p.Ser1275Arg
  • NP_001394585.1:p.Ser1275Arg
  • NP_001394586.1:p.Ser1275Arg
  • NP_001394587.1:p.Ser1275Arg
  • NP_001394588.1:p.Ser1274Arg
  • NP_001394589.1:p.Ser1274Arg
  • NP_001394590.1:p.Ser1274Arg
  • NP_001394591.1:p.Ser1274Arg
  • NP_001394592.1:p.Ser1275Arg
  • NP_001394593.1:p.Ser1260Arg
  • NP_001394594.1:p.Ser1260Arg
  • NP_001394595.1:p.Ser1260Arg
  • NP_001394596.1:p.Ser1260Arg
  • NP_001394597.1:p.Ser1260Arg
  • NP_001394598.1:p.Ser1260Arg
  • NP_001394599.1:p.Ser1259Arg
  • NP_001394600.1:p.Ser1259Arg
  • NP_001394601.1:p.Ser1259Arg
  • NP_001394602.1:p.Ser1259Arg
  • NP_001394603.1:p.Ser1260Arg
  • NP_001394604.1:p.Ser1260Arg
  • NP_001394605.1:p.Ser1260Arg
  • NP_001394606.1:p.Ser1260Arg
  • NP_001394607.1:p.Ser1260Arg
  • NP_001394608.1:p.Ser1260Arg
  • NP_001394609.1:p.Ser1260Arg
  • NP_001394610.1:p.Ser1260Arg
  • NP_001394611.1:p.Ser1260Arg
  • NP_001394612.1:p.Ser1260Arg
  • NP_001394613.1:p.Ser1301Arg
  • NP_001394614.1:p.Ser1259Arg
  • NP_001394615.1:p.Ser1259Arg
  • NP_001394616.1:p.Ser1259Arg
  • NP_001394617.1:p.Ser1259Arg
  • NP_001394618.1:p.Ser1259Arg
  • NP_001394619.1:p.Ser1259Arg
  • NP_001394620.1:p.Ser1259Arg
  • NP_001394621.1:p.Ser1254Arg
  • NP_001394623.1:p.Ser1254Arg
  • NP_001394624.1:p.Ser1254Arg
  • NP_001394625.1:p.Ser1254Arg
  • NP_001394626.1:p.Ser1254Arg
  • NP_001394627.1:p.Ser1254Arg
  • NP_001394653.1:p.Ser1254Arg
  • NP_001394654.1:p.Ser1254Arg
  • NP_001394655.1:p.Ser1254Arg
  • NP_001394656.1:p.Ser1254Arg
  • NP_001394657.1:p.Ser1254Arg
  • NP_001394658.1:p.Ser1254Arg
  • NP_001394659.1:p.Ser1254Arg
  • NP_001394660.1:p.Ser1254Arg
  • NP_001394661.1:p.Ser1254Arg
  • NP_001394662.1:p.Ser1254Arg
  • NP_001394663.1:p.Ser1254Arg
  • NP_001394664.1:p.Ser1254Arg
  • NP_001394665.1:p.Ser1254Arg
  • NP_001394666.1:p.Ser1254Arg
  • NP_001394667.1:p.Ser1254Arg
  • NP_001394668.1:p.Ser1254Arg
  • NP_001394669.1:p.Ser1253Arg
  • NP_001394670.1:p.Ser1253Arg
  • NP_001394671.1:p.Ser1253Arg
  • NP_001394672.1:p.Ser1253Arg
  • NP_001394673.1:p.Ser1253Arg
  • NP_001394674.1:p.Ser1253Arg
  • NP_001394675.1:p.Ser1253Arg
  • NP_001394676.1:p.Ser1253Arg
  • NP_001394677.1:p.Ser1253Arg
  • NP_001394678.1:p.Ser1253Arg
  • NP_001394679.1:p.Ser1254Arg
  • NP_001394680.1:p.Ser1254Arg
  • NP_001394681.1:p.Ser1254Arg
  • NP_001394767.1:p.Ser1253Arg
  • NP_001394768.1:p.Ser1253Arg
  • NP_001394770.1:p.Ser1253Arg
  • NP_001394771.1:p.Ser1253Arg
  • NP_001394772.1:p.Ser1253Arg
  • NP_001394773.1:p.Ser1253Arg
  • NP_001394774.1:p.Ser1253Arg
  • NP_001394775.1:p.Ser1253Arg
  • NP_001394776.1:p.Ser1253Arg
  • NP_001394777.1:p.Ser1253Arg
  • NP_001394778.1:p.Ser1253Arg
  • NP_001394779.1:p.Ser1254Arg
  • NP_001394780.1:p.Ser1254Arg
  • NP_001394781.1:p.Ser1254Arg
  • NP_001394782.1:p.Ser1230Arg
  • NP_001394783.1:p.Ser1301Arg
  • NP_001394787.1:p.Ser1301Arg
  • NP_001394788.1:p.Ser1301Arg
  • NP_001394789.1:p.Ser1300Arg
  • NP_001394790.1:p.Ser1300Arg
  • NP_001394791.1:p.Ser1234Arg
  • NP_001394792.1:p.Ser1260Arg
  • NP_001394803.1:p.Ser1233Arg
  • NP_001394804.1:p.Ser1233Arg
  • NP_001394808.1:p.Ser1231Arg
  • NP_001394810.1:p.Ser1231Arg
  • NP_001394811.1:p.Ser1231Arg
  • NP_001394813.1:p.Ser1231Arg
  • NP_001394814.1:p.Ser1231Arg
  • NP_001394815.1:p.Ser1231Arg
  • NP_001394816.1:p.Ser1231Arg
  • NP_001394818.1:p.Ser1231Arg
  • NP_001394823.1:p.Ser1230Arg
  • NP_001394824.1:p.Ser1230Arg
  • NP_001394825.1:p.Ser1230Arg
  • NP_001394826.1:p.Ser1230Arg
  • NP_001394827.1:p.Ser1230Arg
  • NP_001394828.1:p.Ser1230Arg
  • NP_001394829.1:p.Ser1231Arg
  • NP_001394831.1:p.Ser1231Arg
  • NP_001394833.1:p.Ser1231Arg
  • NP_001394835.1:p.Ser1231Arg
  • NP_001394836.1:p.Ser1231Arg
  • NP_001394837.1:p.Ser1231Arg
  • NP_001394838.1:p.Ser1231Arg
  • NP_001394839.1:p.Ser1231Arg
  • NP_001394844.1:p.Ser1230Arg
  • NP_001394845.1:p.Ser1230Arg
  • NP_001394846.1:p.Ser1230Arg
  • NP_001394847.1:p.Ser1230Arg
  • NP_001394848.1:p.Ser1260Arg
  • NP_001394849.1:p.Ser1213Arg
  • NP_001394850.1:p.Ser1213Arg
  • NP_001394851.1:p.Ser1213Arg
  • NP_001394852.1:p.Ser1213Arg
  • NP_001394853.1:p.Ser1213Arg
  • NP_001394854.1:p.Ser1213Arg
  • NP_001394855.1:p.Ser1213Arg
  • NP_001394856.1:p.Ser1213Arg
  • NP_001394857.1:p.Ser1213Arg
  • NP_001394858.1:p.Ser1213Arg
  • NP_001394859.1:p.Ser1212Arg
  • NP_001394860.1:p.Ser1212Arg
  • NP_001394861.1:p.Ser1212Arg
  • NP_001394862.1:p.Ser1213Arg
  • NP_001394863.1:p.Ser1212Arg
  • NP_001394864.1:p.Ser1213Arg
  • NP_001394865.1:p.Ser1212Arg
  • NP_001394866.1:p.Ser1260Arg
  • NP_001394867.1:p.Ser1260Arg
  • NP_001394868.1:p.Ser1260Arg
  • NP_001394869.1:p.Ser1259Arg
  • NP_001394870.1:p.Ser1259Arg
  • NP_001394871.1:p.Ser1254Arg
  • NP_001394872.1:p.Ser1253Arg
  • NP_001394873.1:p.Ser1254Arg
  • NP_001394874.1:p.Ser1254Arg
  • NP_001394875.1:p.Ser1190Arg
  • NP_001394876.1:p.Ser1190Arg
  • NP_001394877.1:p.Ser1190Arg
  • NP_001394878.1:p.Ser1190Arg
  • NP_001394879.1:p.Ser1190Arg
  • NP_001394880.1:p.Ser1190Arg
  • NP_001394881.1:p.Ser1190Arg
  • NP_001394882.1:p.Ser1190Arg
  • NP_001394883.1:p.Ser1189Arg
  • NP_001394884.1:p.Ser1189Arg
  • NP_001394885.1:p.Ser1189Arg
  • NP_001394886.1:p.Ser1190Arg
  • NP_001394887.1:p.Ser1189Arg
  • NP_001394888.1:p.Ser1174Arg
  • NP_001394889.1:p.Ser1174Arg
  • NP_001394891.1:p.Ser1173Arg
  • NP_001394892.1:p.Ser1174Arg
  • NP_001394893.1:p.Ser1253Arg
  • NP_001394894.1:p.Ser1133Arg
  • NP_001394895.1:p.Ser1005Arg
  • NP_001394896.1:p.Ser1005Arg
  • NP_001394897.1:p.Ser433Arg
  • NP_001394898.1:p.Ser433Arg
  • NP_009225.1:p.Ser1301Arg
  • NP_009225.1:p.Ser1301Arg
  • NP_009228.2:p.Ser1254Arg
  • NP_009231.2:p.Ser1301Arg
  • LRG_292t1:c.3903T>A
  • LRG_292:g.126356T>A
  • LRG_292p1:p.Ser1301Arg
  • NC_000017.10:g.41243645A>T
  • NM_007294.3:c.3903T>A
  • NR_027676.1:n.4039T>A
  • P38398:p.Ser1301Arg
  • U14680.1:n.4022T>A
Nucleotide change:
4022T>A
Protein change:
S1005R
Links:
UniProtKB: P38398#VAR_070485; dbSNP: rs273900719
NCBI 1000 Genomes Browser:
rs273900719
Molecular consequence:
  • NM_001407970.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407971.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407972.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407973.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407974.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407975.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407976.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407977.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407978.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407979.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407980.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407981.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407982.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407983.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407984.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407985.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407986.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407990.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407991.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407992.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407993.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408392.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408396.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408397.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408398.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408399.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408400.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408401.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408402.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408403.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408404.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408406.1:c.791-605T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408407.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408408.1:c.779-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408409.1:c.710-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408410.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408411.1:c.710-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408412.1:c.710-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408413.1:c.707-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408414.1:c.710-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408415.1:c.710-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408416.1:c.707-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408418.1:c.671-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408419.1:c.671-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408420.1:c.671-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408421.1:c.668-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408422.1:c.671-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408423.1:c.671-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408424.1:c.668-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408425.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408426.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408427.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408428.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408429.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408430.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408431.1:c.668-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408432.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408433.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408434.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408435.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408436.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408437.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408438.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408439.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408440.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408441.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408442.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408443.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408444.1:c.665-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408445.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408446.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408447.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408448.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408450.1:c.662-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408451.1:c.653-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408452.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408453.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408454.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408455.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408456.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408457.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408458.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408459.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408460.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408461.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408462.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408463.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408464.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408465.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408466.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408467.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408468.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408469.1:c.647-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408470.1:c.644-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408472.1:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408473.1:c.785-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408474.1:c.587-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408475.1:c.584-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408476.1:c.587-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408478.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408479.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408480.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408481.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408482.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408483.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408484.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408485.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408489.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408490.1:c.575-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408491.1:c.575-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408492.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408493.1:c.575-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408494.1:c.548-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408495.1:c.545-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408496.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408497.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408498.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408499.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408500.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408501.1:c.524-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408502.1:c.455-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408503.1:c.521-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408504.1:c.521-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408505.1:c.521-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408506.1:c.461-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408507.1:c.461-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408508.1:c.452-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408509.1:c.452-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408510.1:c.407-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408511.1:c.404-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408512.1:c.284-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408513.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001408514.1:c.578-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007298.4:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_007299.4:c.788-596T>A - intron variant - [Sequence Ontology: SO:0001627]
  • NM_001407571.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407581.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407582.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407583.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407585.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407587.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407590.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407591.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407593.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407594.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407596.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407597.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407598.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407602.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407603.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407605.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407610.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407611.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407612.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407613.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407614.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407615.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407616.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407617.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407618.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407619.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407620.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407621.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407622.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407623.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407624.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407625.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407626.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407627.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407628.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407629.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407630.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407631.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407632.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407633.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407634.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407635.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407636.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407637.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407638.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407639.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407640.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407641.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407642.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407644.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407645.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407646.1:c.3894T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407647.1:c.3894T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407648.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407649.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407652.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407653.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407654.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407655.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407656.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407657.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407658.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407659.1:c.3822T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407660.1:c.3822T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407661.1:c.3822T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407662.1:c.3822T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407663.1:c.3825T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407664.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407665.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407666.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407667.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407668.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407669.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407670.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407671.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407672.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407673.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407674.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407675.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407676.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407677.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407678.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407679.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407680.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407681.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407682.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407683.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407684.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407685.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407686.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407687.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407688.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407689.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407690.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407691.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407692.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407694.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407695.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407696.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407697.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407698.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407724.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407725.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407726.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407727.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407728.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407729.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407730.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407731.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407732.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407733.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407734.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407735.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407736.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407737.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407738.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407739.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407740.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407741.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407742.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407743.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407744.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407745.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407746.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407747.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407748.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407749.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407750.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407751.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407752.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407838.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407839.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407841.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407842.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407843.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407844.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407845.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407846.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407847.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407848.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407849.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407850.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407851.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407852.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407853.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407854.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407858.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407859.1:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407860.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407861.1:c.3900T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407862.1:c.3702T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407863.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407874.1:c.3699T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407875.1:c.3699T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407879.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407881.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407882.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407884.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407885.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407886.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407887.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407889.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407894.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407895.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407896.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407897.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407898.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407899.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407900.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407902.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407904.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407906.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407907.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407908.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407909.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407910.1:c.3693T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407915.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407916.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407917.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407918.1:c.3690T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407919.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407920.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407921.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407922.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407923.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407924.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407925.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407926.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407927.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407928.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407929.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407930.1:c.3636T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407931.1:c.3636T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407932.1:c.3636T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407933.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407934.1:c.3636T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407935.1:c.3639T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407936.1:c.3636T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407937.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407938.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407939.1:c.3780T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407940.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407941.1:c.3777T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407942.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407943.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407944.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407945.1:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407946.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407947.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407948.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407949.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407950.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407951.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407952.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407953.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407954.1:c.3567T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407955.1:c.3567T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407956.1:c.3567T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407957.1:c.3570T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407958.1:c.3567T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407959.1:c.3522T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407960.1:c.3522T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407962.1:c.3519T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407963.1:c.3522T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407964.1:c.3759T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407965.1:c.3399T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407966.1:c.3015T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407967.1:c.3015T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407968.1:c.1299T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_001407969.1:c.1299T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007294.4:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007297.4:c.3762T>A - missense variant - [Sequence Ontology: SO:0001583]
  • NM_007300.4:c.3903T>A - missense variant - [Sequence Ontology: SO:0001583]
Observations:
2

Condition(s)

Name:
Breast-ovarian cancer, familial, susceptibility to, 1 (BROVCA1)
Synonyms:
OVARIAN CANCER, SUSCEPTIBILITY TO; Breast cancer, familial 1
Identifiers:
MONDO: MONDO:0011450; MedGen: C2676676; Orphanet: 145; OMIM: 604370

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000109361Sharing Clinical Reports Project (SCRP)
no assertion criteria provided
Uncertain significance
(Apr 21, 2011)
germlineclinical testing

SCV000144913Breast Cancer Information Core (BIC) (BRCA1)
no assertion criteria provided
Uncertain significance
(Oct 19, 2011)
somaticclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedgermlinenot provided1not providednot provided1not providedclinical testing
Caucasiansomaticyes1not providednot providednot providednot providedclinical testing

Details of each submission

From Sharing Clinical Reports Project (SCRP), SCV000109361.2

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1germlinenot provided1not providednot providednot providednot providednot providednot provided

From Breast Cancer Information Core (BIC) (BRCA1), SCV000144913.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1Caucasian1not providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1somaticyesnot providednot providednot provided1not providednot providednot provided

Last Updated: Oct 8, 2024