"PreventionGenetics, part of Exact Sciences"[submitter] AND "NCOR1"[ge - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726341	NM_006311.4(NCOR1):c.7074A>G (p.Ser2358=)	NCOR1, TTC19	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign/Likely benign
Select item 722211	NM_006311.4(NCOR1):c.6870G>A (p.Met2290Ile)	NCOR1, TTC19 (M2290I +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 2633641	NM_006311.4(NCOR1):c.6728C>T (p.Thr2243Met)	NCOR1, TTC19 (T2140M +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 3058498	NM_006311.4(NCOR1):c.6678G>A (p.Met2226Ile)	NCOR1 (M2123I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 771023	NM_006311.4(NCOR1):c.6544G>A (p.Ala2182Thr)	NCOR1 (A2079T +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder +1 more	GBenign
Select item 722887	NM_006311.4(NCOR1):c.6468G>A (p.Pro2156=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign/Likely benign
Select item 3050696	NM_006311.4(NCOR1):c.6441C>T (p.Tyr2147=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 784667	NM_006311.4(NCOR1):c.6396G>A (p.Arg2132=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign
Select item 3049019	NM_006311.4(NCOR1):c.6312A>G (p.Glu2104=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 710458	NM_006311.4(NCOR1):c.6165C>A (p.Ile2055=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3054351	NM_006311.4(NCOR1):c.6010+6T>C	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GLikely benign
Select item 3056111	NM_006311.4(NCOR1):c.5986GTT[1] (p.Val1997del)	NCOR1 (V1894del +1 more)	Microsatellite (inframe deletion)	NCOR1-related disorder	GBenign
Select item 712852	NM_006311.4(NCOR1):c.5970G>A (p.Gln1990=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign
Select item 2632202	NM_006311.4(NCOR1):c.5831A>T (p.Asp1944Val)	NCOR1 (D1944V)	Single nucleotide variant (missense variant +1 more)	NCOR1-related disorder	GUncertain significance
Select item 3038963	NM_006311.4(NCOR1):c.5076G>A (p.Pro1692=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 777134	NM_006311.4(NCOR1):c.4863A>G (p.Gln1621=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign
Select item 3031103	NM_006311.4(NCOR1):c.4505C>T (p.Thr1502Ile)	NCOR1 (T1502I +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GUncertain significance
Select item 747294	NM_006311.4(NCOR1):c.4329C>T (p.Thr1443=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign/Likely benign
Select item 777715	NM_006311.4(NCOR1):c.4218A>C (p.Leu1406Phe)	NCOR1 (L1406F +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3059996	NM_006311.4(NCOR1):c.4153-5T>A	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GBenign
Select item 768834	NM_006311.4(NCOR1):c.4044G>A (p.Gly1348=)	NCOR1	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 3035259	NM_006311.4(NCOR1):c.3686G>A (p.Arg1229Gln)	NCOR1 (R1229Q +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3056547	NM_006311.4(NCOR1):c.3436C>A (p.Arg1146=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3035132	NM_006311.4(NCOR1):c.3338G>A (p.Arg1113Gln)	NCOR1 (R1113Q +1 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GBenign
Select item 3038527	NM_006311.4(NCOR1):c.3309C>T (p.Pro1103=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 716462	NM_006311.4(NCOR1):c.3249G>A (p.Val1083=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign
Select item 777135	NM_006311.4(NCOR1):c.2745C>T (p.Leu915=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign
Select item 3033586	NM_006311.4(NCOR1):c.2744T>G (p.Leu915Arg)	NCOR1 (L822R +2 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 710459	NM_006311.4(NCOR1):c.2513G>C (p.Gly838Ala)	NCOR1 (G838A +2 more)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 3055775	NM_006311.4(NCOR1):c.2445C>T (p.Pro815=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3055358	NM_006311.4(NCOR1):c.2366G>C (p.Ser789Thr)	NCOR1 (S696T +2 more)	Single nucleotide variant (missense variant)	NCOR1-related disorder	GLikely benign
Select item 3042406	NM_006311.4(NCOR1):c.2250G>A (p.Ala750=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3034508	NM_006311.4(NCOR1):c.2058T>C (p.Thr686=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GLikely benign
Select item 3049993	NM_006311.4(NCOR1):c.1488G>A (p.Gly496=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3049594	NM_006311.4(NCOR1):c.1352+10A>G	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder	GLikely benign
Select item 789340	NM_006311.4(NCOR1):c.1352+8A>G	NCOR1	Single nucleotide variant (intron variant)	NCOR1-related disorder +1 more	GBenign
Select item 3039988	NM_006311.4(NCOR1):c.768T>C (p.Gly256=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3052795	NM_006311.4(NCOR1):c.675T>A (p.Pro225=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder	GBenign
Select item 3052555	NM_006311.4(NCOR1):c.180G>A (p.Gln60=)	NCOR1	Single nucleotide variant (synonymous variant +1 more)	NCOR1-related disorder	GBenign
Select item 2647506	NM_006311.4(NCOR1):c.148G>A (p.Val50Met)	NCOR1 (V50M)	Single nucleotide variant (missense variant +1 more)	NCOR1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 712853	NM_006311.4(NCOR1):c.96C>T (p.Thr32=)	NCOR1	Single nucleotide variant (synonymous variant)	NCOR1-related disorder +1 more	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 41