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Items: 84

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
BRAF
(S226T +4 more)
Single nucleotide variant
(missense variant)
LEOPARD syndrome 3
GUncertain significance
BRAF
Microsatellite
(intron variant)
LEOPARD syndrome 3
+8 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(synonymous variant)
Colorectal cancer
+8 more
GLikely benign
BRAF
Single nucleotide variant
(intron variant)
LEOPARD syndrome 3
+7 more
GLikely benign
BRAF
Single nucleotide variant
(synonymous variant +1 more)
LEOPARD syndrome 3
+7 more
GLikely benign
BRAF
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 1
+7 more
GLikely benign
BRAF
Deletion
(intron variant)
RASopathy
+7 more
GLikely benign
BRAF
(A42S)
Single nucleotide variant
(missense variant)
LEOPARD syndrome 3
+7 more
GUncertain significance
BRAF
(G9A)
Single nucleotide variant
(missense variant)
RASopathy
+8 more
GUncertain significance
BRAF
(I662V +7 more)
Single nucleotide variant
(missense variant +1 more)
RASopathy
+7 more
GUncertain significance
BRAF
Insertion
(intron variant)
RASopathy
+8 more
GBenign/Likely benign
BRAF, LOC126860202
(R266Q +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 1
+8 more
GUncertain significance
BRAF
(Y545H +7 more)
Single nucleotide variant
(missense variant)
Cardiofaciocutaneous syndrome 1
+7 more
GUncertain significance
BRAF
(S35N +2 more)
Single nucleotide variant
(missense variant +1 more)
Cardiofaciocutaneous syndrome 1
+8 more
GUncertain significance
BRAF
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 1
+8 more
GLikely benign
BRAF
Single nucleotide variant
(synonymous variant)
Noonan syndrome 1
+8 more
GLikely benign
BRAF
Single nucleotide variant
(synonymous variant)
Noonan syndrome 1
+7 more
GLikely benign
BRAF
Single nucleotide variant
(synonymous variant)
Cardiovascular phenotype
+9 more
GConflicting classifications of pathogenicity
BRAF
(A38P)
Single nucleotide variant
(missense variant)
LEOPARD syndrome 3
+8 more
GUncertain significance
BRAF, LOC129999507
Single nucleotide variant
(5 prime UTR variant)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(5 prime UTR variant)
LEOPARD syndrome 3
+1 more
GUncertain significance
BRAF, LOC126860202
(D318E +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF, LOC126860202
(Q268E +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
(S342P +5 more)
Single nucleotide variant
(missense variant +1 more)
Cardiofaciocutaneous syndrome 1
+7 more
GUncertain significance
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
LEOPARD syndrome 3
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
+2 more
GConflicting classifications of pathogenicity
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
(R136T +3 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
(E611G +7 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 7
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(synonymous variant)
Noonan syndrome 1
+9 more
GLikely benign
BRAF
(P402H +5 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+10 more
GUncertain significance
BRAF
Single nucleotide variant
(intron variant)
RASopathy
+8 more
GLikely benign
BRAF
(Y647C +7 more)
Single nucleotide variant
(missense variant)
Cardiofaciocutaneous syndrome 1
+6 more
GUncertain significance
BRAF
(G397D +5 more)
Single nucleotide variant
(missense variant +1 more)
LEOPARD syndrome 3
+3 more
GUncertain significance
BRAF
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 1
+8 more
GBenign/Likely benign
BRAF, LOC126860202
Single nucleotide variant
(synonymous variant)
RASopathy
+4 more
GConflicting classifications of pathogenicity
BRAF
(G106R +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GUncertain significance
BRAF
(V157I +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+3 more
GUncertain significance
BRAF
Single nucleotide variant
(synonymous variant +1 more)
not provided
+5 more
GConflicting classifications of pathogenicity
BRAF
Single nucleotide variant
(intron variant)
Noonan syndrome 1
+8 more
GLikely benign
BRAF
Single nucleotide variant
(intron variant)
RASopathy
+9 more
GBenign/Likely benign
BRAF
(R389H +4 more)
Single nucleotide variant
(missense variant +1 more)
Lung carcinoma
+7 more
GUncertain significance
BRAF
(R146Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Lung carcinoma
+7 more
GConflicting classifications of pathogenicity
BRAF, LOC126860202
Single nucleotide variant
(intron variant)
LEOPARD syndrome 3
+3 more
GConflicting classifications of pathogenicity
BRAF, LOC126860202
(I342V +4 more)
Single nucleotide variant
(missense variant)
RASopathy
GUncertain significance
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
LEOPARD syndrome 3
+1 more
GUncertain significance
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
LEOPARD syndrome 3
+1 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
Noonan syndrome 7
+1 more
GBenign
BRAF
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 1
+8 more
GBenign/Likely benign
BRAF, LOC126860202
Single nucleotide variant
(intron variant)
not specified
+8 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(intron variant)
Cardiofaciocutaneous syndrome 1
+8 more
GBenign/Likely benign
BRAF
(A712D +7 more)
Single nucleotide variant
(missense variant +1 more)
Cardio-facio-cutaneous syndrome
+9 more
GConflicting classifications of pathogenicity
BRAF
Single nucleotide variant
(3 prime UTR variant +1 more)
RASopathy
GLikely benign
BRAF
Single nucleotide variant
(5 prime UTR variant)
Noonan syndrome and Noonan-related syndrome
+4 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(intron variant)
not specified
+8 more
GBenign/Likely benign
BRAF
(E24D)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(synonymous variant +1 more)
RASopathy
GBenign
BRAF
Single nucleotide variant
(synonymous variant +1 more)
not specified
+10 more
GBenign/Likely benign
BRAF
(N581K +7 more)
Single nucleotide variant
(missense variant)
Cardio-facio-cutaneous syndrome
+6 more
GPathogenic/Likely pathogenic
BRAF
Single nucleotide variant
(intron variant)
not specified
+3 more
GConflicting classifications of pathogenicity
BRAF
(V413M +5 more)
Single nucleotide variant
(missense variant +1 more)
Cardiofaciocutaneous syndrome 1
+8 more
GUncertain significance
BRAF, LOC126860202
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(intron variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(5 prime UTR variant)
RASopathy
+4 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(synonymous variant +1 more)
RASopathy
GBenign
BRAF
Single nucleotide variant
(intron variant)
not specified
+8 more
GBenign/Likely benign
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
(L485S +7 more)
Single nucleotide variant
(missense variant)
RASopathy
GLikely pathogenic
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(intron variant)
not provided
+9 more
GBenign
BRAF
Single nucleotide variant
(synonymous variant +1 more)
RASopathy
GBenign
BRAF
(L245F +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome and Noonan-related syndrome
GPathogenic
BRAF
Single nucleotide variant
(synonymous variant +1 more)
Cardiovascular phenotype
+10 more
GBenign/Likely benign
BRAF
(E26D)
Single nucleotide variant
(missense variant)
not specified
+7 more
GBenign/Likely benign
BRAF
(D22N)
Single nucleotide variant
(missense variant)
RASopathy
GBenign
BRAF
Single nucleotide variant
(synonymous variant)
RASopathy
GBenign
BRAF
(T241P +4 more)
Single nucleotide variant
(missense variant)
Noonan syndrome 7
+7 more
GPathogenic/Likely pathogenic
BRAF
(T241M +4 more)
Single nucleotide variant
(missense variant)
LEOPARD syndrome 3
+9 more
GPathogenic/Likely pathogenic
BRAF
(D638E +7 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+7 more
GPathogenic/Likely pathogenic
BRAF
(Q257R +4 more)
Single nucleotide variant
(missense variant)
Cardio-facio-cutaneous syndrome
GPathogenic
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