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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOTCH1
Single nucleotide variant
(intron variant)
not provided
+1 more
GConflicting classifications of pathogenicity
NOTCH1
(G1612S)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH1
(G1342C)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH1
(P1337R)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
+3 more
GUncertain significance
NOTCH1
(G1331R)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
NOTCH1
Single nucleotide variant
(splice acceptor variant)
not provided
GLikely pathogenic
NOTCH1
(D869N)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
NOTCH1
(P837R)
Single nucleotide variant
(missense variant)
Adams-Oliver syndrome 5
+3 more
GUncertain significance
NOTCH1
(N764S)
Single nucleotide variant
(missense variant)
Familial thoracic aortic aneurysm and aortic dissection
+3 more
GConflicting classifications of pathogenicity
NOTCH1
(Y670D)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH1
(P593L)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
+3 more
GUncertain significance
NOTCH1
(G317S)
Single nucleotide variant
(missense variant)
Adams-Oliver syndrome 5
+3 more
GConflicting classifications of pathogenicity
NOTCH1
(G251S)
Single nucleotide variant
(missense variant)
Aortic valve disease 1
+2 more
GConflicting classifications of pathogenicity
NOTCH1
(S225W)
Single nucleotide variant
(missense variant)
not provided
+3 more
GConflicting classifications of pathogenicity
NOTCH1
(C206Y)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH1
(N151S)
Single nucleotide variant
(missense variant)
not provided
+3 more
GUncertain significance
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