U.S. flag

An official website of the United States government

Format
Items per page
Sort by
Choose Destination

Search results

Items: 24

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOTCH2
(N2466del)
Microsatellite
(inframe_deletion)
not provided
GUncertain significance
NOTCH2
(A2188T)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+2 more
GUncertain significance
NOTCH2
(R2105Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
(S2070R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH2
(T1808fs)
Duplication
(frameshift variant)
not provided
GLikely pathogenic
NOTCH2
(A1775V)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH2
(R1578C)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+1 more
GUncertain significance
NOTCH2
(R1567W)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
(L1559V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
(E1488K)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+1 more
GUncertain significance
NOTCH2
(H1390R)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+3 more
GUncertain significance
NOTCH2
(R1372W)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+2 more
GUncertain significance
NOTCH2
(R1365H)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
Single nucleotide variant
(synonymous variant)
not provided
GUncertain significance
NOTCH2
(R1231P)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH2
Single nucleotide variant
(intron variant)
not provided
GUncertain significance
NOTCH2
(G1130S)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+2 more
GUncertain significance
NOTCH2
(I1107V)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
(G1005E)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
NOTCH2
(P939L)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
NOTCH2
(R869Q)
Single nucleotide variant
(missense variant)
Hajdu-Cheney syndrome
+1 more
GUncertain significance
NOTCH2
(T782I)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH2
(D746E)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
NOTCH2
(P229H)
Single nucleotide variant
(missense variant)
Alagille syndrome due to a NOTCH2 point mutation
+2 more
GUncertain significance
Format
Items per page
Sort by
Choose Destination