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Items: 29

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
WEE2, WEE2-AS1
(Y18H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(E21V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(E23D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(P55S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(S70L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(A96V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(E182Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(R200Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(I240T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(R242C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(R242H)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(S255L)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WEE2, WEE2-AS1
(Y276C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(H310N)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(K350R)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(G357R)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+1 more
GUncertain significance
WEE2, WEE2-AS1
(F369S)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(G379D)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(A384T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(P413A)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(V451I)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GLikely benign
WEE2-AS1, WEE2
(E454Q)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(E472K)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(N483K)
Single nucleotide variant
(non-coding transcript variant +1 more)
Inborn genetic diseases
GUncertain significance
WEE2-AS1, WEE2
(P523T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(G525V)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(S543T)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(K545E)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
WEE2, WEE2-AS1
(R563C)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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