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Items: 16

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADH1C
(R313H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(V295L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(I292F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(L280R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(V208A)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADH1C
(V208I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(K186E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(A164V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(T146S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(L124P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(P120R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(G118A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(I73V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(V64A)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ADH1C
(H52L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ADH1C
(E17A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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