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Items: 31

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADH1B
(L333R +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(K340E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(M297T +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(K324N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(R273H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(M267V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(Q260P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(V253A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(V291F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(C287S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(L241F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(M218I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(A238V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(N226K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(A182V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(K173N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(V209I +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADH1B
(P152S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(N146K +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ADH1B
(I173V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(S125L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(A124S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(R134S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(T123N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(N115K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(S69I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(P67L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(P107A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(P52L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B
(P52S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ADH1B, LOC126807122
(P31T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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