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Items: 29

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASB15
(L237F)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASB15
(L247Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(A250T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(E286K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(G287R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(S300P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(R305Q)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASB15
(Q319H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(I342N)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(D348E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(V358I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(G373V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ASB15
(N391S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(L398V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(N407S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(R417H)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(L435F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(G439A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(F458S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(F458L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(I463T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(K477R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(V494L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(C511R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(R528C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(A558V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASB15
(V560M)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASB15
(A568P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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