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Items: 38

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NAPSA
(A416P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G411E)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G409V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(L408V)
Single nucleotide variant
(missense variant)
not provided
GBenign
NAPSA
(R404G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G357C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G331A)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(L330F)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G311R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(I303T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(L288P)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G277D)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(G270R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(E263K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(A256V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(V250M)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(Y243C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
Single nucleotide variant
(synonymous variant)
not provided
GBenign
NAPSA
(G231R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(M203I)
Single nucleotide variant
(missense variant)
Myoepithelial tumor
GUncertain significance
NAPSA
(D184G)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(H182Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(A170S)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(E152K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(R145W)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(Q140L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(A138V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(E81V)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(Y73C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(V68I)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(F67C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(K64R)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(A58T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(E52Q)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(R39K)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(R38C)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(I27T)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
NAPSA
(P15L)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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