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Items: 53

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ASCC2
(R506Q +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(A687V +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E490G +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R483H +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R479Q +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R617H +12 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(K496Q +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E432K +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(T407I +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R563L +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R401S +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(I559F +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(V389M +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(S368R +10 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R472L +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(K499R +7 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(K326R +6 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASCC2
(R479W +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(P351S +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(N284S +6 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ASCC2
(R283H +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(D340E +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(R456W +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(Y260C +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(D481Y +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(M385I +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(N210I +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E267G +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(T317M +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E307K +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(D229A +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(V292M +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(S302C +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(S264G +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(L256F +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(L282P +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E348K +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(G230V +6 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(E175K +5 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ASCC2
(L135V +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(L171V +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(K129N +5 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ASCC2
(D183G +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ASCC2
(F27L +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ASCC2
(T124A +4 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ASCC2
(N58D +3 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(R121Q +2 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(Y44H +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(E32K +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(R58H)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(A50T)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(Q31R)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ASCC2
(A26V)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
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