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Items: 51

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
SP4
(E11A)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
SP4
(E29K +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SP4
(E12Q +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SP4
(N15S +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
SP4
(Q86H +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(V93L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S90T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(P109L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(A121V +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S107L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(A135T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S146P +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S146F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(P148R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(G132R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(G144S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(P152S +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(A210T +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(V220I +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(Q244L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(T249A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(V237L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(L283F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S302F +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(T309A +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
SP4
(M1V +2 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
SP4
(S16L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(E43Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(T341A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(E352D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(A355V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(S375F +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(Q367H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(I403V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(Q411R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(P404A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(S424L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(F425C +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(Q113H +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(V159L +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(I477M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(I520V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(L209M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(T537A +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(V245I +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(I575V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(E300Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(A607T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(I335V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(G390V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
SP4
(A756T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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