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Items: 33

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZWILCH
(F12I)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
ZWILCH
(L17F)
Single nucleotide variant
(5 prime UTR variant +1 more)
not provided
GBenign
ZWILCH
(P48T)
Single nucleotide variant
(5 prime UTR variant +2 more)
not specified
GUncertain significance
ZWILCH
(A106S)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance
ZWILCH
(L136F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(T158R +1 more)
Single nucleotide variant
(missense variant)
not provided
GLikely benign
ZWILCH
(Y168C +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
Single nucleotide variant
(synonymous variant)
not provided
GLikely benign
ZWILCH
(H80Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
Single nucleotide variant
(intron variant)
not provided
GBenign
ZWILCH
(S230Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(E254K +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(R166G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(D205G +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(D219Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(R220H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(S221F +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(S221Y +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(R338C +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZWILCH
(R229L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(T257I +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(R379H +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(S278N +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(G299V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(I301V +1 more)
Single nucleotide variant
(missense variant)
not specified
GLikely benign
ZWILCH
(P339L +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(I481M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(L390P +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(Q415E +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(V533M +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
(P553A +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZWILCH
Single nucleotide variant
(intron variant)
not provided
GBenign
ZWILCH
(L455V +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
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