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Items: 83

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZXDC
(P839R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V826I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(D823E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(E804K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V792I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(Q790R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(Q786R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A782E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P772S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(G767E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(C766Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(H758R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(H758N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(E749D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(G732R)
Single nucleotide variant
(3 prime UTR variant +1 more)
not specified
GUncertain significance
ZXDC
(Q683R)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ZXDC
(Q675R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P663L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P653S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A650G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(N649K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P646R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(T645I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P640S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(N630S)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ZXDC
(P624L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(D623N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(S605N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V601M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(G585R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(S580N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(S547F)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V542I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(G536E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(S529L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A522V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(T507I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(R479C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(R478W)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A470V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(K465Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P449L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V443L)
Single nucleotide variant
(missense variant +1 more)
not specified
GLikely benign
ZXDC
(C426R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V422M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(R350Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(F301L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(H290R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V272A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(E271D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(S266G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(K260R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A257T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A218V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(P207S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A185V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(P180R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(T172M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(Q166L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(Q166P)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(A160T)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(A160S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(Q134R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(P121L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(S106G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937463, ZXDC
(V102D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(Q94E)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(A87V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(V81G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC
(L78V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(D68V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(D68Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(P63L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(E57A)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(G56V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(L42M)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(R38C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(R26Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZXDC, LOC129937464
(G22D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(P21L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(G18D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(A5V)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
LOC129937464, ZXDC
(P4L)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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