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Items: 38

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZCCHC8
(K466Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(R459Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(T569A +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ZCCHC8
(A429V +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ZCCHC8
(N394H +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(G389V +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(E375Q +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(K590N +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ZCCHC8
(T339M +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GConflicting classifications of pathogenicity
ZCCHC8
(E497K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(P328L +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ZCCHC8
(N462D +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(D304N +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ZCCHC8
(R449Q +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
LOC130009053, ZCCHC8
(A276T +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ZCCHC8
(Q264P +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ZCCHC8
(T419I +3 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GUncertain significance
ZCCHC8
(P256S +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(L488F +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(R378G +3 more)
Single nucleotide variant
(missense variant)
not provided
+1 more
GUncertain significance
ZCCHC8
(D447N +3 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance
ZCCHC8
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
ZCCHC8
(G362E +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(G362R +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(N337K +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(V202L +3 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZCCHC8
(G134D +1 more)
Single nucleotide variant
(missense variant +2 more)
not specified
GUncertain significance
ZCCHC8
(K152E +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ZCCHC8
(P142L +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
ZCCHC8
(D87H)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZCCHC8
(D87N)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GConflicting classifications of pathogenicity
ZCCHC8
(L84W)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ZCCHC8
(A47V)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ZCCHC8
(E39K)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ZCCHC8
(K32R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZCCHC8
(K32Q)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZCCHC8
(E20K)
Single nucleotide variant
(missense variant +1 more)
not provided
+1 more
GUncertain significance
ZCCHC8
(L10I)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
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