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Links from Gene

Items: 38

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF326
(S113N)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(E112D)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(F95Y)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(R80G)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(N153S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(I295M +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(E332G +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(S94N +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(A254V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(G227R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(E4K)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
BARHL2, GBP1
+16 more
Copy number gain
not provided
GUncertain significance
GBP1, GBP2
+15 more
Copy number loss
not provided
GUncertain significance
ZNF326
(D573V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(G27S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(Y101C +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(P339S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(K401R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(I394T +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(R201Q +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(R200W +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(G250E +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(G279V +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(Y43C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(E197D +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(S131R)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(E557K +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(N228S +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
ZNF326
(N14S)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ZNF326
(K151R +2 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
MCOLN3, MIGA1
+97 more
Copy number loss
not specified
GPathogenic
GBP2, GBP4
+7 more
Copy number loss
not provided
GUncertain significance
AGL, AGMAT
+783 more
Copy number gain
Intellectual disability, mild
+1 more
GUncertain significance
ZNF326, LRRC8D
Copy number gain
not provided
GUncertain significance
CD34, CD46
+2014 more
Copy number gain
See cases
GPathogenic
GPATCH2, GPATCH3
+2014 more
Copy number gain
See cases
GPathogenic
ACADM, ADGRL2
+80 more
Copy number loss
See cases
GPathogenic
LINC01708, LINC01709
+549 more
Copy number gain
See cases
GPathogenic
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