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Items: 32

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZNF540, ZNF571
+1 more
(Q603P)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(Q590H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(P585S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R569H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(S568G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(E559Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R550K)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R541C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(Q521K)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF571, ZNF571-AS1
+1 more
(E519K)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R485H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(G480V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(C476R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(H465P)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(I412V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(G387A)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R374C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(F373L)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(E339G)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(H269Q)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(C256R)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(Y251C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(G235V)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(Y182C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(P180S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(Q156H)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R130Q)
Single nucleotide variant
(non-coding transcript variant +2 more)
Inborn genetic diseases
GLikely benign
ZNF540, ZNF571
+1 more
(K93I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(R76C)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(M73I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(M35I)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
ZNF540, ZNF571
+1 more
(L5S)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
GUncertain significance
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