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Items: 17

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ZFP57
(R517T +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(T438N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(T491S +1 more)
Single nucleotide variant
(missense variant)
ZFP57-related condition
+4 more
GConflicting classifications of pathogenicity
ZFP57
(L375I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(V428A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(S322N +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(S371C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(I243V +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(S190C +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(R251H +1 more)
Single nucleotide variant
(missense variant)
Diabetes mellitus, transient neonatal, 1
+1 more
GUncertain significance
ZFP57
(R250H +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
ZFP57
(C180Y +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(A157P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(S82P +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(E62K +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(T113A +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
ZFP57
(L25I +1 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
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