Related gene-specific medical variations for Gene (Select 91392) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258430	NM_001134442.3(ZNF502):c.242G>C (p.Gly81Ala)	LOC126806664, ZNF502 (G81A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196228	NM_001134442.3(ZNF502):c.49T>G (p.Cys17Gly)	LOC126806664, ZNF502 (C17G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196227	NM_001134442.3(ZNF502):c.358G>A (p.Val120Ile)	LOC126806664, ZNF502 (V120I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196226	NM_001134442.3(ZNF502):c.350G>A (p.Arg117His)	LOC126806664, ZNF502 (R117H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3196225	NM_001134442.3(ZNF502):c.275A>C (p.Glu92Ala)	LOC126806664, ZNF502 (E92A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559394	NM_001134442.3(ZNF502):c.461C>T (p.Ser154Phe)	LOC126806664, ZNF502 (S154F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550522	NM_001134442.3(ZNF502):c.220G>C (p.Glu74Gln)	LOC126806664, ZNF502 (E74Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532912	NM_001134442.3(ZNF502):c.339C>A (p.Ser113Arg)	LOC126806664, ZNF502 (S113R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532340	NM_001134442.3(ZNF502):c.181T>C (p.Cys61Arg)	LOC126806664, ZNF502 (C61R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510320	NM_001134442.3(ZNF502):c.11T>C (p.Met4Thr)	LOC126806664, ZNF502 (M4T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410630	NM_001134442.3(ZNF502):c.349C>T (p.Arg117Cys)	LOC126806664, ZNF502 (R117C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance