Related gene-specific medical variations for Gene (Select 51042) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3197028	NM_015871.5(ZNF593):c.46G>T (p.Ala16Ser)	ZNF593, ZNF593OS (A16S)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3197027	NM_015871.5(ZNF593):c.110C>T (p.Pro37Leu)	ZNF593, ZNF593OS (P37L)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2597388	NM_015871.5(ZNF593):c.149A>C (p.Glu50Ala)	ZNF593, ZNF593OS (E50A)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2558043	NM_015871.5(ZNF593):c.214G>A (p.Asp72Asn)	ZNF593, ZNF593OS (D72N)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2511974	NM_015871.5(ZNF593):c.132G>C (p.Gln44His)	ZNF593, ZNF593OS (Q44H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2477439	NM_015871.5(ZNF593):c.142A>C (p.Asn48His)	ZNF593, ZNF593OS (N48H)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2381990	NM_015871.5(ZNF593):c.148G>A (p.Glu50Lys)	ZNF593, ZNF593OS (E50K)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2354851	NM_015871.5(ZNF593):c.250G>T (p.Asp84Tyr)	ZNF593, ZNF593OS (D84Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2313518	NM_015871.5(ZNF593):c.290A>G (p.Tyr97Cys)	ZNF593, ZNF593OS (Y97C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216029	NM_015871.5(ZNF593):c.94C>T (p.His32Tyr)	ZNF593, ZNF593OS (H32Y)	Single nucleotide variant (3 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2205534	NM_015871.5(ZNF593):c.367G>A (p.Val123Met)	ZNF593, ZNF593OS (V123M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance