Related gene-specific medical variations for Gene (Select 147948) - ClinVar

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Links from Gene

Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258784	NM_001320371.4(ZNF582):c.1439A>G (p.Asn480Ser)	LOC126862939, ZNF582 (N480S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258782	NM_001320371.4(ZNF582):c.1336A>G (p.Thr446Ala)	LOC126862939, ZNF582 (T446A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258781	NM_001320371.4(ZNF582):c.710A>G (p.Asn237Ser)	LOC126862939, ZNF582 (N237S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3258780	NM_001320371.4(ZNF582):c.1195G>C (p.Val399Leu)	LOC126862939, ZNF582 (V399L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258779	NM_001320371.4(ZNF582):c.898G>C (p.Val300Leu)	LOC126862939, ZNF582 (V300L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196933	NM_001320371.4(ZNF582):c.716G>A (p.Gly239Asp)	LOC126862939, ZNF582 (G239D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196932	NM_001320371.4(ZNF582):c.575T>G (p.Ile192Ser)	LOC126862939, ZNF582 (I192S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196929	NM_001320371.4(ZNF582):c.1484T>G (p.Leu495Arg)	LOC126862939, ZNF582 (L495R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196926	NM_001320371.4(ZNF582):c.1399G>A (p.Val467Ile)	LOC126862939, ZNF582 (V467I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196924	NM_001320371.4(ZNF582):c.1049A>G (p.Gln350Arg)	LOC126862939, ZNF582 (Q350R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3058896	NM_001320371.4(ZNF582):c.1290G>A (p.Lys430=)	LOC126862939, ZNF582	Single nucleotide variant (synonymous variant)	ZNF582-related disorder	GBenign
Select item 3040476	NM_001320371.4(ZNF582):c.1533T>C (p.Asn511=)	LOC126862939, ZNF582	Single nucleotide variant (synonymous variant)	ZNF582-related disorder	GBenign
Select item 3033172	NM_001320371.4(ZNF582):c.1179A>G (p.Lys393=)	LOC126862939, ZNF582	Single nucleotide variant (synonymous variant)	ZNF582-related disorder	GLikely benign
Select item 2650560	NM_001320371.4(ZNF582):c.603T>C (p.Cys201=)	LOC126862939, ZNF582	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2617858	NM_001320371.4(ZNF582):c.1449T>A (p.Asn483Lys)	LOC126862939, ZNF582 (N483K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605075	NM_001320371.4(ZNF582):c.738G>T (p.Gln246His)	LOC126862939, ZNF582 (Q246H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556629	NM_001320371.4(ZNF582):c.1442T>C (p.Ile481Thr)	LOC126862939, ZNF582 (I481T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522855	NM_001320371.4(ZNF582):c.1207G>A (p.Ala403Thr)	LOC126862939, ZNF582 (A403T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462817	NM_001320371.4(ZNF582):c.1252A>G (p.Thr418Ala)	LOC126862939, ZNF582 (T418A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457031	NM_001320371.4(ZNF582):c.1379T>C (p.Leu460Ser)	LOC126862939, ZNF582 (L460S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398720	NM_001320371.4(ZNF582):c.1268A>G (p.Tyr423Cys)	LOC126862939, ZNF582 (Y423C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302616	NM_001320371.4(ZNF582):c.732A>T (p.Gln244His)	LOC126862939, ZNF582 (Q244H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285992	NM_001320371.4(ZNF582):c.1327G>A (p.Val443Ile)	LOC126862939, ZNF582 (V443I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2279102	NM_001320371.4(ZNF582):c.1478C>T (p.Pro493Leu)	LOC126862939, ZNF582 (P493L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 102451	NM_001320371.4(ZNF582):c.1034G>A (p.Gly345Glu)	LOC126862939, ZNF582 (G345E)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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Links from Gene

Items: 25