"Ambry Genetics"[submitter] AND "ZNF273"[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2356701	NM_021148.3(ZNF273):c.8C>G (p.Ser3Cys)	ZNF273 (S3C)	Single nucleotide variant (5 prime UTR variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2209539	NM_021148.3(ZNF273):c.290A>T (p.Asn97Ile)	ZNF273 (N32I +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2367985	NM_021148.3(ZNF273):c.332G>A (p.Cys111Tyr)	ZNF273 (C111Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2221413	NM_021148.3(ZNF273):c.425A>G (p.Glu142Gly)	ZNF273 (E45G +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2344249	NM_021148.3(ZNF273):c.644G>A (p.Cys215Tyr)	ZNF273 (C150Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379527	NM_021148.3(ZNF273):c.710A>G (p.Lys237Arg)	ZNF273 (K237R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2242121	NM_021148.3(ZNF273):c.717T>G (p.Cys239Trp)	ZNF273 (C142W +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332665	NM_021148.3(ZNF273):c.732C>A (p.Asn244Lys)	ZNF273 (N179K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2617719	NM_021148.3(ZNF273):c.752A>T (p.Lys251Ile)	ZNF273 (K154I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2544244	NM_021148.3(ZNF273):c.818A>G (p.Gln273Arg)	ZNF273 (Q176R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2226594	NM_021148.3(ZNF273):c.848T>G (p.Ile283Ser)	ZNF273 (I186S +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2276223	NM_021148.3(ZNF273):c.943A>G (p.Thr315Ala)	ZNF273 (T250A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2518038	NM_021148.3(ZNF273):c.977G>C (p.Gly326Ala)	ZNF273 (G229A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2599244	NM_021148.3(ZNF273):c.1099A>G (p.Ile367Val)	ZNF273 (I367V +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2371691	NM_021148.3(ZNF273):c.1159T>G (p.Ser387Ala)	ZNF273 (S290A +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2293016	NM_021148.3(ZNF273):c.1211G>A (p.Cys404Tyr)	ZNF273 (C339Y +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2493156	NM_021148.3(ZNF273):c.1228G>C (p.Ala410Pro)	ZNF273 (A313P +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2332366	NM_021148.3(ZNF273):c.1337C>T (p.Thr446Ile)	ZNF273 (T349I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2538835	NM_021148.3(ZNF273):c.1505C>A (p.Thr502Asn)	ZNF273 (T502N +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2587970	NM_021148.3(ZNF273):c.1517G>A (p.Arg506Lys)	ZNF273 (R506K +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475447	NM_021148.3(ZNF273):c.1520T>C (p.Ile507Thr)	ZNF273 (I410T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2247981	NM_021148.3(ZNF273):c.1685G>T (p.Arg562Ile)	ZNF273 (R497I +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 22