"Ambry Genetics"[submitter] AND "ZNF821"[gene] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2614581	NM_001201552.2(ZNF821):c.1199A>T (p.Lys400Met)	ZNF821 (K250M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2298869	NM_001201552.2(ZNF821):c.1154A>G (p.Gln385Arg)	ZNF821 (Q235R +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2480569	NM_001201552.2(ZNF821):c.1131A>T (p.Leu377Phe)	ZNF821 (L227F +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2364099	NM_001201552.2(ZNF821):c.734G>A (p.Arg245His)	ZNF821 (R95H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2601584	NM_001201552.2(ZNF821):c.641G>T (p.Gly214Val)	ZNF821 (G214V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2268221	NM_001201552.2(ZNF821):c.629T>A (p.Val210Asp)	ZNF821 (V210D +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592331	NM_001201552.2(ZNF821):c.553G>A (p.Ala185Thr)	ZNF821 (A185T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2309521	NM_001201552.2(ZNF821):c.460G>C (p.Val154Leu)	ZNF821 (V154L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2535481	NM_001201552.2(ZNF821):c.400A>G (p.Ile134Val)	ZNF821 (I134V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592784	NM_001201552.2(ZNF821):c.305A>C (p.Glu102Ala)	ZNF821 (E60A +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2623896	NM_001201552.2(ZNF821):c.133A>G (p.Ile45Val)	ZNF821 (I45V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2494143	NM_001201552.2(ZNF821):c.83C>T (p.Ala28Val)	ZNF821 (A28V)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance