"Ambry Genetics"[submitter] AND "LOC126862922"[gene] - ClinVar - NCBI

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Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2516601	NM_001136499.2(ZNF841):c.2756C>T (p.Thr919Ile)	LOC126862922, ZNF841 (T803I +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2244091	NM_001136499.2(ZNF841):c.2698G>A (p.Ala900Thr)	LOC126862922, ZNF841 (A901T +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2409294	NM_001136499.2(ZNF841):c.2665C>T (p.Arg889Cys)	LOC126862922, ZNF841 (R773C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297880	NM_001136499.2(ZNF841):c.2578C>T (p.Arg860Trp)	LOC126862922, ZNF841 (R744W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2204091	NM_001136499.2(ZNF841):c.2450G>T (p.Gly817Val)	LOC126862922, ZNF841 (G817V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516616	NM_001136499.2(ZNF841):c.2434C>G (p.Gln812Glu)	LOC126862922, ZNF841 (Q696E +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2295264	NM_001136499.2(ZNF841):c.2419A>G (p.Ile807Val)	LOC126862922, ZNF841 (I691V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2351639	NM_001136499.2(ZNF841):c.2414G>A (p.Arg805His)	LOC126862922, ZNF841 (R806H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2400179	NM_001136499.2(ZNF841):c.2413C>T (p.Arg805Cys)	LOC126862922, ZNF841 (R805C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2268222	NM_001136499.2(ZNF841):c.2338C>T (p.Leu780Phe)	LOC126862922, ZNF841 (L781F +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2390456	NM_001136499.2(ZNF841):c.1861G>A (p.Gly621Arg)	LOC126862922, ZNF841 (G622R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2470437	NM_001136499.2(ZNF841):c.1850G>A (p.Arg617Gln)	ZNF841, LOC126862922 (R617Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2204058	NM_001136499.2(ZNF841):c.1820T>C (p.Ile607Thr)	ZNF841, LOC126862922 (I491T +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523503	NM_001136499.2(ZNF841):c.1720T>C (p.Cys574Arg)	LOC126862922, ZNF841 (C574R +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance