"Ambry Genetics"[submitter] AND "ZNF140"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2330118	NM_003440.4(ZNF140):c.37A>G (p.Ile13Val)	ZNF140 (I13V)	Single nucleotide variant (5 prime UTR variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2291097	NM_003440.4(ZNF140):c.211G>A (p.Val71Met)	ZNF140 (V71M)	Single nucleotide variant (5 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2328567	NM_003440.4(ZNF140):c.271A>G (p.Lys91Glu)	ZNF891, ZNF140 (K91E)	Single nucleotide variant (3 prime UTR variant +3 more)	Inborn genetic diseases	GUncertain significance
Select item 2208274	NM_003440.4(ZNF140):c.413G>A (p.Arg138Lys)	ZNF140, ZNF891 (R10K +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291553	NM_003440.4(ZNF140):c.424G>A (p.Val142Ile)	ZNF140, ZNF891 (V14I +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2357132	NM_003440.4(ZNF140):c.713C>T (p.Thr238Met)	ZNF891, ZNF140 (T135M +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2385547	NM_003440.4(ZNF140):c.746A>T (p.Glu249Val)	ZNF891, ZNF140 (E121V +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304458	NM_003440.4(ZNF140):c.835G>A (p.Gly279Ser)	ZNF891, ZNF140 (G279S +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2391848	NM_003440.4(ZNF140):c.872A>T (p.His291Leu)	ZNF891, ZNF140 (H188L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2332509	NM_003440.4(ZNF140):c.876G>T (p.Gln292His)	ZNF891, ZNF140 (Q164H +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2412455	NM_003440.4(ZNF140):c.932G>T (p.Arg311Leu)	ZNF891, ZNF140 (R183L +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2408480	NM_003440.4(ZNF140):c.934C>T (p.Arg312Cys)	ZNF891, ZNF140 (R184C +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2387946	NM_003440.4(ZNF140):c.935G>A (p.Arg312His)	ZNF140, ZNF891 (R184H +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2365368	NM_003440.4(ZNF140):c.983C>G (p.Pro328Arg)	ZNF891, ZNF140 (P200R +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2522110	NM_003440.4(ZNF140):c.1003A>G (p.Arg335Gly)	ZNF140, ZNF891 (R335G +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2287566	NM_003440.4(ZNF140):c.1048A>G (p.Ile350Val)	ZNF140, ZNF891 (I350V +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2519695	NM_003440.4(ZNF140):c.1334A>C (p.Asn445Thr)	ZNF140, ZNF891 (N317T +2 more)	Single nucleotide variant (3 prime UTR variant +1 more)	Inborn genetic diseases	GUncertain significance