"Ambry Genetics"[submitter] AND "ZNF267"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3194778	NM_003414.6(ZNF267):c.23A>C (p.Asp8Ala)	ZNF267 (D8A)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2255996	NM_003414.6(ZNF267):c.140T>G (p.Val47Gly)	ZNF267 (V15G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623677	NM_003414.6(ZNF267):c.149C>T (p.Pro50Leu)	ZNF267 (P50L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484161	NM_003414.6(ZNF267):c.204G>C (p.Glu68Asp)	ZNF267 (E68D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2623216	NM_003414.6(ZNF267):c.264G>C (p.Glu88Asp)	ZNF267 (E88D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549187	NM_003414.6(ZNF267):c.347G>C (p.Arg116Thr)	ZNF267 (R116T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194779	NM_003414.6(ZNF267):c.402T>A (p.Phe134Leu)	ZNF267 (F102L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2316026	NM_003414.6(ZNF267):c.502G>A (p.Val168Ile)	ZNF267 (V168I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298621	NM_003414.6(ZNF267):c.524T>A (p.Leu175His)	ZNF267 (L143H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194781	NM_003414.6(ZNF267):c.646T>C (p.Tyr216His)	ZNF267 (Y184H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194782	NM_003414.6(ZNF267):c.656A>G (p.Asn219Ser)	ZNF267 (N187S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194783	NM_003414.6(ZNF267):c.659A>C (p.Asn220Thr)	ZNF267 (N220T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194784	NM_003414.6(ZNF267):c.679C>G (p.Gln227Glu)	ZNF267 (Q227E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194785	NM_003414.6(ZNF267):c.689G>A (p.Ser230Asn)	ZNF267 (S198N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2346233	NM_003414.6(ZNF267):c.761T>A (p.Leu254His)	ZNF267 (L254H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338673	NM_003414.6(ZNF267):c.763C>G (p.Gln255Glu)	ZNF267 (Q223E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2596093	NM_003414.6(ZNF267):c.770T>C (p.Met257Thr)	ZNF267 (M257T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2269832	NM_003414.6(ZNF267):c.941T>C (p.Ile314Thr)	ZNF267 (I314T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2216693	NM_003414.6(ZNF267):c.998A>G (p.His333Arg)	ZNF267 (H333R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2319228	NM_003414.6(ZNF267):c.1033A>G (p.Thr345Ala)	ZNF267 (T313A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369684	NM_003414.6(ZNF267):c.1036G>A (p.Glu346Lys)	ZNF267 (E314K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2374101	NM_003414.6(ZNF267):c.1121A>G (p.Asp374Gly)	ZNF267 (D374G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366619	NM_003414.6(ZNF267):c.1124C>A (p.Thr375Asn)	ZNF267 (T343N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525242	NM_003414.6(ZNF267):c.1138T>A (p.Tyr380Asn)	ZNF267 (Y380N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2512833	NM_003414.6(ZNF267):c.1186A>G (p.Ile396Val)	ZNF267 (I364V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3194777	NM_003414.6(ZNF267):c.1376C>T (p.Thr459Ile)	ZNF267 (T427I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401499	NM_003414.6(ZNF267):c.1382A>G (p.Glu461Gly)	ZNF267 (E461G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395561	NM_003414.6(ZNF267):c.1423C>T (p.Arg475Cys)	ZNF267 (R443C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545026	NM_003414.6(ZNF267):c.1457A>G (p.His486Arg)	ZNF267 (H486R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328608	NM_003414.6(ZNF267):c.1676A>G (p.Tyr559Cys)	ZNF267 (Y559C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377758	NM_003414.6(ZNF267):c.1723C>A (p.Pro575Thr)	ZNF267 (P543T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2364978	NM_003414.6(ZNF267):c.1867C>T (p.Arg623Trp)	ZNF267 (R591W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212404	NM_003414.6(ZNF267):c.2035C>T (p.Arg679Trp)	ZNF267 (R647W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2264138	NM_003414.6(ZNF267):c.2141G>C (p.Arg714Thr)	ZNF267 (R682T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256687	NM_003414.6(ZNF267):c.2154T>G (p.Cys718Trp)	ZNF267 (C686W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2527671	NM_003414.6(ZNF267):c.2182A>G (p.Arg728Gly)	ZNF267 (R696G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 36