"Ambry Genetics"[submitter] AND "ZNF613"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3258914	NM_001031721.4(ZNF613):c.76G>A (p.Gly26Ser)	ZNF613 (G26S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2538942	NM_001031721.4(ZNF613):c.127A>G (p.Asn43Asp)	ZNF613 (N43D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197200	NM_001031721.4(ZNF613):c.242A>C (p.Lys81Thr)	ZNF613 (K81T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299717	NM_001031721.4(ZNF613):c.248T>C (p.Val83Ala)	ZNF613 (V47A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384143	NM_001031721.4(ZNF613):c.308G>T (p.Cys103Phe)	ZNF613 (C67F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258912	NM_001031721.4(ZNF613):c.311A>G (p.His104Arg)	ZNF613 (H68R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552951	NM_001031721.4(ZNF613):c.321T>G (p.Asn107Lys)	ZNF613 (N71K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341552	NM_001031721.4(ZNF613):c.538G>A (p.Glu180Lys)	ZNF613 (E144K +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2411814	NM_001031721.4(ZNF613):c.541G>T (p.Gly181Cys)	ZNF613 (G181C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2305081	NM_001031721.4(ZNF613):c.643A>G (p.Lys215Glu)	ZNF613 (K179E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383504	NM_001031721.4(ZNF613):c.673G>A (p.Val225Ile)	ZNF613 (V189I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615439	NM_001031721.4(ZNF613):c.808C>G (p.Arg270Gly)	ZNF613 (R234G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392396	NM_001031721.4(ZNF613):c.808C>T (p.Arg270Cys)	ZNF613 (R234C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358038	NM_001031721.4(ZNF613):c.823C>T (p.Leu275Phe)	ZNF613 (L239F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197201	NM_001031721.4(ZNF613):c.862T>C (p.Tyr288His)	ZNF613 (Y252H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197202	NM_001031721.4(ZNF613):c.904C>T (p.Arg302Trp)	ZNF613 (R266W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463419	NM_001031721.4(ZNF613):c.905G>A (p.Arg302Gln)	ZNF613 (R266Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616763	NM_001031721.4(ZNF613):c.924A>C (p.Arg308Ser)	ZNF613 (R272S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601387	NM_001031721.4(ZNF613):c.948T>A (p.His316Gln)	ZNF613 (H316Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395644	NM_001031721.4(ZNF613):c.1039A>C (p.Thr347Pro)	ZNF613 (T347P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197197	NM_001031721.4(ZNF613):c.1068A>C (p.Lys356Asn)	ZNF613 (K320N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526747	NM_001031721.4(ZNF613):c.1078A>G (p.Asn360Asp)	ZNF613 (N360D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288025	NM_001031721.4(ZNF613):c.1103G>T (p.Gly368Val)	ZNF613 (G332V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238248	NM_001031721.4(ZNF613):c.1208A>G (p.Asn403Ser)	ZNF613 (N367S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2410658	NM_001031721.4(ZNF613):c.1258C>T (p.Arg420Cys)	ZNF613 (R384C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346699	NM_001031721.4(ZNF613):c.1303A>G (p.Lys435Glu)	ZNF613 (K435E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390376	NM_001031721.4(ZNF613):c.1344A>T (p.Arg448Ser)	ZNF613 (R412S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465595	NM_001031721.4(ZNF613):c.1436C>T (p.Thr479Ile)	ZNF613 (T443I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197198	NM_001031721.4(ZNF613):c.1448C>T (p.Pro483Leu)	ZNF613 (P447L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2271114	NM_001031721.4(ZNF613):c.1508G>A (p.Arg503Gln)	ZNF613 (R503Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3258913	NM_001031721.4(ZNF613):c.1530A>C (p.Arg510Ser)	ZNF613 (R510S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3197199	NM_001031721.4(ZNF613):c.1679G>A (p.Arg560His)	ZNF613 (R524H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212712	NM_001031721.4(ZNF613):c.1687A>C (p.Ile563Leu)	ZNF613 (I563L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303317	NM_001031721.4(ZNF613):c.1728G>C (p.Met576Ile)	ZNF613 (M540I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272783	NM_001031721.4(ZNF613):c.1765G>A (p.Ala589Thr)	ZNF613 (A553T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380716	NM_001031721.4(ZNF613):c.1766C>T (p.Ala589Val)	ZNF613 (A553V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 36