"Ambry Genetics"[submitter] AND "ZNF473"[gene] - ClinVar

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Items: 40

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3196041	NM_015428.4(ZNF473):c.100A>G (p.Thr34Ala)	ZNF473 (T22A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196046	NM_015428.4(ZNF473):c.148C>T (p.Pro50Ser)	ZNF473 (P38S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302357	NM_015428.4(ZNF473):c.218C>T (p.Thr73Ile)	ZNF473 (T73I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2470329	NM_015428.4(ZNF473):c.343G>A (p.Ala115Thr)	ZNF473 (A103T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556311	NM_015428.4(ZNF473):c.469A>G (p.Ser157Gly)	ZNF473 (S145G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196051	NM_015428.4(ZNF473):c.487T>A (p.Ser163Thr)	ZNF473 (S163T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2517784	NM_015428.4(ZNF473):c.560G>A (p.Arg187Lys)	ZNF473 (R175K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219779	NM_015428.4(ZNF473):c.565G>A (p.Glu189Lys)	ZNF473 (E189K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340559	NM_015428.4(ZNF473):c.566A>G (p.Glu189Gly)	ZNF473 (E177G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389275	NM_015428.4(ZNF473):c.661A>C (p.Ser221Arg)	ZNF473 (S209R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216420	NM_015428.4(ZNF473):c.792C>G (p.Phe264Leu)	ZNF473 (F252L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219665	NM_015428.4(ZNF473):c.905G>A (p.Ser302Asn)	ZNF473 (S302N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530661	NM_015428.4(ZNF473):c.929A>T (p.His310Leu)	ZNF473 (H310L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2268358	NM_015428.4(ZNF473):c.944C>A (p.Thr315Lys)	ZNF473 (T303K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374996	NM_015428.4(ZNF473):c.970G>A (p.Glu324Lys)	ZNF473 (E324K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196042	NM_015428.4(ZNF473):c.1030C>T (p.Arg344Trp)	ZNF473 (R332W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216256	NM_015428.4(ZNF473):c.1031G>A (p.Arg344Gln)	ZNF473 (R344Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3196043	NM_015428.4(ZNF473):c.1039T>C (p.Tyr347His)	ZNF473 (Y347H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476647	NM_015428.4(ZNF473):c.1064C>T (p.Thr355Ile)	ZNF473 (T343I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2544245	NM_015428.4(ZNF473):c.1190A>G (p.His397Arg)	ZNF473 (H397R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258956	NM_015428.4(ZNF473):c.1208A>T (p.Tyr403Phe)	ZNF473 (Y391F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302983	NM_015428.4(ZNF473):c.1222C>T (p.Arg408Cys)	ZNF473 (R396C +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2339647	NM_015428.4(ZNF473):c.1249A>T (p.Thr417Ser)	ZNF473 (T417S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196044	NM_015428.4(ZNF473):c.1269G>C (p.Arg423Ser)	ZNF473 (R423S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491089	NM_015428.4(ZNF473):c.1352G>A (p.Arg451Gln)	ZNF473 (R439Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196045	NM_015428.4(ZNF473):c.1381T>C (p.Cys461Arg)	ZNF473 (C449R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597987	NM_015428.4(ZNF473):c.1393G>A (p.Val465Ile)	ZNF473 (V465I +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2615220	NM_015428.4(ZNF473):c.1439T>G (p.Ile480Ser)	ZNF473 (I468S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2358310	NM_015428.4(ZNF473):c.1561G>A (p.Gly521Arg)	ZNF473 (G521R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196047	NM_015428.4(ZNF473):c.1579G>T (p.Gly527Cys)	ZNF473 (G515C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513922	NM_015428.4(ZNF473):c.1630T>C (p.Phe544Leu)	ZNF473 (F544L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2332965	NM_015428.4(ZNF473):c.1691G>A (p.Cys564Tyr)	ZNF473 (C552Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361495	NM_015428.4(ZNF473):c.1813C>T (p.Arg605Trp)	ZNF473 (R593W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215209	NM_015428.4(ZNF473):c.1919A>C (p.His640Pro)	ZNF473 (H628P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616034	NM_015428.4(ZNF473):c.1948G>A (p.Glu650Lys)	ZNF473 (E638K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196048	NM_015428.4(ZNF473):c.2081G>A (p.Arg694Gln)	ZNF473 (R694Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374148	NM_015428.4(ZNF473):c.2102C>T (p.Pro701Leu)	ZNF473 (P689L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3196049	NM_015428.4(ZNF473):c.2211G>C (p.Lys737Asn)	ZNF473 (K737N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326846	NM_015428.4(ZNF473):c.2218G>A (p.Gly740Ser)	ZNF473 (G740S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2253161	NM_015428.4(ZNF473):c.2462A>G (p.Lys821Arg)	ZNF473 (K821R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 40