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

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Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3199666	NM_007157.4(ZXDB):c.19C>T (p.Leu7Phe)	ZXDB (L7F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293138	NM_007157.4(ZXDB):c.70G>A (p.Gly24Ser)	ZXDB (G24S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477811	NM_007157.4(ZXDB):c.119C>T (p.Pro40Leu)	ZXDB (P40L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199661	NM_007157.4(ZXDB):c.121A>C (p.Thr41Pro)	ZXDB (T41P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2552503	NM_007157.4(ZXDB):c.125G>A (p.Arg42His)	ZXDB (R42H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199662	NM_007157.4(ZXDB):c.151C>G (p.Gln51Glu)	ZXDB (Q51E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599526	NM_007157.4(ZXDB):c.200G>C (p.Arg67Pro)	ZXDB (R67P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270252	NM_007157.4(ZXDB):c.203G>A (p.Gly68Asp)	ZXDB (G68D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345194	NM_007157.4(ZXDB):c.222G>C (p.Leu74Phe)	ZXDB (L74F)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 3260199	NM_007157.4(ZXDB):c.244A>G (p.Ser82Gly)	ZXDB (S82G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2343992	NM_007157.4(ZXDB):c.257G>T (p.Gly86Val)	ZXDB (G86V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310907	NM_007157.4(ZXDB):c.323G>C (p.Gly108Ala)	LOC130068356, ZXDB (G108A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549192	NM_007157.4(ZXDB):c.328G>A (p.Gly110Ser)	LOC130068356, ZXDB (G110S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549193	NM_007157.4(ZXDB):c.337G>A (p.Ala113Thr)	LOC130068356, ZXDB (A113T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2398585	NM_007157.4(ZXDB):c.351G>T (p.Leu117Phe)	LOC130068356, ZXDB (L117F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292982	NM_007157.4(ZXDB):c.371G>T (p.Gly124Val)	LOC130068356, ZXDB (G124V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2401239	NM_007157.4(ZXDB):c.401C>T (p.Ala134Val)	LOC130068356, ZXDB (A134V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405810	NM_007157.4(ZXDB):c.418A>T (p.Thr140Ser)	LOC130068356, ZXDB (T140S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2385115	NM_007157.4(ZXDB):c.425T>A (p.Leu142Gln)	LOC130068356, ZXDB (L142Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357198	NM_007157.4(ZXDB):c.434G>A (p.Arg145His)	LOC130068356, ZXDB (R145H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199669	NM_007157.4(ZXDB):c.540T>G (p.Phe180Leu)	LOC130068356, ZXDB (F180L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260195	NM_007157.4(ZXDB):c.541G>C (p.Glu181Gln)	LOC130068356, ZXDB (E181Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361472	NM_007157.4(ZXDB):c.547G>C (p.Gly183Arg)	LOC130068356, ZXDB (G183R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367043	NM_007157.4(ZXDB):c.580G>C (p.Ala194Pro)	LOC130068356, ZXDB (A194P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199670	NM_007157.4(ZXDB):c.590C>T (p.Pro197Leu)	LOC130068356, ZXDB (P197L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199671	NM_007157.4(ZXDB):c.616G>A (p.Gly206Arg)	ZXDB (G206R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2354089	NM_007157.4(ZXDB):c.659A>C (p.His220Pro)	LOC130068357, ZXDB (H220P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199672	NM_007157.4(ZXDB):c.662C>T (p.Pro221Leu)	LOC130068357, ZXDB (P221L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2315809	NM_007157.4(ZXDB):c.665G>A (p.Gly222Asp)	LOC130068357, ZXDB (G222D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542490	NM_007157.4(ZXDB):c.683C>G (p.Pro228Arg)	LOC130068357, ZXDB (P228R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2526962	NM_007157.4(ZXDB):c.725C>T (p.Ala242Val)	LOC130068357, ZXDB (A242V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199673	NM_007157.4(ZXDB):c.755C>T (p.Pro252Leu)	LOC130068357, ZXDB (P252L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199674	NM_007157.4(ZXDB):c.782C>T (p.Pro261Leu)	LOC130068357, ZXDB (P261L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260201	NM_007157.4(ZXDB):c.796C>T (p.Pro266Ser)	LOC130068357, ZXDB (P266S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346988	NM_007157.4(ZXDB):c.799G>T (p.Gly267Cys)	LOC130068357, ZXDB (G267C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603837	NM_007157.4(ZXDB):c.836G>C (p.Gly279Ala)	LOC130068357, ZXDB (G279A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507688	NM_007157.4(ZXDB):c.895C>A (p.Gln299Lys)	ZXDB (Q299K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199657	NM_007157.4(ZXDB):c.1010C>A (p.Pro337Gln)	ZXDB (P337Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199658	NM_007157.4(ZXDB):c.1069G>A (p.Gly357Ser)	ZXDB (G357S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304989	NM_007157.4(ZXDB):c.1113G>C (p.Glu371Asp)	ZXDB (E371D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199660	NM_007157.4(ZXDB):c.1138A>G (p.Ser380Gly)	ZXDB (S380G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260198	NM_007157.4(ZXDB):c.1348G>A (p.Gly450Ser)	ZXDB (G450S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219888	NM_007157.4(ZXDB):c.1543G>A (p.Val515Met)	ZXDB (V515M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2219924	NM_007157.4(ZXDB):c.1556C>T (p.Ala519Val)	ZXDB (A519V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199663	NM_007157.4(ZXDB):c.1702A>G (p.Met568Val)	ZXDB (M568V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457821	NM_007157.4(ZXDB):c.1714C>A (p.His572Asn)	ZXDB (H572N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339078	NM_007157.4(ZXDB):c.1721T>C (p.Val574Ala)	ZXDB (V574A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199664	NM_007157.4(ZXDB):c.1754C>A (p.Ala585Glu)	ZXDB (A585E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260197	NM_007157.4(ZXDB):c.1810G>A (p.Asp604Asn)	ZXDB (D604N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199665	NM_007157.4(ZXDB):c.1819A>G (p.Ile607Val)	ZXDB (I607V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233457	NM_007157.4(ZXDB):c.1912G>A (p.Ala638Thr)	ZXDB (A638T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2246839	NM_007157.4(ZXDB):c.1922G>A (p.Ser641Asn)	ZXDB (S641N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357783	NM_007157.4(ZXDB):c.2035C>G (p.Leu679Val)	ZXDB (L679V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260193	NM_007157.4(ZXDB):c.2098A>G (p.Ser700Gly)	ZXDB (S700G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2290922	NM_007157.4(ZXDB):c.2101G>T (p.Val701Leu)	ZXDB (V701L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260194	NM_007157.4(ZXDB):c.2126T>C (p.Leu709Pro)	ZXDB (L709P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406412	NM_007157.4(ZXDB):c.2270C>T (p.Ala757Val)	ZXDB (A757V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3260196	NM_007157.4(ZXDB):c.2281G>A (p.Val761Ile)	ZXDB (V761I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463723	NM_007157.4(ZXDB):c.2329G>A (p.Gly777Arg)	ZXDB (G777R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199667	NM_007157.4(ZXDB):c.2369A>C (p.Glu790Ala)	ZXDB (E790A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 60