ClinVar for Gene (Select 56999) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3078765	NM_182920.2(ADAMTS9):c.889G>T (p.Val297Phe)	ADAMTS9 (V297F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078757	NM_182920.2(ADAMTS9):c.694C>T (p.His232Tyr)	ADAMTS9 (H232Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078753	NM_182920.2(ADAMTS9):c.674C>T (p.Thr225Ile)	ADAMTS9 (T225I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078728	NM_182920.2(ADAMTS9):c.5261A>G (p.Tyr1754Cys)	ADAMTS9, LOC126806704 (Y1726C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078725	NM_182920.2(ADAMTS9):c.5207C>A (p.Pro1736His)	ADAMTS9, LOC126806704 (P1708H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078715	NM_182920.2(ADAMTS9):c.5159A>G (p.Lys1720Arg)	ADAMTS9, LOC126806704 (K1720R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078707	NM_182920.2(ADAMTS9):c.4933G>A (p.Gly1645Arg)	ADAMTS9 (G1617R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078683	NM_182920.2(ADAMTS9):c.46G>A (p.Asp16Asn)	ADAMTS9, ADAMTS9-AS2 (D16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078662	NM_182920.2(ADAMTS9):c.4310A>G (p.His1437Arg)	ADAMTS9 (H1437R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078660	NM_182920.2(ADAMTS9):c.4276G>C (p.Asp1426His)	ADAMTS9 (D1398H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078644	NM_182920.2(ADAMTS9):c.4001C>A (p.Thr1334Asn)	ADAMTS9 (T1306N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078640	NM_182920.2(ADAMTS9):c.3845A>G (p.Tyr1282Cys)	ADAMTS9 (Y1282C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078626	NM_182920.2(ADAMTS9):c.3509C>A (p.Ala1170Asp)	ADAMTS9 (A1170D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078617	NM_182920.2(ADAMTS9):c.3483A>C (p.Glu1161Asp)	ADAMTS9 (E1161D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078610	NM_182920.2(ADAMTS9):c.3329C>A (p.Ser1110Tyr)	ADAMTS9 (S1082Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078605	NM_182920.2(ADAMTS9):c.3296C>A (p.Ser1099Tyr)	ADAMTS9 (S1071Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078598	NM_182920.2(ADAMTS9):c.3112A>G (p.Thr1038Ala)	ADAMTS9 (T1010A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078586	NM_182920.2(ADAMTS9):c.2887G>A (p.Ala963Thr)	ADAMTS9 (A963T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078579	NM_182920.2(ADAMTS9):c.2789C>A (p.Pro930His)	ADAMTS9 (P902H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078565	NM_182920.2(ADAMTS9):c.2720A>G (p.Glu907Gly)	ADAMTS9 (E907G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078557	NM_182920.2(ADAMTS9):c.2587G>A (p.Asp863Asn)	ADAMTS9 (D835N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078555	NM_182920.2(ADAMTS9):c.253G>A (p.Ala85Thr)	ADAMTS9, ADAMTS9-AS2 (A85T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078552	NM_182920.2(ADAMTS9):c.2054G>A (p.Arg685Gln)	ADAMTS9 (R657Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078540	NM_182920.2(ADAMTS9):c.1858C>G (p.Pro620Ala)	ADAMTS9 (P620A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078520	NM_182920.2(ADAMTS9):c.1640A>G (p.Asn547Ser)	ADAMTS9 (N547S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078516	NM_182920.2(ADAMTS9):c.1636G>A (p.Val546Ile)	ADAMTS9 (V518I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078500	NM_182920.2(ADAMTS9):c.1305G>T (p.Glu435Asp)	ADAMTS9 (E407D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3078491	NM_182920.2(ADAMTS9):c.1094A>G (p.Lys365Arg)	ADAMTS9 (K365R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062713	GRCh37/hg19 3p14.2-13(chr3:62188399-71663248)x1	ADAMTS9, ARL6IP5 +24 more	Copy number loss	not specified	GPathogenic
Select item 3052234	NM_182920.2(ADAMTS9):c.5430C>A (p.Arg1810=)	ADAMTS9, LOC126806704	Single nucleotide variant (synonymous variant)	ADAMTS9-related condition	GLikely benign
Select item 3040758	NM_182920.2(ADAMTS9):c.4092C>T (p.Asn1364=)	ADAMTS9	Single nucleotide variant (synonymous variant)	ADAMTS9-related condition	GLikely benign
Select item 3036245	NM_182920.2(ADAMTS9):c.4735A>G (p.Lys1579Glu)	ADAMTS9 (K1551E +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related condition	GLikely benign
Select item 3034840	NM_182920.2(ADAMTS9):c.2505C>T (p.Ala835=)	ADAMTS9	Single nucleotide variant (synonymous variant)	ADAMTS9-related condition	GLikely benign
Select item 3034475	NM_182920.2(ADAMTS9):c.2184A>C (p.Gly728=)	ADAMTS9	Single nucleotide variant (synonymous variant)	ADAMTS9-related condition	GLikely benign
Select item 3020701	NM_182920.2(ADAMTS9):c.3475-17del	ADAMTS9	Deletion (intron variant)	not provided	GBenign
Select item 3011280	NM_182920.2(ADAMTS9):c.1305G>A (p.Glu435=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2992740	NM_182920.2(ADAMTS9):c.5020G>T (p.Asp1674Tyr)	ADAMTS9 (D1646Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2980270	NM_182920.2(ADAMTS9):c.5691T>C (p.Tyr1897=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2979038	NM_182920.2(ADAMTS9):c.4015G>T (p.Ala1339Ser)	ADAMTS9 (A1339S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2978260	NM_182920.2(ADAMTS9):c.4560G>A (p.Arg1520=)	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2964161	NM_182920.2(ADAMTS9):c.5171G>A (p.Arg1724Gln)	ADAMTS9, LOC126806704 (R1696Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2955573	NM_182920.2(ADAMTS9):c.1464-14G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2894323	NM_182920.2(ADAMTS9):c.1054-9T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2891178	NM_182920.2(ADAMTS9):c.1995C>T (p.Asn665=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2887054	NM_182920.2(ADAMTS9):c.2389+7T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2882919	NM_182920.2(ADAMTS9):c.1857-9C>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2865216	NM_182920.2(ADAMTS9):c.4913C>T (p.Ser1638Leu)	ADAMTS9 (S1610L +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2861006	NM_182920.2(ADAMTS9):c.2990A>G (p.Asn997Ser)	ADAMTS9 (N969S +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2860584	NM_182920.2(ADAMTS9):c.733G>A (p.Gly245Arg)	ADAMTS9 (G245R)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2853490	NM_182920.2(ADAMTS9):c.5477G>A (p.Ser1826Asn)	ADAMTS9, LOC126806704 (S1826N +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2809051	NM_182920.2(ADAMTS9):c.516+2T>C	ADAMTS9, ADAMTS9-AS2	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 2809035	NM_182920.2(ADAMTS9):c.1857-15T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2789886	NM_182920.2(ADAMTS9):c.2039-18A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2778681	NM_182920.2(ADAMTS9):c.4083C>T (p.Tyr1361=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2778070	NM_182920.2(ADAMTS9):c.407A>T (p.Gln136Leu)	ADAMTS9, ADAMTS9-AS2 (Q136L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2777953	NM_182920.2(ADAMTS9):c.4049G>A (p.Arg1350Gln)	ADAMTS9 (R1322Q +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2764903	NM_182920.2(ADAMTS9):c.2793T>A (p.Cys931Ter)	ADAMTS9 (C903* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2753919	NM_182920.2(ADAMTS9):c.2763G>T (p.Leu921=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2752039	NM_182920.2(ADAMTS9):c.3355-6_3355-4del	ADAMTS9	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2728510	NM_182920.2(ADAMTS9):c.2687-10T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2724457	NM_182920.2(ADAMTS9):c.818C>T (p.Thr273Met)	ADAMTS9 (T273M)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2721005	NM_182920.2(ADAMTS9):c.1548C>T (p.Asn516=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2716721	NM_182920.2(ADAMTS9):c.579A>T (p.Glu193Asp)	ADAMTS9 (E193D)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 2712811	NM_182920.2(ADAMTS9):c.5646C>G (p.Gly1882=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2653948	NM_182920.2(ADAMTS9):c.2475T>C (p.Ala825=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2653947	NM_182920.2(ADAMTS9):c.3396G>A (p.Val1132=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2653946	NM_182920.2(ADAMTS9):c.3591T>C (p.Thr1197=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2653945	NM_182920.2(ADAMTS9):c.4716C>T (p.Gly1572=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2637014	NM_182920.2(ADAMTS9):c.2209G>A (p.Ala737Thr)	ADAMTS9 (A709T +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related condition	GUncertain significance
Select item 2635954	NM_182920.2(ADAMTS9):c.3949C>T (p.Arg1317Trp)	ADAMTS9 (R1289W +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related condition	GUncertain significance
Select item 2633398	NM_182920.2(ADAMTS9):c.4108A>G (p.Ile1370Val)	ADAMTS9 (I1342V +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related condition	GUncertain significance
Select item 2632360	NM_182920.2(ADAMTS9):c.4870-2A>G	ADAMTS9	Single nucleotide variant (splice acceptor variant)	ADAMTS9-related condition	GUncertain significance
Select item 2623046	NM_182920.2(ADAMTS9):c.5632C>G (p.Leu1878Val)	ADAMTS9 (L1878V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616653	NM_182920.2(ADAMTS9):c.1548C>A (p.Asn516Lys)	ADAMTS9 (N488K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2616271	NM_182920.2(ADAMTS9):c.3596G>A (p.Gly1199Glu)	ADAMTS9 (G1171E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614510	NM_182920.2(ADAMTS9):c.4513G>T (p.Ala1505Ser)	ADAMTS9, ADAMTS9-AS1 (A1505S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611198	NM_182920.2(ADAMTS9):c.2985A>C (p.Glu995Asp)	ADAMTS9 (E967D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2610529	NM_182920.2(ADAMTS9):c.580C>G (p.Gln194Glu)	ADAMTS9 (Q194E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2605737	NM_182920.2(ADAMTS9):c.697A>G (p.Ser233Gly)	ADAMTS9 (S233G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2603948	NM_182920.2(ADAMTS9):c.1159C>A (p.Leu387Ile)	ADAMTS9 (L387I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598644	NM_182920.2(ADAMTS9):c.5335G>A (p.Val1779Met)	ADAMTS9, LOC126806704 (V1779M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598058	NM_182920.2(ADAMTS9):c.1916C>T (p.Thr639Met)	ADAMTS9 (T611M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594822	NM_182920.2(ADAMTS9):c.1492G>A (p.Glu498Lys)	ADAMTS9 (E498K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594444	NM_182920.2(ADAMTS9):c.4496C>T (p.Pro1499Leu)	ADAMTS9, ADAMTS9-AS1 (P1499L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594432	NM_182920.2(ADAMTS9):c.182A>T (p.Glu61Val)	ADAMTS9, ADAMTS9-AS2 (E61V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592979	NM_182920.2(ADAMTS9):c.2009A>G (p.Asn670Ser)	ADAMTS9 (N642S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2566590	NM_182920.2(ADAMTS9):c.5729G>A (p.Arg1910Gln)	ADAMTS9 (R1882Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562142	NM_182920.2(ADAMTS9):c.5177C>T (p.Thr1726Ile)	ADAMTS9, LOC126806704 (T1698I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547532	NM_182920.2(ADAMTS9):c.1826A>G (p.Lys609Arg)	ADAMTS9 (K581R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545601	NM_182920.2(ADAMTS9):c.1661G>A (p.Arg554Gln)	ADAMTS9 (R526Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540896	NM_182920.2(ADAMTS9):c.3670A>G (p.Thr1224Ala)	ADAMTS9 (T1224A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539195	NM_182920.2(ADAMTS9):c.1433G>A (p.Cys478Tyr)	ADAMTS9 (C450Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533442	NM_182920.2(ADAMTS9):c.4267G>C (p.Glu1423Gln)	ADAMTS9 (E1423Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525903	NM_182920.2(ADAMTS9):c.5681A>G (p.Gln1894Arg)	ADAMTS9 (Q1866R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522429	NM_182920.2(ADAMTS9):c.2729A>G (p.Gln910Arg)	ADAMTS9 (Q910R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2516202	NM_182920.2(ADAMTS9):c.4781G>A (p.Arg1594His)	ADAMTS9 (R1594H +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2513827	NM_182920.2(ADAMTS9):c.3634G>A (p.Glu1212Lys)	ADAMTS9 (E1212K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508446	NM_182920.2(ADAMTS9):c.4994C>G (p.Pro1665Arg)	ADAMTS9 (P1637R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495646	NM_182920.2(ADAMTS9):c.2677C>A (p.Pro893Thr)	ADAMTS9 (P893T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482781	NM_182920.2(ADAMTS9):c.2778C>G (p.His926Gln)	ADAMTS9 (H898Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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