"Ambry Genetics"[submitter] AND "ADAMTS9"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3268028	NM_182920.2(ADAMTS9):c.5794G>A (p.Val1932Met)	ADAMTS9 (V1932M +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 2364593	NM_182920.2(ADAMTS9):c.5717C>T (p.Pro1906Leu)	ADAMTS9 (P1878L +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 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 2228657	NM_182920.2(ADAMTS9):c.5617C>A (p.Arg1873Ser)	ADAMTS9 (R1873S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268071	NM_182920.2(ADAMTS9):c.5587T>C (p.Cys1863Arg)	ADAMTS9 (C1863R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228501	NM_182920.2(ADAMTS9):c.5551G>A (p.Glu1851Lys)	ADAMTS9 (E1823K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292134	NM_182920.2(ADAMTS9):c.5431G>A (p.Asp1811Asn)	ADAMTS9, LOC126806704 (D1783N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242855	NM_182920.2(ADAMTS9):c.5396A>G (p.Asn1799Ser)	ADAMTS9, LOC126806704 (N1771S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 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 2075979	NM_182920.2(ADAMTS9):c.5239G>A (p.Gly1747Ser)	ADAMTS9, LOC126806704 (G1719S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 1586718	NM_182920.2(ADAMTS9):c.5191T>C (p.Tyr1731His)	ADAMTS9, LOC126806704 (Y1703H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
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 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 2291627	NM_182920.2(ADAMTS9):c.5140T>A (p.Leu1714Ile)	ADAMTS9, LOC126806704 (L1686I +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 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 3267947	NM_182920.2(ADAMTS9):c.4916G>T (p.Cys1639Phe)	ADAMTS9 (C1611F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212136	NM_182920.2(ADAMTS9):c.4829A>G (p.Gln1610Arg)	ADAMTS9 (Q1610R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209821	NM_182920.2(ADAMTS9):c.4811G>A (p.Arg1604His)	ADAMTS9 (R1576H +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 2185418	NM_182920.2(ADAMTS9):c.4810C>T (p.Arg1604Cys)	ADAMTS9 (R1604C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2385128	NM_182920.2(ADAMTS9):c.4802C>T (p.Pro1601Leu)	ADAMTS9 (P1573L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341294	NM_182920.2(ADAMTS9):c.4799G>A (p.Arg1600Gln)	ADAMTS9 (R1572Q +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 2312452	NM_182920.2(ADAMTS9):c.4751A>G (p.Asp1584Gly)	ADAMTS9 (D1584G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2287147	NM_182920.2(ADAMTS9):c.4707G>T (p.Lys1569Asn)	ADAMTS9 (K1541N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2377200	NM_182920.2(ADAMTS9):c.4579G>A (p.Gly1527Arg)	ADAMTS9, ADAMTS9-AS1 (G1499R +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 1535005	NM_182920.2(ADAMTS9):c.4562A>T (p.His1521Leu)	ADAMTS9, ADAMTS9-AS1 (H1493L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
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 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 2224240	NM_182920.2(ADAMTS9):c.4324G>A (p.Asp1442Asn)	ADAMTS9 (D1414N +1 more)	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 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 3268038	NM_182920.2(ADAMTS9):c.4220T>C (p.Val1407Ala)	ADAMTS9 (V1379A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227738	NM_182920.2(ADAMTS9):c.4169A>G (p.Asn1390Ser)	ADAMTS9 (N1362S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2408013	NM_182920.2(ADAMTS9):c.4055T>G (p.Val1352Gly)	ADAMTS9 (V1324G +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 2316130	NM_182920.2(ADAMTS9):c.3823C>T (p.Arg1275Trp)	ADAMTS9 (R1247W +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 2479185	NM_182920.2(ADAMTS9):c.3665G>A (p.Cys1222Tyr)	ADAMTS9 (C1222Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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 2392431	NM_182920.2(ADAMTS9):c.3607C>T (p.Arg1203Trp)	ADAMTS9 (R1175W +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 2239255	NM_182920.2(ADAMTS9):c.3575C>A (p.Thr1192Asn)	ADAMTS9 (T1164N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225712	NM_182920.2(ADAMTS9):c.3560G>A (p.Arg1187Gln)	ADAMTS9 (R1159Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2456989	NM_182920.2(ADAMTS9):c.3530G>A (p.Ser1177Asn)	ADAMTS9 (S1149N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1879584	NM_182920.2(ADAMTS9):c.3525G>C (p.Arg1175Ser)	ADAMTS9 (R1147S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 1478731	NM_182920.2(ADAMTS9):c.3503C>T (p.Pro1168Leu)	ADAMTS9 (P1168L +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 2221049	NM_182920.2(ADAMTS9):c.3473A>G (p.Gln1158Arg)	ADAMTS9 (Q1130R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2200862	NM_182920.2(ADAMTS9):c.3349G>A (p.Gly1117Arg)	ADAMTS9 (G1089R +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2316856	NM_182920.2(ADAMTS9):c.3344C>A (p.Pro1115His)	ADAMTS9 (P1087H +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 3268093	NM_182920.2(ADAMTS9):c.3317C>T (p.Pro1106Leu)	ADAMTS9 (P1078L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2226255	NM_182920.2(ADAMTS9):c.3299T>C (p.Met1100Thr)	ADAMTS9 (M1100T +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 2329007	NM_182920.2(ADAMTS9):c.3249A>C (p.Glu1083Asp)	ADAMTS9 (E1055D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305780	NM_182920.2(ADAMTS9):c.3218A>C (p.Lys1073Thr)	ADAMTS9 (K1073T +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 2384845	NM_182920.2(ADAMTS9):c.3083G>A (p.Arg1028Gln)	ADAMTS9 (R1000Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239818	NM_182920.2(ADAMTS9):c.3043G>A (p.Gly1015Ser)	ADAMTS9 (G987S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402016	NM_182920.2(ADAMTS9):c.3005G>A (p.Arg1002His)	ADAMTS9 (R974H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268049	NM_182920.2(ADAMTS9):c.2999G>A (p.Gly1000Asp)	ADAMTS9 (G972D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387088	NM_182920.2(ADAMTS9):c.2993C>T (p.Thr998Met)	ADAMTS9 (T970M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 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 1432726	NM_182920.2(ADAMTS9):c.2867G>A (p.Arg956His)	ADAMTS9 (R928H +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	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 2482781	NM_182920.2(ADAMTS9):c.2778C>G (p.His926Gln)	ADAMTS9 (H898Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359840	NM_182920.2(ADAMTS9):c.2758C>T (p.Arg920Trp)	ADAMTS9 (R892W +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	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 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 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 2242278	NM_182920.2(ADAMTS9):c.2594G>A (p.Arg865His)	ADAMTS9 (R837H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326398	NM_182920.2(ADAMTS9):c.2588A>G (p.Asp863Gly)	ADAMTS9 (D835G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268060	NM_182920.2(ADAMTS9):c.2587G>C (p.Asp863His)	ADAMTS9 (D863H +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 2268505	NM_182920.2(ADAMTS9):c.2554C>G (p.Gln852Glu)	ADAMTS9 (Q852E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2405266	NM_182920.2(ADAMTS9):c.2129C>A (p.Pro710His)	ADAMTS9 (P682H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251566	NM_182920.2(ADAMTS9):c.2084A>G (p.Asn695Ser)	ADAMTS9 (N667S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
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 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 2391242	NM_182920.2(ADAMTS9):c.2008A>G (p.Asn670Asp)	ADAMTS9 (N642D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267958	NM_182920.2(ADAMTS9):c.1954G>A (p.Glu652Lys)	ADAMTS9 (E652K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332692	NM_182920.2(ADAMTS9):c.1933C>G (p.Gln645Glu)	ADAMTS9 (Q617E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237030	NM_182920.2(ADAMTS9):c.1933C>A (p.Gln645Lys)	ADAMTS9 (Q617K +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 2270835	NM_182920.2(ADAMTS9):c.1862A>G (p.Lys621Arg)	ADAMTS9 (K621R +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 2408655	NM_182920.2(ADAMTS9):c.1829C>T (p.Thr610Ile)	ADAMTS9 (T582I +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 2273046	NM_182920.2(ADAMTS9):c.1778G>A (p.Ser593Asn)	ADAMTS9 (S593N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2341044	NM_182920.2(ADAMTS9):c.1756G>A (p.Val586Met)	ADAMTS9 (V558M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3268082	NM_182920.2(ADAMTS9):c.1720T>C (p.Tyr574His)	ADAMTS9 (Y546H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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