ADAMTS9[gene] and "single gene"[properties] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1294798	NM_182920.2(ADAMTS9):c.5798G>A (p.Arg1933Gln)	ADAMTS9 (R1905Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
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 2031785	NM_182920.2(ADAMTS9):c.5782A>C (p.Thr1928Pro)	ADAMTS9 (T1928P +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 791933	NM_182920.2(ADAMTS9):c.5760A>G (p.Gly1920=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 789164	NM_182920.2(ADAMTS9):c.5742A>G (p.Lys1914=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1546394	NM_182920.2(ADAMTS9):c.5734G>A (p.Val1912Ile)	ADAMTS9 (V1884I +1 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
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 1227721	NM_182920.2(ADAMTS9):c.5718+220C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1556219	NM_182920.2(ADAMTS9):c.5718+19G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
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 2980270	NM_182920.2(ADAMTS9):c.5691T>C (p.Tyr1897=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 1910792	NM_182920.2(ADAMTS9):c.5658T>C (p.Thr1886=)	ADAMTS9	Single nucleotide variant (synonymous 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 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 1265324	NM_182920.2(ADAMTS9):c.5614-48A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232527	NM_182920.2(ADAMTS9):c.5614-210G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 1410113	NM_182920.2(ADAMTS9):c.5584G>T (p.Asp1862Tyr)	ADAMTS9 (D1834Y +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2143033	NM_182920.2(ADAMTS9):c.5580C>T (p.Ala1860=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 1275247	NM_182920.2(ADAMTS9):c.5065-158G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236708	NM_182920.2(ADAMTS9):c.5065-189C>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1175412	NM_182920.2(ADAMTS9):c.5064+180T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1909330	NM_182920.2(ADAMTS9):c.5050G>A (p.Gly1684Ser)	ADAMTS9 (G1656S +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1287404	NM_182920.2(ADAMTS9):c.5022C>G (p.Asp1674Glu)	ADAMTS9 (D1646E +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
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 1902443	NM_182920.2(ADAMTS9):c.5019G>A (p.Arg1673=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 746403	NM_182920.2(ADAMTS9):c.4932C>T (p.Thr1644=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 778839	NM_182920.2(ADAMTS9):c.4920C>T (p.Ser1640=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 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 2632360	NM_182920.2(ADAMTS9):c.4870-2A>G	ADAMTS9	Single nucleotide variant (splice acceptor variant)	ADAMTS9-related disorder	GUncertain significance
Select item 1262094	NM_182920.2(ADAMTS9):c.4870-145A>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 specified +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 specified +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 716446	NM_182920.2(ADAMTS9):c.4789G>A (p.Val1597Met)	ADAMTS9 (V1569M +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 782987	NM_182920.2(ADAMTS9):c.4788C>T (p.Asp1596=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2096577	NM_182920.2(ADAMTS9):c.4783T>A (p.Cys1595Ser)	ADAMTS9 (C1567S +1 more)	Single nucleotide variant (missense variant)	not provided	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 1558609	NM_182920.2(ADAMTS9):c.4743G>T (p.Val1581=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3036245	NM_182920.2(ADAMTS9):c.4735A>G (p.Lys1579Glu)	ADAMTS9 (K1551E +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related disorder	GLikely benign
Select item 2059604	NM_182920.2(ADAMTS9):c.4717G>A (p.Glu1573Lys)	ADAMTS9 (E1545K +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2653945	NM_182920.2(ADAMTS9):c.4716C>T (p.Gly1572=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2071140	NM_182920.2(ADAMTS9):c.4699-4A>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1256705	NM_182920.2(ADAMTS9):c.4699-80G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1183919	NM_182920.2(ADAMTS9):c.4356+153A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 774301	NM_182920.2(ADAMTS9):c.4356+4C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GLikely benign
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 1651412	NM_182920.2(ADAMTS9):c.4287C>T (p.Pro1429=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 1353100	NM_182920.2(ADAMTS9):c.4246C>T (p.Arg1416Trp)	ADAMTS9 (R1388W +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1253274	NM_182920.2(ADAMTS9):c.4222G>A (p.Val1408Ile)	ADAMTS9 (V1380I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
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 1258973	NM_182920.2(ADAMTS9):c.4180-18del	ADAMTS9	Deletion (intron variant)	not provided	GBenign
Select item 1273366	NM_182920.2(ADAMTS9):c.4180-25G>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178391	NM_182920.2(ADAMTS9):c.4180-59G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226052	NM_182920.2(ADAMTS9):c.4179+18G>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1987818	NM_182920.2(ADAMTS9):c.4179+11A>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 2633398	NM_182920.2(ADAMTS9):c.4108A>G (p.Ile1370Val)	ADAMTS9 (I1342V +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related disorder	GUncertain significance
Select item 3040758	NM_182920.2(ADAMTS9):c.4092C>T (p.Asn1364=)	ADAMTS9	Single nucleotide variant (synonymous variant)	ADAMTS9-related disorder	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 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 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 1639744	NM_182920.2(ADAMTS9):c.4038C>T (p.Gly1346=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1510869	NM_182920.2(ADAMTS9):c.4018-7T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1281071	NM_182920.2(ADAMTS9):c.4018-84T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275428	NM_182920.2(ADAMTS9):c.4018-185T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245912	NM_182920.2(ADAMTS9):c.4017+58A>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 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 2635954	NM_182920.2(ADAMTS9):c.3949C>T (p.Arg1317Trp)	ADAMTS9 (R1289W +1 more)	Single nucleotide variant (missense variant)	ADAMTS9-related disorder	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 1266552	NM_182920.2(ADAMTS9):c.3819C>T (p.Ile1273=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 781711	NM_182920.2(ADAMTS9):c.3780C>T (p.Thr1260=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 2653946	NM_182920.2(ADAMTS9):c.3591T>C (p.Thr1197=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 1256919	NM_182920.2(ADAMTS9):c.3580-42A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1232121	NM_182920.2(ADAMTS9):c.3579+52T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 2011467	NM_182920.2(ADAMTS9):c.3552C>T (p.Thr1184=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2096640	NM_182920.2(ADAMTS9):c.3529A>C (p.Ser1177Arg)	ADAMTS9 (S1177R +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

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