"GeneDx"[submitter] AND "ADAMTS9"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 81

	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 1227721	NM_182920.2(ADAMTS9):c.5718+220C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
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 1245807	NM_182920.2(ADAMTS9):c.5521+204T>C	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228118	NM_182920.2(ADAMTS9):c.5521+161C>T	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251849	NM_182920.2(ADAMTS9):c.5521+159A>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264037	NM_182920.2(ADAMTS9):c.5521+99CACATTG[2]	ADAMTS9, LOC126806704	Microsatellite (intron variant)	not provided	GBenign
Select item 1247158	NM_182920.2(ADAMTS9):c.5521+54C>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222970	NM_182920.2(ADAMTS9):c.5388-38T>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263575	NM_182920.2(ADAMTS9):c.5388-39C>T	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275404	NM_182920.2(ADAMTS9):c.5293-38T>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251224	NM_182920.2(ADAMTS9):c.5219A>G (p.Lys1740Arg)	ADAMTS9, LOC126806704 (K1712R +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1281816	NM_182920.2(ADAMTS9):c.5198-25A>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1274295	NM_182920.2(ADAMTS9):c.5198-40G>A	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1225641	NM_182920.2(ADAMTS9):c.5198-82C>T	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1244533	NM_182920.2(ADAMTS9):c.5197+49G>T	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1234754	NM_182920.2(ADAMTS9):c.5197+49G>A	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227294	NM_182920.2(ADAMTS9):c.5197+13A>G	ADAMTS9, LOC126806704	Single nucleotide variant (intron variant)	not provided	GBenign
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 1287404	NM_182920.2(ADAMTS9):c.5022C>G (p.Asp1674Glu)	ADAMTS9 (D1646E +1 more)	Single nucleotide variant (missense 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 1262094	NM_182920.2(ADAMTS9):c.4870-145A>C	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 1286160	NM_182920.2(ADAMTS9):c.4698+76A>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1248560	NM_182920.2(ADAMTS9):c.4525-50C>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1266838	NM_182920.2(ADAMTS9):c.4525-75G>A	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229313	NM_182920.2(ADAMTS9):c.4524+81A>G	ADAMTS9-AS1, ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242995	NM_182920.2(ADAMTS9):c.4357-43A>G	ADAMTS9, ADAMTS9-AS1	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1262649	NM_182920.2(ADAMTS9):c.4357-48C>T	ADAMTS9, ADAMTS9-AS1	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 1253274	NM_182920.2(ADAMTS9):c.4222G>A (p.Val1408Ile)	ADAMTS9 (V1380I +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
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 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 1266552	NM_182920.2(ADAMTS9):c.3819C>T (p.Ile1273=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 1183300	NM_182920.2(ADAMTS9):c.3522G>A (p.Thr1174=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1229452	NM_182920.2(ADAMTS9):c.3354+157A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270743	NM_182920.2(ADAMTS9):c.3190-94A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279189	NM_182920.2(ADAMTS9):c.3189+168G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1182473	NM_182920.2(ADAMTS9):c.3189+139T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1224605	NM_182920.2(ADAMTS9):c.3025-214G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237786	NM_182920.2(ADAMTS9):c.3024+94C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242183	NM_182920.2(ADAMTS9):c.3024+86A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281923	NM_182920.2(ADAMTS9):c.2814-160T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265499	NM_182920.2(ADAMTS9):c.2687-15del	ADAMTS9	Deletion (intron variant)	not provided	GBenign
Select item 1267825	NM_182920.2(ADAMTS9):c.2389+94C>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227983	NM_182920.2(ADAMTS9):c.2389+89C>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282290	NM_182920.2(ADAMTS9):c.2389+61G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229605	NM_182920.2(ADAMTS9):c.2293+113A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1268834	NM_182920.2(ADAMTS9):c.2293+61C>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1288405	NM_182920.2(ADAMTS9):c.2176-89T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245871	NM_182920.2(ADAMTS9):c.2176-98T>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1260504	NM_182920.2(ADAMTS9):c.2175+100G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230358	NM_182920.2(ADAMTS9):c.1856+207A>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1278617	NM_182920.2(ADAMTS9):c.1856+76G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1245713	NM_182920.2(ADAMTS9):c.1711-83G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265160	NM_182920.2(ADAMTS9):c.1711-148C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281043	NM_182920.2(ADAMTS9):c.1710+112T>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283400	NM_182920.2(ADAMTS9):c.1605+61A>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1235239	NM_182920.2(ADAMTS9):c.1463+133dup	ADAMTS9	Duplication (intron variant)	not provided	GBenign
Select item 1275884	NM_182920.2(ADAMTS9):c.1463+149del	ADAMTS9	Deletion (intron variant)	not provided	GBenign
Select item 1265899	NM_182920.2(ADAMTS9):c.1210+47A>G	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1270808	NM_182920.2(ADAMTS9):c.1210+41del	ADAMTS9	Deletion (intron variant)	not provided	GBenign
Select item 1271529	NM_182920.2(ADAMTS9):c.1210+36C>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227225	NM_182920.2(ADAMTS9):c.1210+16G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275113	NM_182920.2(ADAMTS9):c.1169+102G>C	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1236805	NM_182920.2(ADAMTS9):c.970-147G>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251343	NM_182920.2(ADAMTS9):c.792G>A (p.Glu264=)	ADAMTS9	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1250338	NM_182920.2(ADAMTS9):c.680-151C>T	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273033	NM_182920.2(ADAMTS9):c.517-20C>A	ADAMTS9	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277022	NM_182920.2(ADAMTS9):c.286T>A (p.Ser96Thr)	ADAMTS9, ADAMTS9-AS2 (S96T)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1263244	NM_182920.2(ADAMTS9):c.116-80C>G	ADAMTS9, ADAMTS9-AS2	Single nucleotide variant (intron variant)	not provided	GBenign

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 81