List of variants in gene STIL reported as likely benign for not provided

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 98

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HGVS	dbSNP	gnomAD frequency
NM_001048166.1(STIL):c.873-59A>G	rs17103075	0.01721
NM_001048166.1(STIL):c.453+18C>T	rs75983191	0.01360
NM_001048166.1(STIL):c.2017A>G (p.Ser673Gly)	rs140448154	0.01146
NM_001048166.1(STIL):c.152+165C>T	rs61121898	0.01130
NM_001048166.1(STIL):c.1133+144C>G	rs141487071	0.00861
NM_001048166.1(STIL):c.454-288A>T	rs115521440	0.00858
NM_001048166.1(STIL):c.1024-225G>A	rs116403336	0.00857
NM_001048166.1(STIL):c.454-231G>T	rs149033908	0.00851
NM_001048166.1(STIL):c.153-217T>C	rs74935306	0.00680
NM_001048166.1(STIL):c.2830-54G>A	rs114760199	0.00629
NM_001048166.1(STIL):c.2383+257T>G	rs192733555	0.00588
NM_001048166.1(STIL):c.45-141_45-140insT	rs200202421	0.00558
NM_001048166.1(STIL):c.3378A>G (p.Arg1126=)	rs142315727	0.00478
NM_001048166.1(STIL):c.3786G>A (p.Thr1262=)	rs146387723	0.00460
NM_001048166.1(STIL):c.153-166C>T	rs144253309	0.00447
NM_001048166.1(STIL):c.2829+85G>A	rs149535653	0.00418
NM_001048166.1(STIL):c.701+147G>T	rs17097016	0.00402
NM_001048166.1(STIL):c.873-68C>T	rs140720630	0.00388
NM_001048166.1(STIL):c.2829+227G>A	rs116435567	0.00328
NM_001048166.1(STIL):c.1055G>A (p.Arg352His)	rs141678367	0.00323
NM_001048166.1(STIL):c.2829+116T>C	rs55740910	0.00313
NM_001048166.1(STIL):c.1136C>T (p.Ser379Phe)	rs149185431	0.00258
NM_001048166.1(STIL):c.3581C>T (p.Pro1194Leu)	rs144746030	0.00220
NM_001048166.1(STIL):c.1069G>A (p.Ala357Thr)	rs75426387	0.00194
NM_001048166.1(STIL):c.1455G>C (p.Leu485Phe)	rs139912214	0.00193
NM_001048166.1(STIL):c.2906A>G (p.His969Arg)	rs148193936	0.00085
NM_001048166.1(STIL):c.3156C>T (p.Ser1052=)	rs113337758	0.00043
NM_001048166.1(STIL):c.1005A>G (p.Glu335=)	rs149296029	0.00030
NM_001048166.1(STIL):c.152+4T>C	rs368201717	0.00029
NM_001048166.1(STIL):c.3276C>T (p.Asp1092=)	rs147478467	0.00028
NM_001048166.1(STIL):c.2064G>A (p.Pro688=)	rs138834578	0.00021
NM_001048166.1(STIL):c.1848G>A (p.Pro616=)	rs530746969	0.00020
NM_001048166.1(STIL):c.1146G>A (p.Lys382=)	rs564419897	0.00019
NM_001048166.1(STIL):c.3437C>T (p.Ala1146Val)	rs3766317	0.00007
NM_001048166.1(STIL):c.1179C>T (p.His393=)	rs200088144	0.00006
NM_001048166.1(STIL):c.1914A>G (p.Gln638=)	rs759881387	0.00006
NM_001048166.1(STIL):c.1227T>C (p.Ser409=)	rs200532713	0.00004
NM_001048166.1(STIL):c.1263A>G (p.Gln421=)	rs28705368	0.00004
NM_001048166.1(STIL):c.283T>C (p.Leu95=)	rs186741500	0.00004
NM_001048166.1(STIL):c.567T>C (p.His189=)	rs145024225	0.00003
NM_001048166.1(STIL):c.1172A>G (p.His391Arg)	rs545797279	0.00002
NM_001048166.1(STIL):c.3699C>T (p.Thr1233=)	rs763127279	0.00002
NM_001048166.1(STIL):c.453+10A>G	rs992978458	0.00002
NM_001048166.1(STIL):c.741G>A (p.Leu247=)	rs200629269	0.00002
NM_001048166.1(STIL):c.84A>G (p.Pro28=)	rs572125774	0.00002
NM_001048166.1(STIL):c.1053C>A (p.Ile351=)	rs1159321511	0.00001
NM_001048166.1(STIL):c.2880G>A (p.Pro960=)	rs774354721	0.00001
NM_001048166.1(STIL):c.3207T>C (p.Ala1069=)	rs778016364	0.00001
NM_001048166.1(STIL):c.454-10G>A	rs1045195933	0.00001
NM_001048166.1(STIL):c.882A>C (p.Ser294=)	rs1441619920	0.00001
NM_001048166.1(STIL):c.1023+16G>C
NM_001048166.1(STIL):c.1068C>T (p.Ser356=)
NM_001048166.1(STIL):c.1133+10C>G	rs539623822
NM_001048166.1(STIL):c.1143A>G (p.Gln381=)
NM_001048166.1(STIL):c.1170A>T (p.Ile390=)
NM_001048166.1(STIL):c.1182C>T (p.Asp394=)
NM_001048166.1(STIL):c.1203T>C (p.Asp401=)	rs2148989304
NM_001048166.1(STIL):c.1333T>C (p.Leu445=)
NM_001048166.1(STIL):c.1389G>A (p.Lys463=)
NM_001048166.1(STIL):c.1398A>G (p.Gln466=)	rs769152242
NM_001048166.1(STIL):c.1452C>A (p.Ser484=)
NM_001048166.1(STIL):c.1548C>T (p.Pro516=)	rs375423064
NM_001048166.1(STIL):c.1557G>A (p.Arg519=)
NM_001048166.1(STIL):c.186C>T (p.Ile62=)	rs1305828212
NM_001048166.1(STIL):c.1932C>T (p.His644=)
NM_001048166.1(STIL):c.1986T>C (p.Pro662=)
NM_001048166.1(STIL):c.2070A>C (p.Ser690=)	rs367887740
NM_001048166.1(STIL):c.2070A>T (p.Ser690=)	rs367887740
NM_001048166.1(STIL):c.2218-310G>A	rs114437803
NM_001048166.1(STIL):c.2259C>T (p.Ser753=)	rs774035449
NM_001048166.1(STIL):c.2286A>G (p.Thr762=)
NM_001048166.1(STIL):c.255A>G (p.Thr85=)
NM_001048166.1(STIL):c.2615+256dup	rs554696283
NM_001048166.1(STIL):c.2616-15A>G
NM_001048166.1(STIL):c.2616-246A>T	rs2821092
NM_001048166.1(STIL):c.261C>T (p.Asp87=)
NM_001048166.1(STIL):c.2766G>A (p.Glu922=)
NM_001048166.1(STIL):c.2793A>G (p.Gln931=)
NM_001048166.1(STIL):c.2830-19T>A	rs765585891
NM_001048166.1(STIL):c.2928C>T (p.Asn976=)
NM_001048166.1(STIL):c.2940A>G (p.Thr980=)
NM_001048166.1(STIL):c.3066C>T (p.Asn1022=)
NM_001048166.1(STIL):c.3080+9T>C
NM_001048166.1(STIL):c.3096C>T (p.Ile1032=)
NM_001048166.1(STIL):c.3240A>G (p.Gln1080=)
NM_001048166.1(STIL):c.3546T>C (p.Ser1182=)
NM_001048166.1(STIL):c.3579G>A (p.Thr1193=)	rs749339741
NM_001048166.1(STIL):c.3579G>T (p.Thr1193=)	rs749339741
NM_001048166.1(STIL):c.3582A>G (p.Pro1194=)
NM_001048166.1(STIL):c.3750T>A (p.Ile1250=)	rs1406402597
NM_001048166.1(STIL):c.453+230A>C	rs146950254
NM_001048166.1(STIL):c.624C>T (p.Pro208=)
NM_001048166.1(STIL):c.702-138_702-137del	rs140593303
NM_001048166.1(STIL):c.702-202G>T	rs77958283
NM_001048166.1(STIL):c.785+12A>G
NM_001048166.1(STIL):c.872+10A>G
NM_001048166.1(STIL):c.872+18C>T
NM_001048166.1(STIL):c.873-6G>A

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