ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
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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