ClinVar Miner

List of variants in gene STIM1 reported as likely benign for hematologic disorder

Included ClinVar conditions (819):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 211
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001382567.1(STIM1):c.387A>G (p.Val129=) rs116855870 0.00083
NM_001382567.1(STIM1):c.114C>G (p.Ala38=) rs150033189 0.00029
NM_001382567.1(STIM1):c.386-11T>C rs368922449 0.00028
NM_001382567.1(STIM1):c.1128C>T (p.Ala376=) rs200375470 0.00020
NM_001382567.1(STIM1):c.140-15G>C rs202069849 0.00015
NM_001382567.1(STIM1):c.1568-9T>C rs201450136 0.00015
NM_001382567.1(STIM1):c.969+10T>G rs764751709 0.00015
NM_001382567.1(STIM1):c.570G>T (p.Leu190=) rs200233698 0.00013
NM_001382567.1(STIM1):c.105C>T (p.Ser35=) rs139540641 0.00012
NM_001382567.1(STIM1):c.792-8C>T rs201395930 0.00012
NM_001382567.1(STIM1):c.1634+11G>A rs199732479 0.00011
NM_001382567.1(STIM1):c.970-15C>G rs188804715 0.00011
NM_001382567.1(STIM1):c.1635-15C>T rs749764733 0.00009
NM_001382567.1(STIM1):c.408G>C (p.Glu136Asp) rs200648767 0.00009
NM_001382567.1(STIM1):c.774G>T (p.Leu258=) rs140997213 0.00009
NM_001382567.1(STIM1):c.603G>A (p.Gly201=) rs142843376 0.00008
NM_001382567.1(STIM1):c.975G>C (p.Arg325=) rs200963440 0.00008
NM_001382567.1(STIM1):c.139+6G>A rs200233935 0.00006
NM_001382567.1(STIM1):c.1474+16dup rs750124776 0.00006
NM_001382567.1(STIM1):c.872A>G (p.Asn291Ser) rs138848040 0.00005
NM_001382567.1(STIM1):c.1425C>T (p.Asp475=) rs200776986 0.00004
NM_001382567.1(STIM1):c.177G>A (p.Glu59=) rs553909431 0.00004
NM_001382567.1(STIM1):c.385+16G>A rs766833809 0.00004
NM_001382567.1(STIM1):c.108G>A (p.Ser36=) rs551284324 0.00003
NM_001382567.1(STIM1):c.1204C>T (p.Leu402=) rs201091587 0.00003
NM_001382567.1(STIM1):c.1251C>T (p.Ser417=) rs199782037 0.00003
NM_001382567.1(STIM1):c.1634+7A>G rs371193534 0.00003
NM_001382567.1(STIM1):c.271-19G>A rs763590946 0.00003
NM_001382567.1(STIM1):c.306A>G (p.Thr102=) rs140167452 0.00003
NM_001382567.1(STIM1):c.393T>C (p.Asn131=) rs764275626 0.00003
NM_001382567.1(STIM1):c.810G>A (p.Glu270=) rs201765594 0.00003
NM_001382567.1(STIM1):c.1068G>A (p.Glu356=) rs761203064 0.00002
NM_001382567.1(STIM1):c.1238+9C>T rs375604403 0.00002
NM_001382567.1(STIM1):c.1599C>T (p.Arg533=) rs377102721 0.00002
NM_001382567.1(STIM1):c.1656G>A (p.Ser552=) rs148209416 0.00002
NM_001382567.1(STIM1):c.1773C>T (p.Ile591=) rs1308455316 0.00002
NM_001382567.1(STIM1):c.270+13A>G rs201780058 0.00002
NM_001382567.1(STIM1):c.285C>T (p.Asp95=) rs780488492 0.00002
NM_001382567.1(STIM1):c.738G>A (p.Lys246=) rs536528954 0.00002
NM_001382567.1(STIM1):c.969+16A>G rs774941610 0.00002
NM_001382567.1(STIM1):c.1071G>A (p.Val357=) rs1288963987 0.00001
NM_001382567.1(STIM1):c.1089C>T (p.Asn363=) rs376193363 0.00001
NM_001382567.1(STIM1):c.1125G>T (p.Val375=) rs201975335 0.00001
NM_001382567.1(STIM1):c.1134G>A (p.Glu378=) rs920883663 0.00001
NM_001382567.1(STIM1):c.1185C>T (p.His395=) rs1027836784 0.00001
NM_001382567.1(STIM1):c.1238+10A>C rs201116081 0.00001
NM_001382567.1(STIM1):c.1239-10C>T rs201644728 0.00001
NM_001382567.1(STIM1):c.1299C>T (p.Ile433=) rs200738706 0.00001
NM_001382567.1(STIM1):c.1317C>T (p.Phe439=) rs1179975549 0.00001
NM_001382567.1(STIM1):c.139+16G>A rs754570282 0.00001
NM_001382567.1(STIM1):c.1623G>A (p.Leu541=) rs747948099 0.00001
NM_001382567.1(STIM1):c.1653T>C (p.Asp551=) rs1304754642 0.00001
NM_001382567.1(STIM1):c.1719T>A (p.Arg573=) rs200164426 0.00001
NM_001382567.1(STIM1):c.1725A>G (p.Ala575=) rs146393409 0.00001
NM_001382567.1(STIM1):c.1728C>T (p.Asp576=) rs542778043 0.00001
NM_001382567.1(STIM1):c.2142T>C (p.Leu714=) rs199935070 0.00001
NM_001382567.1(STIM1):c.228C>T (p.Asp76=) rs749540812 0.00001
NM_001382567.1(STIM1):c.300C>T (p.Asp100=) rs200658405 0.00001
NM_001382567.1(STIM1):c.348C>T (p.Ser116=) rs200075076 0.00001
NM_001382567.1(STIM1):c.385+7G>A rs370889167 0.00001
NM_001382567.1(STIM1):c.399C>T (p.Thr133=) rs199513192 0.00001
NM_001382567.1(STIM1):c.414A>G (p.Val138=) rs1319501573 0.00001
NM_001382567.1(STIM1):c.474G>A (p.Gln158=) rs1199018766 0.00001
NM_001382567.1(STIM1):c.498-4A>C rs977105613 0.00001
NM_001382567.1(STIM1):c.531T>A (p.Thr177=) rs767768485 0.00001
NM_001382567.1(STIM1):c.613+11T>A rs1048701700 0.00001
NM_001382567.1(STIM1):c.660C>T (p.Ile220=) rs200982503 0.00001
NM_001382567.1(STIM1):c.675C>T (p.Gly225=) rs151061361 0.00001
NM_001382567.1(STIM1):c.717G>A (p.Glu239=) rs1255140437 0.00001
NM_001382567.1(STIM1):c.744G>A (p.Leu248=) rs764311095 0.00001
NM_001382567.1(STIM1):c.909G>A (p.Leu303=) rs1402539076 0.00001
NM_001382567.1(STIM1):c.912G>C (p.Arg304=) rs533692595 0.00001
NM_001382567.1(STIM1):c.969+15A>T rs1457105275 0.00001
NM_001382567.1(STIM1):c.970-16C>A rs201003963 0.00001
NM_001382567.1(STIM1):c.1003C>T (p.Leu335=) rs202060449
NM_001382567.1(STIM1):c.108G>C (p.Ser36=) rs551284324
NM_001382567.1(STIM1):c.1119G>C (p.Leu373=)
NM_001382567.1(STIM1):c.1119G>T (p.Leu373=)
NM_001382567.1(STIM1):c.1122G>A (p.Leu374=)
NM_001382567.1(STIM1):c.1137+11C>G
NM_001382567.1(STIM1):c.1137+13C>T rs199507032
NM_001382567.1(STIM1):c.1137+14T>G
NM_001382567.1(STIM1):c.1137+18A>G
NM_001382567.1(STIM1):c.1138-11C>T rs2094472695
NM_001382567.1(STIM1):c.1138-14C>A
NM_001382567.1(STIM1):c.1138-15dup
NM_001382567.1(STIM1):c.1138-16G>A rs2133223879
NM_001382567.1(STIM1):c.1138-4G>A rs1229330873
NM_001382567.1(STIM1):c.1138-8C>T rs750360122
NM_001382567.1(STIM1):c.1203C>G (p.Ser401=) rs2133224307
NM_001382567.1(STIM1):c.1221T>C (p.His407=) rs2133224417
NM_001382567.1(STIM1):c.1230A>G (p.Leu410=) rs200232554
NM_001382567.1(STIM1):c.1239-10_1239-9del
NM_001382567.1(STIM1):c.1239-17C>G rs2094474498
NM_001382567.1(STIM1):c.1239-20T>A rs2133225683
NM_001382567.1(STIM1):c.1239-4del rs2133225817
NM_001382567.1(STIM1):c.1239-6C>T rs2133225807
NM_001382567.1(STIM1):c.1239-8G>A
NM_001382567.1(STIM1):c.1246C>T (p.Leu416=) rs1198313077
NM_001382567.1(STIM1):c.1272G>A (p.Arg424=) rs2133225953
NM_001382567.1(STIM1):c.129C>T (p.Ser43=)
NM_001382567.1(STIM1):c.1347A>C (p.Ser449=) rs765057580
NM_001382567.1(STIM1):c.139+13T>A rs2135171514
NM_001382567.1(STIM1):c.139+7C>A rs2090371877
NM_001382567.1(STIM1):c.140-16T>G
NM_001382567.1(STIM1):c.140-5C>T
NM_001382567.1(STIM1):c.140-9C>T
NM_001382567.1(STIM1):c.1428C>T (p.Asp476=) rs776633274
NM_001382567.1(STIM1):c.1461C>G (p.Pro487=) rs751169800
NM_001382567.1(STIM1):c.1461C>T (p.Pro487=) rs751169800
NM_001382567.1(STIM1):c.1474+17C>T
NM_001382567.1(STIM1):c.1474+17del
NM_001382567.1(STIM1):c.1474+20G>A
NM_001382567.1(STIM1):c.1568-10C>T
NM_001382567.1(STIM1):c.1568-12T>C rs2133240089
NM_001382567.1(STIM1):c.1568-13A>T
NM_001382567.1(STIM1):c.1568-7C>G rs1234433480
NM_001382567.1(STIM1):c.1581G>A (p.Gln527=)
NM_001382567.1(STIM1):c.1593G>A (p.Arg531=) rs765806444
NM_001382567.1(STIM1):c.1605G>A (p.Thr535=)
NM_001382567.1(STIM1):c.1620C>G (p.Gly540=)
NM_001382567.1(STIM1):c.1620C>T (p.Gly540=)
NM_001382567.1(STIM1):c.1634+13C>A
NM_001382567.1(STIM1):c.1635-20C>G
NM_001382567.1(STIM1):c.1650C>T (p.Ser550=)
NM_001382567.1(STIM1):c.1722T>C (p.Ala574=) rs1007050130
NM_001382567.1(STIM1):c.1737C>A (p.Leu579=) rs2133263867
NM_001382567.1(STIM1):c.1749T>G (p.Thr583=)
NM_001382567.1(STIM1):c.1767G>A (p.Arg589=)
NM_001382567.1(STIM1):c.1779G>A (p.Gly593=)
NM_001382567.1(STIM1):c.1779G>T (p.Gly593=)
NM_001382567.1(STIM1):c.1785C>T (p.His595=) rs1590703370
NM_001382567.1(STIM1):c.1791G>T (p.Gly597=)
NM_001382567.1(STIM1):c.1809G>A (p.Leu603=)
NM_001382567.1(STIM1):c.192C>T (p.Ser64=) rs200345567
NM_001382567.1(STIM1):c.195C>T (p.Phe65=)
NM_001382567.1(STIM1):c.2130T>C (p.Phe710=) rs1554972256
NM_001382567.1(STIM1):c.2142T>A (p.Leu714=) rs199935070
NM_001382567.1(STIM1):c.240T>C (p.Asn80=)
NM_001382567.1(STIM1):c.246T>C (p.Asp82=)
NM_001382567.1(STIM1):c.270+11C>T
NM_001382567.1(STIM1):c.270+12C>T
NM_001382567.1(STIM1):c.270+19C>T
NM_001382567.1(STIM1):c.271-11T>C
NM_001382567.1(STIM1):c.271-19G>C
NM_001382567.1(STIM1):c.271-3034_271-3023del
NM_001382567.1(STIM1):c.297T>C (p.His99=)
NM_001382567.1(STIM1):c.333G>A (p.Glu111=)
NM_001382567.1(STIM1):c.339G>A (p.Lys113=)
NM_001382567.1(STIM1):c.342C>T (p.Leu114=)
NM_001382567.1(STIM1):c.345C>T (p.Ile115=) rs770736310
NM_001382567.1(STIM1):c.354G>A (p.Glu118=)
NM_001382567.1(STIM1):c.360G>A (p.Leu120=)
NM_001382567.1(STIM1):c.375G>A (p.Lys125=)
NM_001382567.1(STIM1):c.381A>G (p.Ser127=)
NM_001382567.1(STIM1):c.385+20T>G rs2136019322
NM_001382567.1(STIM1):c.385+7G>T
NM_001382567.1(STIM1):c.386-17C>G
NM_001382567.1(STIM1):c.386-18G>T
NM_001382567.1(STIM1):c.408G>A (p.Glu136=) rs200648767
NM_001382567.1(STIM1):c.438G>A (p.Glu146=)
NM_001382567.1(STIM1):c.469C>T (p.Leu157=) rs1554968984
NM_001382567.1(STIM1):c.495A>C (p.Pro165=)
NM_001382567.1(STIM1):c.497+16G>A
NM_001382567.1(STIM1):c.497+17G>A rs200086415
NM_001382567.1(STIM1):c.497+17G>T
NM_001382567.1(STIM1):c.498-14C>G
NM_001382567.1(STIM1):c.498-15T>C
NM_001382567.1(STIM1):c.498-16C>G
NM_001382567.1(STIM1):c.498-18T>A
NM_001382567.1(STIM1):c.498-6C>T
NM_001382567.1(STIM1):c.513C>T (p.Asn171=) rs2133104522
NM_001382567.1(STIM1):c.516C>G (p.Thr172=) rs2133104553
NM_001382567.1(STIM1):c.519C>A (p.Thr173=) rs768915274
NM_001382567.1(STIM1):c.537G>A (p.Leu179=)
NM_001382567.1(STIM1):c.546A>C (p.Thr182=) rs2133104739
NM_001382567.1(STIM1):c.549C>T (p.Asp183=) rs1590681707
NM_001382567.1(STIM1):c.54C>T (p.His18=) rs2135170406
NM_001382567.1(STIM1):c.614-11CT[2]
NM_001382567.1(STIM1):c.614-20T>C
NM_001382567.1(STIM1):c.614-20T>G
NM_001382567.1(STIM1):c.614-4G>T rs2133161164
NM_001382567.1(STIM1):c.630C>T (p.His210=) rs199743104
NM_001382567.1(STIM1):c.660C>A (p.Ile220=) rs200982503
NM_001382567.1(STIM1):c.693T>C (p.Tyr231=)
NM_001382567.1(STIM1):c.699G>A (p.Gln233=)
NM_001382567.1(STIM1):c.69C>T (p.Leu23=) rs779453226
NM_001382567.1(STIM1):c.702C>T (p.Asn234=)
NM_001382567.1(STIM1):c.729G>A (p.Lys243=)
NM_001382567.1(STIM1):c.750G>T (p.Gly250=)
NM_001382567.1(STIM1):c.791+15T>G
NM_001382567.1(STIM1):c.792-3dup rs764247879
NM_001382567.1(STIM1):c.792-4C>A rs200996329
NM_001382567.1(STIM1):c.792-4C>G rs200996329
NM_001382567.1(STIM1):c.792-4C>T rs200996329
NM_001382567.1(STIM1):c.792-8C>A rs201395930
NM_001382567.1(STIM1):c.792-9C>A rs200264068
NM_001382567.1(STIM1):c.792-9C>T
NM_001382567.1(STIM1):c.801G>A (p.Lys267=)
NM_001382567.1(STIM1):c.831G>T (p.Val277=)
NM_001382567.1(STIM1):c.840C>G (p.Val280=) rs2133185849
NM_001382567.1(STIM1):c.843T>C (p.His281=) rs760049621
NM_001382567.1(STIM1):c.846G>C (p.Leu282=)
NM_001382567.1(STIM1):c.870C>T (p.Ile290=)
NM_001382567.1(STIM1):c.921T>C (p.Thr307=) rs2133186424
NM_001382567.1(STIM1):c.954G>A (p.Glu318=)
NM_001382567.1(STIM1):c.969+7G>T
NM_001382567.1(STIM1):c.969+9G>A
NM_001382567.1(STIM1):c.970-19C>T
NM_001382567.1(STIM1):c.970-6G>T
NM_001382567.1(STIM1):c.982T>C (p.Leu328=) rs2133220776

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.