ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance by Color Diagnostics, LLC DBA Color Health

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 94
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702 0.00006
NM_000363.5(TNNI3):c.236G>T (p.Arg79Leu) rs397516342 0.00004
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068 0.00004
NM_000363.5(TNNI3):c.293G>A (p.Arg98Gln) rs747522089 0.00004
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425 0.00004
NM_000363.5(TNNI3):c.373-11T>A rs746918706 0.00004
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512 0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571 0.00002
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu) rs777782551 0.00002
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445 0.00002
NM_000363.5(TNNI3):c.146dup (p.Lys50fs) rs1162696593 0.00001
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086 0.00001
NM_000363.5(TNNI3):c.152C>T (p.Thr51Ile) rs1366283106 0.00001
NM_000363.5(TNNI3):c.164A>C (p.Gln55Pro) rs775512887 0.00001
NM_000363.5(TNNI3):c.217G>C (p.Gly73Arg) rs1170054667 0.00001
NM_000363.5(TNNI3):c.233C>T (p.Thr78Ile) rs786205288 0.00001
NM_000363.5(TNNI3):c.278T>C (p.Leu93Pro) rs776035548 0.00001
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344 0.00001
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn) rs766958196 0.00001
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088 0.00001
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser) rs553214254 0.00001
NM_000363.5(TNNI3):c.35C>T (p.Pro12Leu) rs768052584 0.00001
NM_000363.5(TNNI3):c.368C>T (p.Thr123Met) rs397516345 0.00001
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506 0.00001
NM_000363.5(TNNI3):c.416T>G (p.Phe139Cys) rs1462112345 0.00001
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071 0.00001
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348 0.00001
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305 0.00001
NM_000363.5(TNNI3):c.620A>G (p.Lys207Arg) rs367672692 0.00001
NM_000363.5(TNNI3):c.-13C>A rs2147286713
NM_000363.5(TNNI3):c.104C>T (p.Ala35Val) rs1190447904
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.114del (p.Lys38fs) rs772607683
NM_000363.5(TNNI3):c.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.116C>G (p.Ser39Cys) rs2085732731
NM_000363.5(TNNI3):c.122T>A (p.Ile41Asn) rs2085732683
NM_000363.5(TNNI3):c.136A>T (p.Lys46Ter) rs2085732554
NM_000363.5(TNNI3):c.15C>A (p.Ser5Arg) rs989588363
NM_000363.5(TNNI3):c.173A>C (p.Lys58Thr) rs878853955
NM_000363.5(TNNI3):c.175C>G (p.Gln59Glu) rs2085729446
NM_000363.5(TNNI3):c.179A>G (p.Glu60Gly) rs2085729410
NM_000363.5(TNNI3):c.194C>T (p.Ala65Val) rs1057518784
NM_000363.5(TNNI3):c.197A>G (p.Glu66Gly)
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.220C>A (p.Arg74Ser) rs375795196
NM_000363.5(TNNI3):c.220C>T (p.Arg74Cys) rs375795196
NM_000363.5(TNNI3):c.221_237dup (p.Cys80delinsAlaLeuTer) rs2085728611
NM_000363.5(TNNI3):c.223G>T (p.Ala75Ser) rs1187997222
NM_000363.5(TNNI3):c.227T>C (p.Leu76Pro) rs1443859469
NM_000363.5(TNNI3):c.235C>A (p.Arg79Ser) rs3729712
NM_000363.5(TNNI3):c.235_236insT (p.Arg79fs) rs2085728638
NM_000363.5(TNNI3):c.239G>A (p.Cys80Tyr)
NM_000363.5(TNNI3):c.241C>T (p.Gln81Ter) rs2147284889
NM_000363.5(TNNI3):c.245C>G (p.Pro82Arg) rs752503819
NM_000363.5(TNNI3):c.25-10_25-8del rs2147286052
NM_000363.5(TNNI3):c.258del (p.Leu88fs) rs727503507
NM_000363.5(TNNI3):c.259G>C (p.Gly87Arg) rs1276684253
NM_000363.5(TNNI3):c.260G>C (p.Gly87Ala) rs2085728343
NM_000363.5(TNNI3):c.271G>A (p.Ala91Thr) rs1568859108
NM_000363.5(TNNI3):c.274G>A (p.Glu92Lys) rs2085728215
NM_000363.5(TNNI3):c.283-10C>A rs1470947353
NM_000363.5(TNNI3):c.292C>G (p.Arg98Gly) rs730881068
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe) rs773216333
NM_000363.5(TNNI3):c.307C>A (p.Arg103Ser) rs397516344
NM_000363.5(TNNI3):c.30G>T (p.Arg10Ser) rs2085738998
NM_000363.5(TNNI3):c.318G>C (p.Lys106Asn) rs750350912
NM_000363.5(TNNI3):c.328G>A (p.Glu110Lys) rs2147283707
NM_000363.5(TNNI3):c.337G>T (p.Asp113Tyr)
NM_000363.5(TNNI3):c.346G>A (p.Ala116Thr) rs2085716374
NM_000363.5(TNNI3):c.362A>T (p.Asn121Ile) rs2085716252
NM_000363.5(TNNI3):c.371_372+4del rs2085716080
NM_000363.5(TNNI3):c.373-11T>C rs746918706
NM_000363.5(TNNI3):c.389A>G (p.Gln130Arg) rs1390435424
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly) rs730881071
NM_000363.5(TNNI3):c.458C>T (p.Ala153Val) rs730881073
NM_000363.5(TNNI3):c.48_64del (p.Ala17fs) rs2085738631
NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro) rs1391407750
NM_000363.5(TNNI3):c.52C>G (p.Pro18Ala) rs779416591
NM_000363.5(TNNI3):c.539A>G (p.Asp180Gly) rs1060499912
NM_000363.5(TNNI3):c.548A>G (p.Lys183Arg)
NM_000363.5(TNNI3):c.550-12G>T
NM_000363.5(TNNI3):c.55A>C (p.Ile19Leu) rs755862334
NM_000363.5(TNNI3):c.578A>G (p.Lys193Arg)
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.67TCC[1] (p.Ser24del) rs2085738445
NM_000363.5(TNNI3):c.71C>T (p.Ser24Phe) rs1056846497
NM_000363.5(TNNI3):c.73A>G (p.Asn25Asp) rs2085738407
NM_000363.5(TNNI3):c.74A>T (p.Asn25Ile) rs1555864368
NM_000363.5(TNNI3):c.75C>G (p.Asn25Lys) rs1568859781
NM_000363.5(TNNI3):c.82G>T (p.Ala28Ser)
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.91A>G (p.Thr31Ala) rs1298916040

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.