ClinVar Miner

List of variants in gene TNNI3 reported by Color Health, Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 139
Download table as spreadsheet
HGVS dbSNP
NM_000363.5(TNNI3):c.*3C>T rs1568856984
NM_000363.5(TNNI3):c.-13C>A
NM_000363.5(TNNI3):c.-8G>A
NM_000363.5(TNNI3):c.104C>T (p.Ala35Val) rs1190447904
NM_000363.5(TNNI3):c.109-15A>G rs779144176
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.116C>G (p.Ser39Cys)
NM_000363.5(TNNI3):c.12-4C>T
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.120G>A (p.Lys40=)
NM_000363.5(TNNI3):c.122T>A (p.Ile41Asn)
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.136A>T (p.Lys46Ter)
NM_000363.5(TNNI3):c.139T>C (p.Leu47=) rs587780967
NM_000363.5(TNNI3):c.146dup (p.Lys50fs)
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.151-12A>C
NM_000363.5(TNNI3):c.151-6C>G rs377258542
NM_000363.5(TNNI3):c.152C>T (p.Thr51Ile)
NM_000363.5(TNNI3):c.156G>A (p.Leu52=)
NM_000363.5(TNNI3):c.157C>T (p.Leu53=) rs763981651
NM_000363.5(TNNI3):c.15C>A (p.Ser5Arg)
NM_000363.5(TNNI3):c.164A>C (p.Gln55Pro) rs775512887
NM_000363.5(TNNI3):c.173A>C (p.Lys58Thr)
NM_000363.5(TNNI3):c.175C>G (p.Gln59Glu)
NM_000363.5(TNNI3):c.179A>G (p.Glu60Gly)
NM_000363.5(TNNI3):c.194C>T (p.Ala65Val) rs1057518784
NM_000363.5(TNNI3):c.198G>A (p.Glu66=) rs3729710
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.207C>G (p.Arg69=) rs201422579
NM_000363.5(TNNI3):c.217G>C (p.Gly73Arg)
NM_000363.5(TNNI3):c.220C>A (p.Arg74Ser)
NM_000363.5(TNNI3):c.220C>T (p.Arg74Cys)
NM_000363.5(TNNI3):c.221_237dup (p.Cys80delinsAlaLeuTer)
NM_000363.5(TNNI3):c.226C>T (p.Leu76=)
NM_000363.5(TNNI3):c.227T>C (p.Leu76Pro)
NM_000363.5(TNNI3):c.235C>A (p.Arg79Ser)
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712
NM_000363.5(TNNI3):c.235_236insT (p.Arg79fs)
NM_000363.5(TNNI3):c.24+6A>G
NM_000363.5(TNNI3):c.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.245C>G (p.Pro82Arg)
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.25-10_25-8del
NM_000363.5(TNNI3):c.25-4C>T rs202086705
NM_000363.5(TNNI3):c.259G>C (p.Gly87Arg)
NM_000363.5(TNNI3):c.260G>C (p.Gly87Ala)
NM_000363.5(TNNI3):c.271G>A (p.Ala91Thr)
NM_000363.5(TNNI3):c.273G>A (p.Ala91=) rs75491697
NM_000363.5(TNNI3):c.274G>A (p.Glu92Lys)
NM_000363.5(TNNI3):c.277C>T (p.Leu93=)
NM_000363.5(TNNI3):c.278T>C (p.Leu93Pro) rs776035548
NM_000363.5(TNNI3):c.279G>A (p.Leu93=) rs1568859087
NM_000363.5(TNNI3):c.283-10C>A
NM_000363.5(TNNI3):c.283-13G>T
NM_000363.5(TNNI3):c.283-9C>T rs759922995
NM_000363.5(TNNI3):c.28A>G (p.Arg10Gly)
NM_000363.5(TNNI3):c.292C>T (p.Arg98Ter) rs730881068
NM_000363.5(TNNI3):c.293G>A (p.Arg98Gln) rs747522089
NM_000363.5(TNNI3):c.294A>G (p.Arg98=) rs1568858567
NM_000363.5(TNNI3):c.298C>T (p.Leu100Phe) rs773216333
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872
NM_000363.5(TNNI3):c.307C>A (p.Arg103Ser)
NM_000363.5(TNNI3):c.307C>T (p.Arg103Cys) rs397516344
NM_000363.5(TNNI3):c.308G>A (p.Arg103His) rs371000425
NM_000363.5(TNNI3):c.30G>T (p.Arg10Ser)
NM_000363.5(TNNI3):c.318G>A (p.Lys106=) rs750350912
NM_000363.5(TNNI3):c.318G>C (p.Lys106Asn)
NM_000363.5(TNNI3):c.322G>A (p.Asp108Asn)
NM_000363.5(TNNI3):c.328G>A (p.Glu110Lys)
NM_000363.5(TNNI3):c.330G>A (p.Glu110=)
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088
NM_000363.5(TNNI3):c.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070
NM_000363.5(TNNI3):c.346G>A (p.Ala116Thr)
NM_000363.5(TNNI3):c.347C>G (p.Ala116Gly) rs777177571
NM_000363.5(TNNI3):c.34C>T (p.Pro12Ser)
NM_000363.5(TNNI3):c.354C>T (p.Val118=)
NM_000363.5(TNNI3):c.356C>A (p.Thr119Asn) rs184709702
NM_000363.5(TNNI3):c.35C>T (p.Pro12Leu)
NM_000363.5(TNNI3):c.362A>T (p.Asn121Ile)
NM_000363.5(TNNI3):c.368C>T (p.Thr123Met) rs397516345
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.371_372+4del
NM_000363.5(TNNI3):c.373-11T>A
NM_000363.5(TNNI3):c.373-11T>C
NM_000363.5(TNNI3):c.373-14del
NM_000363.5(TNNI3):c.373-15C>G rs192630178
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.373-8G>A rs369244036
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.389A>G (p.Gln130Arg) rs1390435424
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346
NM_000363.5(TNNI3):c.402C>T (p.Asp134=)
NM_000363.5(TNNI3):c.416T>G (p.Phe139Cys)
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly)
NM_000363.5(TNNI3):c.422G>A (p.Arg141Gln) rs397516347
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.432G>C (p.Leu144=)
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.434G>A (p.Arg145Gln) rs397516349
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu)
NM_000363.5(TNNI3):c.458C>T (p.Ala153Val)
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305
NM_000363.5(TNNI3):c.484C>T (p.Arg162Trp) rs368861241
NM_000363.5(TNNI3):c.485G>A (p.Arg162Gln) rs397516354
NM_000363.5(TNNI3):c.48_64del (p.Ala17fs)
NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro)
NM_000363.5(TNNI3):c.508C>A (p.Arg170=)
NM_000363.5(TNNI3):c.516C>T (p.His172=)
NM_000363.5(TNNI3):c.522G>A (p.Lys174=)
NM_000363.5(TNNI3):c.52C>G (p.Pro18Ala)
NM_000363.5(TNNI3):c.550-10C>T rs201240150
NM_000363.5(TNNI3):c.550-12G>A
NM_000363.5(TNNI3):c.550-13C>T
NM_000363.5(TNNI3):c.550-14T>C
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512
NM_000363.5(TNNI3):c.55A>G (p.Ile19Val) rs755862334
NM_000363.5(TNNI3):c.567A>G (p.Gly189=) rs902161211
NM_000363.5(TNNI3):c.581A>C (p.Asn194Thr) rs730881081
NM_000363.5(TNNI3):c.585C>T (p.Ile195=)
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn) rs104894727
NM_000363.5(TNNI3):c.5C>T (p.Ala2Val) rs397516359
NM_000363.5(TNNI3):c.606G>A (p.Glu202=) rs796474405
NM_000363.5(TNNI3):c.612C>G (p.Arg204=)
NM_000363.5(TNNI3):c.67TCC[1] (p.Ser24del)
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361
NM_000363.5(TNNI3):c.71C>T (p.Ser24Phe)
NM_000363.5(TNNI3):c.73A>G (p.Asn25Asp)
NM_000363.5(TNNI3):c.74A>T (p.Asn25Ile)
NM_000363.5(TNNI3):c.75C>G (p.Asn25Lys) rs1568859781
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366
NM_000363.5(TNNI3):c.91A>G (p.Thr31Ala)
NM_000363.5(TNNI3):c.92C>T (p.Thr31Met) rs201928445
NM_000363.5(TNNI3):c.9T>C (p.Asp3=)

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.