ClinVar Miner

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

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Gene type:
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Total variants: 76
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HGVS dbSNP
NM_000363.5(TNNI3):c.-13C>A
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.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.116C>G (p.Ser39Cys)
NM_000363.5(TNNI3):c.122T>A (p.Ile41Asn)
NM_000363.5(TNNI3):c.136A>T (p.Lys46Ter)
NM_000363.5(TNNI3):c.146dup (p.Lys50fs)
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.152C>T (p.Thr51Ile)
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.204del (p.Arg69fs) rs727504872
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.227T>C (p.Leu76Pro)
NM_000363.5(TNNI3):c.235C>A (p.Arg79Ser)
NM_000363.5(TNNI3):c.235_236insT (p.Arg79fs)
NM_000363.5(TNNI3):c.245C>G (p.Pro82Arg)
NM_000363.5(TNNI3):c.25-10_25-8del
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.274G>A (p.Glu92Lys)
NM_000363.5(TNNI3):c.278T>C (p.Leu93Pro) rs776035548
NM_000363.5(TNNI3):c.283-10C>A
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.298C>T (p.Leu100Phe) rs773216333
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>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.331A>G (p.Arg111Gly) rs730881088
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.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.389A>G (p.Gln130Arg) rs1390435424
NM_000363.5(TNNI3):c.416T>G (p.Phe139Cys)
NM_000363.5(TNNI3):c.421C>G (p.Arg141Gly)
NM_000363.5(TNNI3):c.428C>A (p.Thr143Asn) rs397516348
NM_000363.5(TNNI3):c.439G>C (p.Val147Leu)
NM_000363.5(TNNI3):c.458C>T (p.Ala153Val)
NM_000363.5(TNNI3):c.482C>T (p.Ala161Val) rs753413305
NM_000363.5(TNNI3):c.48_64del (p.Ala17fs)
NM_000363.5(TNNI3):c.500T>C (p.Leu167Pro)
NM_000363.5(TNNI3):c.52C>G (p.Pro18Ala)
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512
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)
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

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