ClinVar Miner

List of variants in gene FPGT-TNNI3K, TNNI3K studied for atrial conduction disease

Included ClinVar conditions (1):
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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_015978.3(TNNI3K):c.1027+33T>G rs6424586 0.92549
NM_015978.3(TNNI3K):c.2431+30A>G rs3895907 0.42662
NM_015978.3(TNNI3K):c.1825+13A>C rs45589143 0.09225
NM_015978.3(TNNI3K):c.1773-20_1773-19insC rs200033057 0.02220
NM_015978.3(TNNI3K):c.2057T>C (p.Ile686Thr) rs3737564 0.00806
NM_015978.3(TNNI3K):c.334-8C>T rs45443204 0.00528
NM_015978.3(TNNI3K):c.969A>G (p.Lys323=) rs141955645 0.00136
NM_015978.3(TNNI3K):c.788C>T (p.Pro263Leu) rs34521608 0.00128
NM_015978.3(TNNI3K):c.1772G>C (p.Ser591Thr) rs145260115 0.00116
NM_015978.3(TNNI3K):c.2053C>T (p.Pro685Ser) rs143618297 0.00018
NM_015978.3(TNNI3K):c.193G>T (p.Glu65Ter) rs201061482 0.00008
NM_015978.3(TNNI3K):c.1471C>T (p.Arg491Cys) rs79936844 0.00004
NM_015978.3(TNNI3K):c.680A>T (p.Asp227Val) rs373725645 0.00004
NM_015978.3(TNNI3K):c.681T>C (p.Asp227=) rs757108060 0.00004
NM_015978.3(TNNI3K):c.1561G>A (p.Val521Ile) rs750338302 0.00002
NM_015978.3(TNNI3K):c.278G>A (p.Arg93His) rs749552940 0.00002
NM_015978.3(TNNI3K):c.1097T>C (p.Met366Thr) rs777378688 0.00001
NM_015978.3(TNNI3K):c.1153T>C (p.Cys385Arg) rs184306323 0.00001
NM_015978.3(TNNI3K):c.175A>G (p.Asn59Asp) rs780477698 0.00001
NM_015978.3(TNNI3K):c.1995C>A (p.Phe665Leu) rs776665374 0.00001
NM_015978.3(TNNI3K):c.2012C>T (p.Ala671Val) rs201064243 0.00001
NM_015978.3(TNNI3K):c.912C>G (p.Phe304Leu) rs763734400 0.00001
NM_015978.3(TNNI3K):c.1318A>C (p.Lys440Gln)
NM_015978.3(TNNI3K):c.1389T>G (p.Ile463Met)
NM_015978.3(TNNI3K):c.1392G>T (p.Glu464Asp)
NM_015978.3(TNNI3K):c.1577G>A (p.Gly526Asp) rs606231469
NM_015978.3(TNNI3K):c.1595C>T (p.Pro532Leu)
NM_015978.3(TNNI3K):c.1615A>G (p.Thr539Ala) rs1662479663
NM_015978.3(TNNI3K):c.1747C>T (p.Pro583Ser)
NM_015978.3(TNNI3K):c.1921C>T (p.Arg641Trp)
NM_015978.3(TNNI3K):c.290T>G (p.Leu97Arg)
NM_015978.3(TNNI3K):c.333+2T>C rs762721434
NM_015978.3(TNNI3K):c.368G>A (p.Ser123Asn)
NM_015978.3(TNNI3K):c.503del (p.Phe168fs) rs751624085
NM_015978.3(TNNI3K):c.530A>G (p.Tyr177Cys)
NM_015978.3(TNNI3K):c.538G>T (p.Glu180Ter)
NM_015978.3(TNNI3K):c.731G>T (p.Arg244Leu)

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