ClinVar Miner

List of variants studied for Atrial conduction disease by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_015978.3(TNNI3K):c.828-19A>C rs17095165 0.01740
NM_015978.3(TNNI3K):c.2181+20A>C rs142942027 0.00540
NM_015978.3(TNNI3K):c.334-8C>T rs45443204 0.00534
NM_015978.3(TNNI3K):c.512T>C (p.Leu171Ser) rs6685961 0.00169
NM_015978.3(TNNI3K):c.969A>G (p.Lys323=) rs141955645 0.00138
NM_015978.3(TNNI3K):c.1910C>T (p.Thr637Met) rs2274260 0.00122
NM_015978.3(TNNI3K):c.1772G>C (p.Ser591Thr) rs145260115 0.00116
NM_015978.3(TNNI3K):c.827+11T>C rs148757567 0.00102
NM_015978.3(TNNI3K):c.1878+10T>C rs199892485 0.00038
NM_015978.3(TNNI3K):c.1076T>G (p.Leu359Ter) rs142183632 0.00001
NM_015978.3(TNNI3K):c.1620A>G (p.Gln540=) rs55654209
NM_015978.3(TNNI3K):c.1709T>C (p.Val570Ala)
NM_015978.3(TNNI3K):c.720_721insGGGACTCCAT (p.Phe241fs) rs556027408
NM_015978.3(TNNI3K):c.908T>A (p.Ile303Asn) rs972201584
NM_015978.3(TNNI3K):c.929A>T (p.His310Leu) rs113229834

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