ClinVar Miner

List of variants in gene TNNI3 reported as likely pathogenic by GeneDx

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Gene type:
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Total variants: 19
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HGVS dbSNP
NM_000363.5(TNNI3):c.114A>T (p.Lys38Asn) rs730881066
NM_000363.5(TNNI3):c.131C>G (p.Ser44Trp) rs730881085
NM_000363.5(TNNI3):c.302A>G (p.His101Arg) rs730881087
NM_000363.5(TNNI3):c.421C>T (p.Arg141Trp) rs730881071
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.451G>A (p.Ala151Thr) rs730881072
NM_000363.5(TNNI3):c.493G>T (p.Glu165Ter) rs1057521530
NM_000363.5(TNNI3):c.502G>A (p.Asp168Asn) rs1085308019
NM_000363.5(TNNI3):c.514C>G (p.His172Asp) rs730881075
NM_000363.5(TNNI3):c.521A>C (p.Lys174Thr) rs730881076
NM_000363.5(TNNI3):c.554A>G (p.Asn185Ser) rs730881079
NM_000363.5(TNNI3):c.562G>A (p.Val188Met) rs193922409
NM_000363.5(TNNI3):c.579G>T (p.Lys193Asn) rs397516358
NM_000363.5(TNNI3):c.581A>G (p.Asn194Ser) rs730881081
NM_000363.5(TNNI3):c.582C>G (p.Asn194Lys) rs730881090
NM_000363.5(TNNI3):c.586G>A (p.Asp196Asn) rs104894727
NM_000363.5(TNNI3):c.592C>G (p.Leu198Val) rs727504285
NM_000363.5(TNNI3):c.596G>A (p.Ser199Asn) rs730881091

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