ClinVar Miner

List of variants in gene TNNI3 reported as uncertain significance by GeneDx

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Total variants: 27
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HGVS dbSNP
NM_000363.5(TNNI3):c.107A>C (p.Lys36Thr) rs886039441
NM_000363.5(TNNI3):c.108+2T>G rs1057520417
NM_000363.5(TNNI3):c.114dup (p.Ser39fs) rs772607683
NM_000363.5(TNNI3):c.150G>A (p.Lys50=) rs730881086
NM_000363.5(TNNI3):c.19G>C (p.Asp7His) rs1201960520
NM_000363.5(TNNI3):c.204del (p.Arg69fs) rs727504872
NM_000363.5(TNNI3):c.208G>A (p.Gly70Arg) rs730881067
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.308G>A (p.Arg103His) rs371000425
NM_000363.5(TNNI3):c.331A>G (p.Arg111Gly) rs730881088
NM_000363.5(TNNI3):c.340A>G (p.Ile114Val) rs730881070
NM_000363.5(TNNI3):c.356C>T (p.Thr119Ile) rs184709702
NM_000363.5(TNNI3):c.370G>C (p.Glu124Gln) rs727503506
NM_000363.5(TNNI3):c.406C>T (p.Arg136Ter) rs1393946566
NM_000363.5(TNNI3):c.407G>A (p.Arg136Gln) rs730881069
NM_000363.5(TNNI3):c.458C>A (p.Ala153Asp) rs730881073
NM_000363.5(TNNI3):c.463A>G (p.Met155Val) rs730881074
NM_000363.5(TNNI3):c.553A>T (p.Asn185Tyr) rs730881089
NM_000363.5(TNNI3):c.556C>T (p.Arg186Trp) rs760978512
NM_000363.5(TNNI3):c.562G>T (p.Val188Leu) rs193922409
NM_000363.5(TNNI3):c.570C>G (p.Asp190Glu) rs1131691856
NM_000363.5(TNNI3):c.577A>G (p.Lys193Glu) rs730881080
NM_000363.5(TNNI3):c.625G>A (p.Glu209Lys) rs727504268
NM_000363.5(TNNI3):c.626A>C (p.Glu209Ala) rs730881083
NM_000363.5(TNNI3):c.632G>T (p.Ter211Leu) rs730881084
NM_000363.5(TNNI3):c.88G>A (p.Ala30Thr) rs796104366

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