ClinVar Miner

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

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Total variants: 26
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HGVS dbSNP
NM_000363.5(TNNI3):c.108+59A>G rs143098258
NM_000363.5(TNNI3):c.109-20G>C rs1555864156
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.225T>G (p.Ala75=) rs1555864028
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712
NM_000363.5(TNNI3):c.24+19G>A rs368708903
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.264G>A (p.Leu88=) rs772928416
NM_000363.5(TNNI3):c.282+16_282+17delinsTT rs1555864004
NM_000363.5(TNNI3):c.282+6G>C rs1210217999
NM_000363.5(TNNI3):c.283-202G>T rs1005638211
NM_000363.5(TNNI3):c.283-221C>G rs140633085
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872
NM_000363.5(TNNI3):c.309T>C (p.Arg103=) rs749136271
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136
NM_000363.5(TNNI3):c.372+20C>T rs529338677
NM_000363.5(TNNI3):c.373-15C>T rs192630178
NM_000363.5(TNNI3):c.373-16C>T rs373508654
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457
NM_000363.5(TNNI3):c.549+267T>A rs11671448
NM_000363.5(TNNI3):c.550-157T>A rs114949974
NM_000363.5(TNNI3):c.594G>C (p.Leu198=) rs1599907577
NM_000363.5(TNNI3):c.618A>G (p.Lys206=) rs1374789557

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