ClinVar Miner

List of variants in gene TNNI3 reported as likely benign for not specified

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Total variants: 34
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HGVS dbSNP
NM_000363.5(TNNI3):c.105C>A (p.Ala35=) rs397516339
NM_000363.5(TNNI3):c.109-20G>C rs1555864156
NM_000363.5(TNNI3):c.12-7del rs370714315
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941
NM_000363.5(TNNI3):c.150+13G>T rs73617692
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.244C>T (p.Pro82Ser) rs77615401
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343
NM_000363.5(TNNI3):c.25-4C>T rs202086705
NM_000363.5(TNNI3):c.258C>T (p.Ala86=) rs727503508
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.303C>T (p.His101=) rs199539066
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.336C>T (p.Tyr112=) rs559450042
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136
NM_000363.5(TNNI3):c.372+20C>T rs529338677
NM_000363.5(TNNI3):c.372+7C>T rs367809676
NM_000363.5(TNNI3):c.373-15C>G rs192630178
NM_000363.5(TNNI3):c.373-15C>T rs192630178
NM_000363.5(TNNI3):c.373-16C>T rs373508654
NM_000363.5(TNNI3):c.373-4C>G rs2288530
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346
NM_000363.5(TNNI3):c.417T>C (p.Phe139=) rs1371643118
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.550-10C>T rs201240150
NM_000363.5(TNNI3):c.6G>A (p.Ala2=) rs397516361

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