ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_000363.5(TNNI3):c.283-221C>G rs140633085 0.01308
NM_000363.5(TNNI3):c.108+59A>G rs143098258 0.01257
NM_000363.5(TNNI3):c.550-157T>A rs114949974 0.00877
NM_000363.4(TNNI3):c.-148A>G rs73935313 0.00695
NM_000363.5(TNNI3):c.109-170G>A rs189301935 0.00565
NC_000019.10:g.55151728G>T rs143032168 0.00555
NC_000019.10:g.55151712T>C rs142223367 0.00553
NM_000363.5(TNNI3):c.372+200C>G rs140862371 0.00386
NM_000363.5(TNNI3):c.373-43G>A rs183956525 0.00343
NM_000363.5(TNNI3):c.550-112T>C rs140242923 0.00338
NM_000363.5(TNNI3):c.283-202G>T rs1005638211 0.00236
NM_000363.5(TNNI3):c.549+267T>A rs11671448 0.00175
NM_000363.5(TNNI3):c.235C>T (p.Arg79Cys) rs3729712 0.00048
NM_000363.5(TNNI3):c.373-16C>T rs373508654 0.00021
NM_000363.5(TNNI3):c.132G>C (p.Ser44=) rs727504941 0.00012
NM_000363.5(TNNI3):c.246G>T (p.Pro82=) rs397516343 0.00007
NM_000363.5(TNNI3):c.373-4C>G rs2288530 0.00007
NM_000363.5(TNNI3):c.363C>T (p.Asn121=) rs371490136 0.00006
NM_000363.5(TNNI3):c.39C>G (p.Arg13=) rs397516346 0.00005
NM_000363.5(TNNI3):c.303C>T (p.His101=) rs199539066 0.00004
NM_000363.5(TNNI3):c.304G>A (p.Ala102Thr) rs374618872 0.00003
NM_000363.5(TNNI3):c.471G>A (p.Ala157=) rs747756509 0.00002
NM_000363.5(TNNI3):c.24+19G>A rs368708903 0.00001
NM_000363.5(TNNI3):c.282+6G>C rs1210217999 0.00001
NM_000363.5(TNNI3):c.372+20C>T rs529338677 0.00001
NM_000363.5(TNNI3):c.384G>A (p.Leu128=) rs373130533 0.00001
NM_000363.5(TNNI3):c.474G>C (p.Leu158=) rs749880457 0.00001
NM_000363.5(TNNI3):c.109-20G>C rs1555864156
NM_000363.5(TNNI3):c.225T>G (p.Ala75=) rs1555864028
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.309T>C (p.Arg103=) rs749136271
NM_000363.5(TNNI3):c.373-15C>T rs192630178
NM_000363.5(TNNI3):c.432G>T (p.Leu144=) rs776615304
NM_000363.5(TNNI3):c.550-106_550-105insAGAC rs542316818
NM_000363.5(TNNI3):c.594G>C (p.Leu198=) rs1599907577
NM_000363.5(TNNI3):c.618A>G (p.Lys206=) rs1374789557

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