Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
19 | g.55151840C>A | CA407439391 | TNNI3 | c.627G>T (p.Glu209Asp) c.660G>T (p.Glu220Asp) n.626G>T c.552G>T (p.Glu184Asp) n.455G>T | |
19 | g.55151840C= | CA2343272431 | TNNI3 | c.627G= (p.Glu209=) c.660G= (p.Glu220=) n.626G= c.552G= (p.Glu184=) n.455G= | |
19 | g.55151840C>G | CA407439393 | TNNI3 | c.627G>C (p.Glu209Asp) c.660G>C (p.Glu220Asp) n.626G>C c.552G>C (p.Glu184Asp) n.455G>C | ClinVar dbSNP |
19 | g.55151840C>T | CA508989325 | TNNI3 | c.627G>A (p.Glu209=) c.660G>A (p.Glu220=) n.626G>A c.552G>A (p.Glu184=) n.455G>A | gnomAD v4 |
19 | g.55151841T>A | CA407439397 | TNNI3 | c.626A>T (p.Glu209Val) c.659A>T (p.Glu220Val) n.625A>T c.551A>T (p.Glu184Val) n.454A>T | |
19 | g.55151841T>C | CA407439399 | TNNI3 | c.626A>G (p.Glu209Gly) c.659A>G (p.Glu220Gly) n.625A>G c.551A>G (p.Glu184Gly) n.454A>G | dbSNP gnomAD v2 gnomAD v4 |
19 | g.55151841T>G | CA022103 | TNNI3 | c.626A>C (p.Glu209Ala) c.659A>C (p.Glu220Ala) n.625A>C c.551A>C (p.Glu184Ala) n.454A>C | ClinVar dbSNP |
19 | g.55151841T= | CA2343272433 | TNNI3 | c.626A= (p.Glu209=) c.659A= (p.Glu220=) n.625A= c.551A= (p.Glu184=) n.454A= | |
19 | g.55151842C>A | CA407439402 | TNNI3 | c.625G>T (p.Glu209Ter) c.658G>T (p.Glu220Ter) n.624G>T c.550G>T (p.Glu184Ter) n.453G>T | gnomAD v4 |
19 | g.55151842C= | CA2343272437 | TNNI3 | c.625G= (p.Glu209=) c.658G= (p.Glu220=) n.624G= c.550G= (p.Glu184=) n.453G= | |
19 | g.55151842C>G | CA407439405 | TNNI3 | c.625G>C (p.Glu209Gln) c.658G>C (p.Glu220Gln) n.624G>C c.550G>C (p.Glu184Gln) n.453G>C | |
19 | g.55151842C>T | CA022097 | TNNI3 | c.625G>A (p.Glu209Lys) c.658G>A (p.Glu220Lys) n.624G>A c.550G>A (p.Glu184Lys) n.453G>A | ClinVar dbSNP COSMIC |
19 | g.55151843A= | CA2343272443 | TNNI3 | c.624T= (p.Phe208=) c.657T= (p.Phe219=) n.623T= c.549T= (p.Phe183=) n.452T= | |
19 | g.55151843A>C | CA10577112 | TNNI3 | c.624T>G (p.Phe208Leu) c.657T>G (p.Phe219Leu) n.623T>G c.549T>G (p.Phe183Leu) n.452T>G | ClinVar dbSNP |
19 | g.55151843A>G | CA508989326 | TNNI3 | c.624T>C (p.Phe208=) c.657T>C (p.Phe219=) n.623T>C c.549T>C (p.Phe183=) n.452T>C | |
19 | g.55151843A>T | CA407439408 | TNNI3 | c.624T>A (p.Phe208Leu) c.657T>A (p.Phe219Leu) n.623T>A c.549T>A (p.Phe183Leu) n.452T>A | |
19 | g.55151845dup | CA915953048 | TNNI3 | c.624dup (p.Glu209Ter) c.657dup (p.Glu220Ter) n.623dup c.549dup (p.Glu184Ter) n.452dup | ClinVar dbSNP |
19 | g.55151844A>C | CA407439411 | TNNI3 | c.623T>G (p.Phe208Cys) c.656T>G (p.Phe219Cys) n.622T>G c.548T>G (p.Phe183Cys) n.451T>G | |
19 | g.55151844A>G | CA407439414 | TNNI3 | c.623T>C (p.Phe208Ser) c.656T>C (p.Phe219Ser) n.622T>C c.548T>C (p.Phe183Ser) n.451T>C | |
19 | g.55151844A>T | CA407439416 | TNNI3 | c.623T>A (p.Phe208Tyr) c.656T>A (p.Phe219Tyr) n.622T>A c.548T>A (p.Phe183Tyr) n.451T>A | |
19 | g.55151845A= | CA2343272444 | TNNI3 | c.622T= (p.Phe208=) c.655T= (p.Phe219=) n.621T= c.547T= (p.Phe183=) n.450T= | |
19 | g.55151845A>C | CA407439418 | TNNI3 | c.622T>G (p.Phe208Val) c.655T>G (p.Phe219Val) n.621T>G c.547T>G (p.Phe183Val) n.450T>G | |
19 | g.55151845A>G | CA407439420 | TNNI3 | c.622T>C (p.Phe208Leu) c.655T>C (p.Phe219Leu) n.621T>C c.547T>C (p.Phe183Leu) n.450T>C | |
19 | g.55151845A>T | CA10577113 | TNNI3 | c.622T>A (p.Phe208Ile) c.655T>A (p.Phe219Ile) n.621T>A c.547T>A (p.Phe183Ile) n.450T>A | ClinVar dbSNP |
19 | g.55151846C>A | CA407439424 | TNNI3 | c.621G>T (p.Lys207Asn) c.654G>T (p.Lys218Asn) n.620G>T c.546G>T (p.Lys182Asn) n.449G>T | |
19 | g.55151846C= | CA2343272446 | TNNI3 | c.621G= (p.Lys207=) c.654G= (p.Lys218=) n.620G= c.546G= (p.Lys182=) n.449G= | |
19 | g.55151846C>G | CA407439426 | TNNI3 | c.621G>C (p.Lys207Asn) c.654G>C (p.Lys218Asn) n.620G>C c.546G>C (p.Lys182Asn) n.449G>C | ClinVar dbSNP |
19 | g.55151846C>T | CA508989327 | TNNI3 | c.621G>A (p.Lys207=) c.654G>A (p.Lys218=) n.620G>A c.546G>A (p.Lys182=) n.449G>A | gnomAD v4 |
19 | g.55151846_55151847delinsCT | CA2343272445 | TNNI3 | c.620_621delinsAG (p.Lys207=) c.653_654delinsAG (p.Lys218=) n.619_620delinsAG c.545_546delinsAG (p.Lys182=) n.448_449delinsAG | |
19 | g.55151847T>A | CA407439428 | TNNI3 | c.620A>T (p.Lys207Met) c.653A>T (p.Lys218Met) n.619A>T c.545A>T (p.Lys182Met) n.448A>T | |
19 | g.55151847T>C | CA310144831 | TNNI3 | c.620A>G (p.Lys207Arg) c.653A>G (p.Lys218Arg) n.619A>G c.545A>G (p.Lys182Arg) n.448A>G | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151847T>G | CA407439432 | TNNI3 | c.620A>C (p.Lys207Thr) c.653A>C (p.Lys218Thr) n.619A>C c.545A>C (p.Lys182Thr) n.448A>C | |
19 | g.55151847T= | CA2343272447 | TNNI3 | c.620A= (p.Lys207=) c.653A= (p.Lys218=) n.619A= c.545A= (p.Lys182=) n.448A= | |
19 | g.55151851del | CA920140594 | TNNI3 | c.620del (p.Lys207SerfsTer14) c.653del (p.Lys218SerfsTer14) n.619del c.545del (p.Lys182SerfsTer14) n.448del | dbSNP |
19 | g.55151850_55151851del | CA2695229153 | TNNI3 | c.619_620del (p.Lys207ValfsTer2) c.652_653del (p.Lys218ValfsTer2) n.618_619del c.544_545del (p.Lys182ValfsTer2) n.447_448del | |
19 | g.55151848T>A | CA407439439 | TNNI3 | c.619A>T (p.Lys207Ter) c.652A>T (p.Lys218Ter) n.618A>T c.544A>T (p.Lys182Ter) n.447A>T | |
19 | g.55151848T>C | CA407439437 | TNNI3 | c.619A>G (p.Lys207Glu) c.652A>G (p.Lys218Glu) n.618A>G c.544A>G (p.Lys182Glu) n.447A>G | |
19 | g.55151848T>G | CA407439436 | TNNI3 | c.619A>C (p.Lys207Gln) c.652A>C (p.Lys218Gln) n.618A>C c.544A>C (p.Lys182Gln) n.447A>C | |
19 | g.55151849T>A | CA407439440 | TNNI3 | c.618A>T (p.Lys206Asn) c.651A>T (p.Lys217Asn) n.617A>T c.543A>T (p.Lys181Asn) n.446A>T | |
19 | g.55151849T>C | CA508989328 | TNNI3 | c.618A>G (p.Lys206=) c.651A>G (p.Lys217=) n.617A>G c.543A>G (p.Lys181=) n.446A>G | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.55151849T>G | CA407439442 | TNNI3 | c.618A>C (p.Lys206Asn) c.651A>C (p.Lys217Asn) n.617A>C c.543A>C (p.Lys181Asn) n.446A>C | |
19 | g.55151849T= | CA2343272448 | TNNI3 | c.618A= (p.Lys206=) c.651A= (p.Lys217=) n.617A= c.543A= (p.Lys181=) n.446A= | |
19 | g.55151850T>A | CA022085 | TNNI3 | c.617A>T (p.Lys206Ile) c.650A>T (p.Lys217Ile) n.616A>T c.542A>T (p.Lys181Ile) n.445A>T | ClinVar dbSNP |
19 | g.55151850T>C | CA407439444 | TNNI3 | c.617A>G (p.Lys206Arg) c.650A>G (p.Lys217Arg) n.616A>G c.542A>G (p.Lys181Arg) n.445A>G | |
19 | g.55151850T>G | CA407439446 | TNNI3 | c.617A>C (p.Lys206Thr) c.650A>C (p.Lys217Thr) n.616A>C c.542A>C (p.Lys181Thr) n.445A>C | |
19 | g.55151850T= | CA2343272450 | TNNI3 | c.617A= (p.Lys206=) c.650A= (p.Lys217=) n.616A= c.542A= (p.Lys181=) n.445A= | |
19 | g.55151851T>A | CA407439447 | TNNI3 | c.616A>T (p.Lys206Ter) c.649A>T (p.Lys217Ter) n.615A>T c.541A>T (p.Lys181Ter) n.444A>T | |
19 | g.55151851T>C | CA022079 | TNNI3 | c.616A>G (p.Lys206Glu) c.649A>G (p.Lys217Glu) n.615A>G c.541A>G (p.Lys181Glu) n.444A>G | ClinVar dbSNP |
19 | g.55151851T>G | CA022072 | TNNI3 | c.616A>C (p.Lys206Gln) c.649A>C (p.Lys217Gln) n.615A>C c.541A>C (p.Lys181Gln) n.444A>C | ClinVar dbSNP |
19 | g.55151851T= | CA2343272459 | TNNI3 | c.616A= (p.Lys206=) c.649A= (p.Lys217=) n.615A= c.541A= (p.Lys181=) n.444A= | |
19 | g.55151852C>A | CA407439450 | TNNI3 | c.615G>T (p.Lys205Asn) c.648G>T (p.Lys216Asn) n.614G>T c.540G>T (p.Lys180Asn) n.443G>T | ClinVar |
19 | g.55151852C>G | CA407439451 | TNNI3 | c.615G>C (p.Lys205Asn) c.648G>C (p.Lys216Asn) n.614G>C c.540G>C (p.Lys180Asn) n.443G>C | |
19 | g.55151852C>T | CA508989329 | TNNI3 | c.615G>A (p.Lys205=) c.648G>A (p.Lys216=) n.614G>A c.540G>A (p.Lys180=) n.443G>A | |
19 | g.55151853T>A | CA407439452 | TNNI3 | c.614A>T (p.Lys205Met) c.647A>T (p.Lys216Met) n.613A>T c.539A>T (p.Lys180Met) n.442A>T | |
19 | g.55151853T>C | CA407439453 | TNNI3 | c.614A>G (p.Lys205Arg) c.647A>G (p.Lys216Arg) n.613A>G c.539A>G (p.Lys180Arg) n.442A>G | |
19 | g.55151853T>G | CA407439454 | TNNI3 | c.614A>C (p.Lys205Thr) c.647A>C (p.Lys216Thr) n.613A>C c.539A>C (p.Lys180Thr) n.442A>C | ClinVar dbSNP |
19 | g.55151853T= | CA2343272465 | TNNI3 | c.614A= (p.Lys205=) c.647A= (p.Lys216=) n.613A= c.539A= (p.Lys180=) n.442A= | |
19 | g.55151854T>A | CA407439456 | TNNI3 | c.613A>T (p.Lys205Ter) c.646A>T (p.Lys216Ter) n.612A>T c.538A>T (p.Lys180Ter) n.441A>T | |
19 | g.55151854T>C | CA407439457 | TNNI3 | c.613A>G (p.Lys205Glu) c.646A>G (p.Lys216Glu) n.612A>G c.538A>G (p.Lys180Glu) n.441A>G | |
19 | g.55151854T>G | CA022066 | TNNI3 | c.613A>C (p.Lys205Gln) c.646A>C (p.Lys216Gln) n.612A>C c.538A>C (p.Lys180Gln) n.441A>C | ClinVar dbSNP |
19 | g.55151854T= | CA2343272470 | TNNI3 | c.613A= (p.Lys205=) c.646A= (p.Lys216=) n.612A= c.538A= (p.Lys180=) n.441A= | |
19 | g.55151855G>A | CA508989332 | TNNI3 | c.612C>T (p.Arg204=) c.645C>T (p.Arg215=) n.611C>T c.537C>T (p.Arg179=) n.440C>T | |
19 | g.55151855G>C | CA508989330 | TNNI3 | c.612C>G (p.Arg204=) c.645C>G (p.Arg215=) n.611C>G c.537C>G (p.Arg179=) n.440C>G | ClinVar dbSNP gnomAD v4 |
19 | g.55151855G= | CA2343272476 | TNNI3 | c.612C= (p.Arg204=) c.645C= (p.Arg215=) n.611C= c.537C= (p.Arg179=) n.440C= | |
19 | g.55151855G>T | CA508989331 | TNNI3 | c.612C>A (p.Arg204=) c.645C>A (p.Arg215=) n.611C>A c.537C>A (p.Arg179=) n.440C>A | dbSNP |
19 | g.55151856C>A | CA051933 | TNNI3 | c.611G>T (p.Arg204Leu) c.644G>T (p.Arg215Leu) n.610G>T c.536G>T (p.Arg179Leu) n.439G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
19 | g.55151856C= | CA2343272484 | TNNI3 | c.611G= (p.Arg204=) c.644G= (p.Arg215=) n.610G= c.536G= (p.Arg179=) n.439G= | |
19 | g.55151856C>G | CA407439460 | TNNI3 | c.611G>C (p.Arg204Pro) c.644G>C (p.Arg215Pro) n.610G>C c.536G>C (p.Arg179Pro) n.439G>C | |
19 | g.55151856C>T | CA022060 | TNNI3 | c.611G>A (p.Arg204His) c.644G>A (p.Arg215His) n.610G>A c.536G>A (p.Arg179His) n.439G>A | ClinVar dbSNP gnomAD v4 |
19 | g.55151857G>A | CA022054 | TNNI3 | c.610C>T (p.Arg204Cys) c.643C>T (p.Arg215Cys) n.609C>T c.535C>T (p.Arg179Cys) n.438C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 COSMIC |
19 | g.55151857G>C | CA407439463 | TNNI3 | c.610C>G (p.Arg204Gly) c.643C>G (p.Arg215Gly) n.609C>G c.535C>G (p.Arg179Gly) n.438C>G | |
19 | g.55151857G= | CA2343272490 | TNNI3 | c.610C= (p.Arg204=) c.643C= (p.Arg215=) n.609C= c.535C= (p.Arg179=) n.438C= | |
19 | g.55151857G>T | CA407439464 | TNNI3 | c.610C>A (p.Arg204Ser) c.643C>A (p.Arg215Ser) n.609C>A c.535C>A (p.Arg179Ser) n.438C>A | ClinVar dbSNP |
19 | g.55151858G>A | CA022049 | TNNI3 | c.609C>T (p.Gly203=) c.642C>T (p.Gly214=) n.608C>T c.534C>T (p.Gly178=) n.437C>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151858G>C | CA508989334 | TNNI3 | c.609C>G (p.Gly203=) c.642C>G (p.Gly214=) n.608C>G c.534C>G (p.Gly178=) n.437C>G | |
19 | g.55151858G= | CA2343272501 | TNNI3 | c.609C= (p.Gly203=) c.642C= (p.Gly214=) n.608C= c.534C= (p.Gly178=) n.437C= | |
19 | g.55151858G>T | CA508989333 | TNNI3 | c.609C>A (p.Gly203=) c.642C>A (p.Gly214=) n.608C>A c.534C>A (p.Gly178=) n.437C>A | |
19 | g.55151859C>A | CA407439466 | TNNI3 | c.608G>T (p.Gly203Val) c.641G>T (p.Gly214Val) n.607G>T c.533G>T (p.Gly178Val) n.436G>T | |
19 | g.55151859C>G | CA407439467 | TNNI3 | c.608G>C (p.Gly203Ala) c.641G>C (p.Gly214Ala) n.607G>C c.533G>C (p.Gly178Ala) n.436G>C | |
19 | g.55151859C>T | CA407439469 | TNNI3 | c.608G>A (p.Gly203Asp) c.641G>A (p.Gly214Asp) n.607G>A c.533G>A (p.Gly178Asp) n.436G>A | ClinVar |
19 | g.55151860C>A | CA407439470 | TNNI3 | c.607G>T (p.Gly203Cys) c.640G>T (p.Gly214Cys) n.606G>T c.532G>T (p.Gly178Cys) n.435G>T | |
19 | g.55151860C= | CA2343272506 | TNNI3 | c.607G= (p.Gly203=) c.640G= (p.Gly214=) n.606G= c.532G= (p.Gly178=) n.435G= | |
19 | g.55151860C>G | CA407439472 | TNNI3 | c.607G>C (p.Gly203Arg) c.640G>C (p.Gly214Arg) n.606G>C c.532G>C (p.Gly178Arg) n.435G>C | |
19 | g.55151860C>T | CA022043 | TNNI3 | c.607G>A (p.Gly203Ser) c.640G>A (p.Gly214Ser) n.606G>A c.532G>A (p.Gly178Ser) n.435G>A | ClinVar dbSNP |
19 | g.55151861C>A | CA407439474 | TNNI3 | c.606G>T (p.Glu202Asp) c.639G>T (p.Glu213Asp) n.605G>T c.531G>T (p.Glu177Asp) n.434G>T | |
19 | g.55151861C= | CA2343272513 | TNNI3 | c.606G= (p.Glu202=) c.639G= (p.Glu213=) n.605G= c.531G= (p.Glu177=) n.434G= | |
19 | g.55151861C>G | CA407439477 | TNNI3 | c.606G>C (p.Glu202Asp) c.639G>C (p.Glu213Asp) n.605G>C c.531G>C (p.Glu177Asp) n.434G>C | |
19 | g.55151861C>T | CA310144864 | TNNI3 | c.606G>A (p.Glu202=) c.639G>A (p.Glu213=) n.605G>A c.531G>A (p.Glu177=) n.434G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151862T>A | CA407439479 | TNNI3 | c.605A>T (p.Glu202Val) c.638A>T (p.Glu213Val) n.604A>T c.530A>T (p.Glu177Val) n.433A>T | |
19 | g.55151862T>C | CA407439480 | TNNI3 | c.605A>G (p.Glu202Gly) c.638A>G (p.Glu213Gly) n.604A>G c.530A>G (p.Glu177Gly) n.433A>G | ClinVar gnomAD v4 |
19 | g.55151862T>G | CA407439482 | TNNI3 | c.605A>C (p.Glu202Ala) c.638A>C (p.Glu213Ala) n.604A>C c.530A>C (p.Glu177Ala) n.433A>C | gnomAD v4 |
19 | g.55151863C>A | CA407439484 | TNNI3 | c.604G>T (p.Glu202Ter) c.637G>T (p.Glu213Ter) n.603G>T c.529G>T (p.Glu177Ter) n.432G>T | gnomAD v4 |
19 | g.55151863C= | CA2343272516 | TNNI3 | c.604G= (p.Glu202=) c.637G= (p.Glu213=) n.603G= c.529G= (p.Glu177=) n.432G= | |
19 | g.55151863C>G | CA407439485 | TNNI3 | c.604G>C (p.Glu202Gln) c.637G>C (p.Glu213Gln) n.603G>C c.529G>C (p.Glu177Gln) n.432G>C | ClinVar dbSNP gnomAD v2 gnomAD v4 |
19 | g.55151863C>T | CA407439486 | TNNI3 | c.604G>A (p.Glu202Lys) c.637G>A (p.Glu213Lys) n.603G>A c.529G>A (p.Glu177Lys) n.432G>A | |
19 | g.55151864C>A | CA407439488 | TNNI3 | c.603G>T (p.Met201Ile) c.636G>T (p.Met212Ile) n.602G>T c.528G>T (p.Met176Ile) n.431G>T | |
19 | g.55151864C= | CA2343272519 | TNNI3 | c.603G= (p.Met201=) c.636G= (p.Met212=) n.602G= c.528G= (p.Met176=) n.431G= | |
19 | g.55151864C>G | CA051926 | TNNI3 | c.603G>C (p.Met201Ile) c.636G>C (p.Met212Ile) n.602G>C c.528G>C (p.Met176Ile) n.431G>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151864C>T | CA407439490 | TNNI3 | c.603G>A (p.Met201Ile) c.636G>A (p.Met212Ile) n.602G>A c.528G>A (p.Met176Ile) n.431G>A | gnomAD v4 |
19 | g.55151865A= | CA2343272522 | TNNI3 | c.602T= (p.Met201=) c.635T= (p.Met212=) n.601T= c.527T= (p.Met176=) n.430T= | |
19 | g.55151865A>C | CA407439494 | TNNI3 | c.602T>G (p.Met201Arg) c.635T>G (p.Met212Arg) n.601T>G c.527T>G (p.Met176Arg) n.430T>G | |
19 | g.55151865A>G | CA022037 | TNNI3 | c.602T>C (p.Met201Thr) c.635T>C (p.Met212Thr) n.601T>C c.527T>C (p.Met176Thr) n.430T>C | ClinVar dbSNP |
19 | g.55151865A>T | CA407439492 | TNNI3 | c.602T>A (p.Met201Lys) c.635T>A (p.Met212Lys) n.601T>A c.527T>A (p.Met176Lys) n.430T>A | |
19 | g.55151866T>A | CA407439495 | TNNI3 | c.601A>T (p.Met201Leu) c.634A>T (p.Met212Leu) n.600A>T c.526A>T (p.Met176Leu) n.429A>T | |
19 | g.55151866T>C | CA407439497 | TNNI3 | c.601A>G (p.Met201Val) c.634A>G (p.Met212Val) n.600A>G c.526A>G (p.Met176Val) n.429A>G | gnomAD v4 |
19 | g.55151866T>G | CA407439496 | TNNI3 | c.601A>C (p.Met201Leu) c.634A>C (p.Met212Leu) n.600A>C c.526A>C (p.Met176Leu) n.429A>C | |
19 | g.55151867T>A | CA508989337 | TNNI3 | c.600A>T (p.Gly200=) c.633A>T (p.Gly211=) n.599A>T c.525A>T (p.Gly175=) n.428A>T | |
19 | g.55151867T>C | CA508989335 | TNNI3 | c.600A>G (p.Gly200=) c.633A>G (p.Gly211=) n.599A>G c.525A>G (p.Gly175=) n.428A>G | |
19 | g.55151867T>G | CA508989336 | TNNI3 | c.600A>C (p.Gly200=) c.633A>C (p.Gly211=) n.599A>C c.525A>C (p.Gly175=) n.428A>C | |
19 | g.55151868C>A | CA16616444 | TNNI3 | c.599G>T (p.Gly200Val) c.632G>T (p.Gly211Val) n.598G>T c.524G>T (p.Gly175Val) n.427G>T | ClinVar dbSNP |
19 | g.55151868C= | CA2343272527 | TNNI3 | c.599G= (p.Gly200=) c.632G= (p.Gly211=) n.598G= c.524G= (p.Gly175=) n.427G= | |
19 | g.55151868C>G | CA407439498 | TNNI3 | c.599G>C (p.Gly200Ala) c.632G>C (p.Gly211Ala) n.598G>C c.524G>C (p.Gly175Ala) n.427G>C | |
19 | g.55151868C>T | CA10583862 | TNNI3 | c.599G>A (p.Gly200Glu) c.632G>A (p.Gly211Glu) n.598G>A c.524G>A (p.Gly175Glu) n.427G>A | ClinVar dbSNP |
19 | g.55151869C>A | CA407439500 | TNNI3 | c.598G>T (p.Gly200Ter) c.631G>T (p.Gly211Ter) n.597G>T c.523G>T (p.Gly175Ter) n.426G>T | |
19 | g.55151869C>G | CA407439501 | TNNI3 | c.598G>C (p.Gly200Arg) c.631G>C (p.Gly211Arg) n.597G>C c.523G>C (p.Gly175Arg) n.426G>C | |
19 | g.55151869C>T | CA407439502 | TNNI3 | c.598G>A (p.Gly200Arg) c.631G>A (p.Gly211Arg) n.597G>A c.523G>A (p.Gly175Arg) n.426G>A | |
19 | g.55151870del | CA2580097811 | TNNI3 | c.597del (p.Ser199ArgfsTer22) c.630del (p.Ser210ArgfsTer22) n.596del c.522del (p.Ser174ArgfsTer22) n.425del | ClinVar |
19 | g.55151870A= | CA2343272532 | TNNI3 | c.597T= (p.Ser199=) c.630T= (p.Ser210=) n.596T= c.522T= (p.Ser174=) n.425T= | |
19 | g.55151870A>C | CA407439503 | TNNI3 | c.597T>G (p.Ser199Arg) c.630T>G (p.Ser210Arg) n.596T>G c.522T>G (p.Ser174Arg) n.425T>G | |
19 | g.55151870A>G | CA508989338 | TNNI3 | c.597T>C (p.Ser199=) c.630T>C (p.Ser210=) n.596T>C c.522T>C (p.Ser174=) n.425T>C | dbSNP gnomAD v3 gnomAD v4 |
19 | g.55151870A>T | CA407439505 | TNNI3 | c.597T>A (p.Ser199Arg) c.630T>A (p.Ser210Arg) n.596T>A c.522T>A (p.Ser174Arg) n.425T>A | |
19 | g.55151871C>A | CA407439507 | TNNI3 | c.596G>T (p.Ser199Ile) c.629G>T (p.Ser210Ile) n.595G>T c.521G>T (p.Ser174Ile) n.424G>T | |
19 | g.55151871C= | CA2343272536 | TNNI3 | c.596G= (p.Ser199=) c.629G= (p.Ser210=) n.595G= c.521G= (p.Ser174=) n.424G= | |
19 | g.55151871C>G | CA407439509 | TNNI3 | c.596G>C (p.Ser199Thr) c.629G>C (p.Ser210Thr) n.595G>C c.521G>C (p.Ser174Thr) n.424G>C | |
19 | g.55151871C>T | CA022024 | TNNI3 | c.596G>A (p.Ser199Asn) c.629G>A (p.Ser210Asn) n.595G>A c.521G>A (p.Ser174Asn) n.424G>A | ClinVar dbSNP gnomAD v4 |
19 | g.55151872T>A | CA407439519 | TNNI3 | c.595A>T (p.Ser199Cys) c.628A>T (p.Ser210Cys) n.594A>T c.520A>T (p.Ser174Cys) n.423A>T | ClinVar dbSNP |
19 | g.55151872T>C | CA407439517 | TNNI3 | c.595A>G (p.Ser199Gly) c.628A>G (p.Ser210Gly) n.594A>G c.520A>G (p.Ser174Gly) n.423A>G | dbSNP |
19 | g.55151872T>G | CA407439514 | TNNI3 | c.595A>C (p.Ser199Arg) c.628A>C (p.Ser210Arg) n.594A>C c.520A>C (p.Ser174Arg) n.423A>C | |
19 | g.55151872T= | CA2343272541 | TNNI3 | c.595A= (p.Ser199=) c.628A= (p.Ser210=) n.594A= c.520A= (p.Ser174=) n.423A= | |
19 | g.55151873C>A | CA508989341 | TNNI3 | c.594G>T (p.Leu198=) c.627G>T (p.Leu209=) n.593G>T c.519G>T (p.Leu173=) n.422G>T | |
19 | g.55151873C= | CA2343272544 | TNNI3 | c.594G= (p.Leu198=) c.627G= (p.Leu209=) n.593G= c.519G= (p.Leu173=) n.422G= | |
19 | g.55151873C>G | CA508989339 | TNNI3 | c.594G>C (p.Leu198=) c.627G>C (p.Leu209=) n.593G>C c.519G>C (p.Leu173=) n.422G>C | ClinVar dbSNP gnomAD v4 |
19 | g.55151873C>T | CA508989340 | TNNI3 | c.594G>A (p.Leu198=) c.627G>A (p.Leu209=) n.593G>A c.519G>A (p.Leu173=) n.422G>A | dbSNP |
19 | g.55151874A>C | CA407439521 | TNNI3 | c.593T>G (p.Leu198Arg) c.626T>G (p.Leu209Arg) n.592T>G c.518T>G (p.Leu173Arg) n.421T>G | |
19 | g.55151874A>G | CA407439523 | TNNI3 | c.593T>C (p.Leu198Pro) c.626T>C (p.Leu209Pro) n.592T>C c.518T>C (p.Leu173Pro) n.421T>C | |
19 | g.55151874A>T | CA407439525 | TNNI3 | c.593T>A (p.Leu198Gln) c.626T>A (p.Leu209Gln) n.592T>A c.518T>A (p.Leu173Gln) n.421T>A | |
19 | g.55151875G>A | CA508989342 | TNNI3 | c.592C>T (p.Leu198=) c.625C>T (p.Leu209=) n.591C>T c.517C>T (p.Leu173=) n.420C>T | dbSNP gnomAD v2 gnomAD v4 |
19 | g.55151875G>C | CA022019 | TNNI3 | c.592C>G (p.Leu198Val) c.625C>G (p.Leu209Val) n.591C>G c.517C>G (p.Leu173Val) n.420C>G | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.55151875G= | CA2343272548 | TNNI3 | c.592C= (p.Leu198=) c.625C= (p.Leu209=) n.591C= c.517C= (p.Leu173=) n.420C= | |
19 | g.55151875G>T | CA407439529 | TNNI3 | c.592C>A (p.Leu198Met) c.625C>A (p.Leu209Met) n.591C>A c.517C>A (p.Leu173Met) n.420C>A | |
19 | g.55151877_55151886del | CA2695229154 | TNNI3 | c.583_592del (p.Ile195Ter) c.616_625del (p.Ile206Ter) n.582_591del c.508_517del (p.Ile170Ter) n.411_420del | |
19 | g.55151876T>A | CA508989344 | TNNI3 | c.591A>T (p.Ala197=) c.624A>T (p.Ala208=) n.590A>T c.516A>T (p.Ala172=) n.419A>T | |
19 | g.55151876T>C | CA051909 | TNNI3 | c.591A>G (p.Ala197=) c.624A>G (p.Ala208=) n.590A>G c.516A>G (p.Ala172=) n.419A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151876T>G | CA508989343 | TNNI3 | c.591A>C (p.Ala197=) c.624A>C (p.Ala208=) n.590A>C c.516A>C (p.Ala172=) n.419A>C | |
19 | g.55151876T= | CA2343272553 | TNNI3 | c.591A= (p.Ala197=) c.624A= (p.Ala208=) n.590A= c.516A= (p.Ala172=) n.419A= | |
19 | g.55151877G>A | CA407439533 | TNNI3 | c.590C>T (p.Ala197Val) c.623C>T (p.Ala208Val) n.589C>T c.515C>T (p.Ala172Val) n.418C>T | dbSNP |
19 | g.55151877G>C | CA407439535 | TNNI3 | c.590C>G (p.Ala197Gly) c.623C>G (p.Ala208Gly) n.589C>G c.515C>G (p.Ala172Gly) n.418C>G | |
19 | g.55151877G= | CA2343272555 | TNNI3 | c.590C= (p.Ala197=) c.623C= (p.Ala208=) n.589C= c.515C= (p.Ala172=) n.418C= | |
19 | g.55151877G>T | CA407439537 | TNNI3 | c.590C>A (p.Ala197Glu) c.623C>A (p.Ala208Glu) n.589C>A c.515C>A (p.Ala172Glu) n.418C>A | |
19 | g.55151878C>A | CA407439539 | TNNI3 | c.589G>T (p.Ala197Ser) c.622G>T (p.Ala208Ser) n.588G>T c.514G>T (p.Ala172Ser) n.417G>T | |
19 | g.55151878C>G | CA407439542 | TNNI3 | c.589G>C (p.Ala197Pro) c.622G>C (p.Ala208Pro) n.588G>C c.514G>C (p.Ala172Pro) n.417G>C | |
19 | g.55151878C>T | CA407439544 | TNNI3 | c.589G>A (p.Ala197Thr) c.622G>A (p.Ala208Thr) n.588G>A c.514G>A (p.Ala172Thr) n.417G>A | |
19 | g.55151879A>C | CA407439547 | TNNI3 | c.588T>G (p.Asp196Glu) c.621T>G (p.Asp207Glu) n.587T>G c.513T>G (p.Asp171Glu) n.416T>G | |
19 | g.55151879A>G | CA508989345 | TNNI3 | c.588T>C (p.Asp196=) c.621T>C (p.Asp207=) n.587T>C c.513T>C (p.Asp171=) n.416T>C | ClinVar |
19 | g.55151879A>T | CA407439548 | TNNI3 | c.588T>A (p.Asp196Glu) c.621T>A (p.Asp207Glu) n.587T>A c.513T>A (p.Asp171Glu) n.416T>A | |
19 | g.55151880T>A | CA407439550 | TNNI3 | c.587A>T (p.Asp196Val) c.620A>T (p.Asp207Val) n.586A>T c.512A>T (p.Asp171Val) n.415A>T | |
19 | g.55151880T>C | CA407439552 | TNNI3 | c.587A>G (p.Asp196Gly) c.620A>G (p.Asp207Gly) n.586A>G c.512A>G (p.Asp171Gly) n.415A>G | ClinVar dbSNP |
19 | g.55151880T>G | CA407439554 | TNNI3 | c.587A>C (p.Asp196Ala) c.620A>C (p.Asp207Ala) n.586A>C c.512A>C (p.Asp171Ala) n.415A>C | gnomAD v4 |
19 | g.55151881C>A | CA022012 | TNNI3 | c.586G>T (p.Asp196Tyr) c.619G>T (p.Asp207Tyr) n.585G>T c.511G>T (p.Asp171Tyr) n.414G>T | ClinVar dbSNP gnomAD v4 |
19 | g.55151881C= | CA2343272564 | TNNI3 | c.586G= (p.Asp196=) c.619G= (p.Asp207=) n.585G= c.511G= (p.Asp171=) n.414G= | |
19 | g.55151881C>G | CA407439559 | TNNI3 | c.586G>C (p.Asp196His) c.619G>C (p.Asp207His) n.585G>C c.511G>C (p.Asp171His) n.414G>C | ClinVar |
19 | g.55151881C>T | CA022006 | TNNI3 | c.586G>A (p.Asp196Asn) c.619G>A (p.Asp207Asn) n.585G>A c.511G>A (p.Asp171Asn) n.414G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151882G>A | CA051883 | TNNI3 | c.585C>T (p.Ile195=) c.618C>T (p.Ile206=) n.584C>T c.510C>T (p.Ile170=) n.413C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151882G>C | CA407439563 | TNNI3 | c.585C>G (p.Ile195Met) c.618C>G (p.Ile206Met) n.584C>G c.510C>G (p.Ile170Met) n.413C>G | ClinVar dbSNP |
19 | g.55151882G= | CA2343272575 | TNNI3 | c.585C= (p.Ile195=) c.618C= (p.Ile206=) n.584C= c.510C= (p.Ile170=) n.413C= | |
19 | g.55151882G>T | CA508989346 | TNNI3 | c.585C>A (p.Ile195=) c.618C>A (p.Ile206=) n.584C>A c.510C>A (p.Ile170=) n.413C>A | gnomAD v4 |
19 | g.55151883A>C | CA407439565 | TNNI3 | c.584T>G (p.Ile195Ser) c.617T>G (p.Ile206Ser) n.583T>G c.509T>G (p.Ile170Ser) n.412T>G | |
19 | g.55151883A>G | CA407439567 | TNNI3 | c.584T>C (p.Ile195Thr) c.617T>C (p.Ile206Thr) n.583T>C c.509T>C (p.Ile170Thr) n.412T>C | COSMIC |
19 | g.55151883A>T | CA407439570 | TNNI3 | c.584T>A (p.Ile195Asn) c.617T>A (p.Ile206Asn) n.583T>A c.509T>A (p.Ile170Asn) n.412T>A | |
19 | g.55151884T>A | CA407439576 | TNNI3 | c.583A>T (p.Ile195Phe) c.616A>T (p.Ile206Phe) n.582A>T c.508A>T (p.Ile170Phe) n.411A>T | |
19 | g.55151884T>C | CA407439577 | TNNI3 | c.583A>G (p.Ile195Val) c.616A>G (p.Ile206Val) n.582A>G c.508A>G (p.Ile170Val) n.411A>G | |
19 | g.55151884T>G | CA10577114 | TNNI3 | c.583A>C (p.Ile195Leu) c.616A>C (p.Ile206Leu) n.582A>C c.508A>C (p.Ile170Leu) n.411A>C | ClinVar dbSNP |
19 | g.55151884T= | CA2343272581 | TNNI3 | c.583A= (p.Ile195=) c.616A= (p.Ile206=) n.582A= c.508A= (p.Ile170=) n.411A= | |
19 | g.55151885G>A | CA508989347 | TNNI3 | c.582C>T (p.Asn194=) c.615C>T (p.Asn205=) n.581C>T c.507C>T (p.Asn169=) n.410C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151885G>C | CA022000 | TNNI3 | c.582C>G (p.Asn194Lys) c.615C>G (p.Asn205Lys) n.581C>G c.507C>G (p.Asn169Lys) n.410C>G | ClinVar dbSNP |
19 | g.55151885G= | CA2343272587 | TNNI3 | c.582C= (p.Asn194=) c.615C= (p.Asn205=) n.581C= c.507C= (p.Asn169=) n.410C= | |
19 | g.55151885G>T | CA407439583 | TNNI3 | c.582C>A (p.Asn194Lys) c.615C>A (p.Asn205Lys) n.581C>A c.507C>A (p.Asn169Lys) n.410C>A | |
19 | g.55151886T>A | CA407439586 | TNNI3 | c.581A>T (p.Asn194Ile) c.614A>T (p.Asn205Ile) n.580A>T c.506A>T (p.Asn169Ile) n.409A>T | gnomAD v4 |
19 | g.55151886T>C | CA021995 | TNNI3 | c.581A>G (p.Asn194Ser) c.614A>G (p.Asn205Ser) n.580A>G c.506A>G (p.Asn169Ser) n.409A>G | ClinVar dbSNP |
19 | g.55151886T>G | CA051878 | TNNI3 | c.581A>C (p.Asn194Thr) c.614A>C (p.Asn205Thr) n.580A>C c.506A>C (p.Asn169Thr) n.409A>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151886T= | CA2343272594 | TNNI3 | c.581A= (p.Asn194=) c.614A= (p.Asn205=) n.580A= c.506A= (p.Asn169=) n.409A= | |
19 | g.55151887T>A | CA407439590 | TNNI3 | c.580A>T (p.Asn194Tyr) c.613A>T (p.Asn205Tyr) n.579A>T c.505A>T (p.Asn169Tyr) n.408A>T | |
19 | g.55151887T>C | CA407439592 | TNNI3 | c.580A>G (p.Asn194Asp) c.613A>G (p.Asn205Asp) n.579A>G c.505A>G (p.Asn169Asp) n.408A>G | ClinVar dbSNP |
19 | g.55151887T>G | CA407439595 | TNNI3 | c.580A>C (p.Asn194His) c.613A>C (p.Asn205His) n.579A>C c.505A>C (p.Asn169His) n.408A>C | |
19 | g.55151888C>A | CA021989 | TNNI3 | c.579G>T (p.Lys193Asn) c.612G>T (p.Lys204Asn) n.578G>T c.504G>T (p.Lys168Asn) n.407G>T | ClinVar dbSNP |
19 | g.55151888C= | CA2343272604 | TNNI3 | c.579G= (p.Lys193=) c.612G= (p.Lys204=) n.578G= c.504G= (p.Lys168=) n.407G= | |
19 | g.55151888C>G | CA021983 | TNNI3 | c.579G>C (p.Lys193Asn) c.612G>C (p.Lys204Asn) n.578G>C c.504G>C (p.Lys168Asn) n.407G>C | ClinVar dbSNP |
19 | g.55151888C>T | CA508989348 | TNNI3 | c.579G>A (p.Lys193=) c.612G>A (p.Lys204=) n.578G>A c.504G>A (p.Lys168=) n.407G>A | |
19 | g.55151889T>A | CA407439600 | TNNI3 | c.578A>T (p.Lys193Met) c.611A>T (p.Lys204Met) n.577A>T c.503A>T (p.Lys168Met) n.406A>T | |
19 | g.55151889T>C | CA407439603 | TNNI3 | c.578A>G (p.Lys193Arg) c.611A>G (p.Lys204Arg) n.577A>G c.503A>G (p.Lys168Arg) n.406A>G | ClinVar gnomAD v4 |
19 | g.55151889T>G | CA407439605 | TNNI3 | c.578A>C (p.Lys193Thr) c.611A>C (p.Lys204Thr) n.577A>C c.503A>C (p.Lys168Thr) n.406A>C | |
19 | g.55151890T>A | CA407439611 | TNNI3 | c.577A>T (p.Lys193Ter) c.610A>T (p.Lys204Ter) n.576A>T c.502A>T (p.Lys168Ter) n.405A>T | |
19 | g.55151890T>C | CA021977 | TNNI3 | c.577A>G (p.Lys193Glu) c.610A>G (p.Lys204Glu) n.576A>G c.502A>G (p.Lys168Glu) n.405A>G | ClinVar dbSNP |
19 | g.55151890T>G | CA407439608 | TNNI3 | c.577A>C (p.Lys193Gln) c.610A>C (p.Lys204Gln) n.576A>C c.502A>C (p.Lys168Gln) n.405A>C | dbSNP |
19 | g.55151890T= | CA2343272611 | TNNI3 | c.577A= (p.Lys193=) c.610A= (p.Lys204=) n.576A= c.502A= (p.Lys168=) n.405A= | |
19 | g.55151891G>A | CA508989349 | TNNI3 | c.576C>T (p.Arg192=) c.609C>T (p.Arg203=) n.575C>T c.501C>T (p.Arg167=) n.404C>T | gnomAD v4 |
19 | g.55151891G>C | CA508989350 | TNNI3 | c.576C>G (p.Arg192=) c.609C>G (p.Arg203=) n.575C>G c.501C>G (p.Arg167=) n.404C>G | |
19 | g.55151891G>T | CA508989351 | TNNI3 | c.576C>A (p.Arg192=) c.609C>A (p.Arg203=) n.575C>A c.501C>A (p.Arg167=) n.404C>A | |
19 | g.55151892C>A | CA021971 | TNNI3 | c.575G>T (p.Arg192Leu) c.608G>T (p.Arg203Leu) n.574G>T c.500G>T (p.Arg167Leu) n.403G>T | ClinVar dbSNP |
19 | g.55151892C= | CA2343272621 | TNNI3 | c.575G= (p.Arg192=) c.608G= (p.Arg203=) n.574G= c.500G= (p.Arg167=) n.403G= | |
19 | g.55151892C>G | CA021964 | TNNI3 | c.575G>C (p.Arg192Pro) c.608G>C (p.Arg203Pro) n.574G>C c.500G>C (p.Arg167Pro) n.403G>C | ClinVar dbSNP |
19 | g.55151892C>T | CA021957 | TNNI3 | c.575G>A (p.Arg192His) c.608G>A (p.Arg203His) n.574G>A c.500G>A (p.Arg167His) n.403G>A | ClinVar dbSNP gnomAD v4 COSMIC |
19 | g.55151893G>A | CA021951 | TNNI3 | c.574C>T (p.Arg192Cys) c.607C>T (p.Arg203Cys) n.573C>T c.499C>T (p.Arg167Cys) n.402C>T | ClinVar dbSNP COSMIC |
19 | g.55151893G>C | CA407439617 | TNNI3 | c.574C>G (p.Arg192Gly) c.607C>G (p.Arg203Gly) n.573C>G c.499C>G (p.Arg167Gly) n.402C>G | |
19 | g.55151893G= | CA2343272629 | TNNI3 | c.574C= (p.Arg192=) c.607C= (p.Arg203=) n.573C= c.499C= (p.Arg167=) n.402C= | |
19 | g.55151893G>T | CA407439618 | TNNI3 | c.574C>A (p.Arg192Ser) c.607C>A (p.Arg203Ser) n.573C>A c.499C>A (p.Arg167Ser) n.402C>A | |
19 | g.55151894C>A | CA407439620 | TNNI3 | c.573G>T (p.Trp191Cys) c.606G>T (p.Trp202Cys) n.572G>T c.498G>T (p.Trp166Cys) n.401G>T | dbSNP |
19 | g.55151894C>G | CA407439622 | TNNI3 | c.573G>C (p.Trp191Cys) c.606G>C (p.Trp202Cys) n.572G>C c.498G>C (p.Trp166Cys) n.401G>C | |
19 | g.55151894C>T | CA407439623 | TNNI3 | c.573G>A (p.Trp191Ter) c.606G>A (p.Trp202Ter) n.572G>A c.498G>A (p.Trp166Ter) n.401G>A | |
19 | g.55151895C>A | CA407439626 | TNNI3 | c.572G>T (p.Trp191Leu) c.605G>T (p.Trp202Leu) n.571G>T c.497G>T (p.Trp166Leu) n.400G>T | |
19 | g.55151895C= | CA2343272634 | TNNI3 | c.572G= (p.Trp191=) c.605G= (p.Trp202=) n.571G= c.497G= (p.Trp166=) n.400G= | |
19 | g.55151895C>G | CA407439627 | TNNI3 | c.572G>C (p.Trp191Ser) c.605G>C (p.Trp202Ser) n.571G>C c.497G>C (p.Trp166Ser) n.400G>C | |
19 | g.55151895C>T | CA310144922 | TNNI3 | c.572G>A (p.Trp191Ter) c.605G>A (p.Trp202Ter) n.571G>A c.497G>A (p.Trp166Ter) n.400G>A | dbSNP |
19 | g.55151896A>C | CA407439630 | TNNI3 | c.571T>G (p.Trp191Gly) c.604T>G (p.Trp202Gly) n.570T>G c.496T>G (p.Trp166Gly) n.399T>G | |
19 | g.55151896A>G | CA407439631 | TNNI3 | c.571T>C (p.Trp191Arg) c.604T>C (p.Trp202Arg) n.570T>C c.496T>C (p.Trp166Arg) n.399T>C | |
19 | g.55151896A>T | CA407439633 | TNNI3 | c.571T>A (p.Trp191Arg) c.604T>A (p.Trp202Arg) n.570T>A c.496T>A (p.Trp166Arg) n.399T>A | |
19 | g.55151897G>A | CA508989352 | TNNI3 | c.570C>T (p.Asp190=) c.603C>T (p.Asp201=) n.569C>T c.495C>T (p.Asp165=) n.398C>T | ClinVar dbSNP |
19 | g.55151897G>C | CA407439634 | TNNI3 | c.570C>G (p.Asp190Glu) c.603C>G (p.Asp201Glu) n.569C>G c.495C>G (p.Asp165Glu) n.398C>G | ClinVar dbSNP |
19 | g.55151897G= | CA2343272637 | TNNI3 | c.570C= (p.Asp190=) c.603C= (p.Asp201=) n.569C= c.495C= (p.Asp165=) n.398C= | |
19 | g.55151897G>T | CA407439636 | TNNI3 | c.570C>A (p.Asp190Glu) c.603C>A (p.Asp201Glu) n.569C>A c.495C>A (p.Asp165Glu) n.398C>A | |
19 | g.55151897_55151904delinsGTCTCCCA | CA2343272640 | TNNI3 | c.563_570delinsTGGGAGAC (p.Val188=) c.596_603delinsTGGGAGAC (p.Val199=) n.562_569delinsTGGGAGAC c.488_495delinsTGGGAGAC (p.Val163=) n.391_398delinsTGGGAGAC | |
19 | g.55151898T>A | CA407439639 | TNNI3 | c.569A>T (p.Asp190Val) c.602A>T (p.Asp201Val) n.568A>T c.494A>T (p.Asp165Val) n.397A>T | |
19 | g.55151898T>C | CA021945 | TNNI3 | c.569A>G (p.Asp190Gly) c.602A>G (p.Asp201Gly) n.568A>G c.494A>G (p.Asp165Gly) n.397A>G | ClinVar dbSNP |
19 | g.55151898T>G | CA407439642 | TNNI3 | c.569A>C (p.Asp190Ala) c.602A>C (p.Asp201Ala) n.568A>C c.494A>C (p.Asp165Ala) n.397A>C | |
19 | g.55151898T= | CA2343272645 | TNNI3 | c.569A= (p.Asp190=) c.602A= (p.Asp201=) n.568A= c.494A= (p.Asp165=) n.397A= | |
19 | g.55151898_55151904del | CA2343272643 | TNNI3 | c.563_569del (p.Val188AlafsTer9) c.596_602del (p.Val199AlafsTer9) n.562_568del c.488_494del (p.Val163AlafsTer9) n.391_397del | ClinVar dbSNP |
19 | g.55151899C>A | CA021939 | TNNI3 | c.568G>T (p.Asp190Tyr) c.601G>T (p.Asp201Tyr) n.567G>T c.493G>T (p.Asp165Tyr) n.396G>T | ClinVar dbSNP |
19 | g.55151899C= | CA2343272647 | TNNI3 | c.568G= (p.Asp190=) c.601G= (p.Asp201=) n.567G= c.493G= (p.Asp165=) n.396G= | |
19 | g.55151899C>G | CA407439646 | TNNI3 | c.568G>C (p.Asp190His) c.601G>C (p.Asp201His) n.567G>C c.493G>C (p.Asp165His) n.396G>C | |
19 | g.55151899C>T | CA407439648 | TNNI3 | c.568G>A (p.Asp190Asn) c.601G>A (p.Asp201Asn) n.567G>A c.493G>A (p.Asp165Asn) n.396G>A | |
19 | g.55151900T>A | CA508989353 | TNNI3 | c.567A>T (p.Gly189=) c.600A>T (p.Gly200=) n.566A>T c.492A>T (p.Gly164=) n.395A>T | |
19 | g.55151900T>C | CA310144932 | TNNI3 | c.567A>G (p.Gly189=) c.600A>G (p.Gly200=) n.566A>G c.492A>G (p.Gly164=) n.395A>G | ClinVar dbSNP |
19 | g.55151900T>G | CA508989354 | TNNI3 | c.567A>C (p.Gly189=) c.600A>C (p.Gly200=) n.566A>C c.492A>C (p.Gly164=) n.395A>C | |
19 | g.55151900T= | CA2343272650 | TNNI3 | c.567A= (p.Gly189=) c.600A= (p.Gly200=) n.566A= c.492A= (p.Gly164=) n.395A= | |
19 | g.55151901C>A | CA407439651 | TNNI3 | c.566G>T (p.Gly189Val) c.599G>T (p.Gly200Val) n.565G>T c.491G>T (p.Gly164Val) n.394G>T | |
19 | g.55151901C= | CA2343272651 | TNNI3 | c.566G= (p.Gly189=) c.599G= (p.Gly200=) n.565G= c.491G= (p.Gly164=) n.394G= | |
19 | g.55151901C>G | CA407439652 | TNNI3 | c.566G>C (p.Gly189Ala) c.599G>C (p.Gly200Ala) n.565G>C c.491G>C (p.Gly164Ala) n.394G>C | ClinVar |
19 | g.55151901C>T | CA021932 | TNNI3 | c.566G>A (p.Gly189Glu) c.599G>A (p.Gly200Glu) n.565G>A c.491G>A (p.Gly164Glu) n.394G>A | ClinVar dbSNP gnomAD v4 |
19 | g.55151902C>A | CA407439653 | TNNI3 | c.565G>T (p.Gly189Ter) c.598G>T (p.Gly200Ter) n.564G>T c.490G>T (p.Gly164Ter) n.393G>T | |
19 | g.55151902C>G | CA407439654 | TNNI3 | c.565G>C (p.Gly189Arg) c.598G>C (p.Gly200Arg) n.564G>C c.490G>C (p.Gly164Arg) n.393G>C | |
19 | g.55151902C>T | CA407439656 | TNNI3 | c.565G>A (p.Gly189Arg) c.598G>A (p.Gly200Arg) n.564G>A c.490G>A (p.Gly164Arg) n.393G>A | gnomAD v4 |
19 | g.55151903C>A | CA508989355 | TNNI3 | c.564G>T (p.Val188=) c.597G>T (p.Val199=) n.563G>T c.489G>T (p.Val163=) n.392G>T | COSMIC |
19 | g.55151903C= | CA2343272652 | TNNI3 | c.564G= (p.Val188=) c.597G= (p.Val199=) n.563G= c.489G= (p.Val163=) n.392G= | |
19 | g.55151903C>G | CA508989356 | TNNI3 | c.564G>C (p.Val188=) c.597G>C (p.Val199=) n.563G>C c.489G>C (p.Val163=) n.392G>C | |
19 | g.55151903C>T | CA051861 | TNNI3 | c.564G>A (p.Val188=) c.597G>A (p.Val199=) n.563G>A c.489G>A (p.Val163=) n.392G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151904A= | CA2343272653 | TNNI3 | c.563T= (p.Val188=) c.596T= (p.Val199=) n.562T= c.488T= (p.Val163=) n.391T= | |
19 | g.55151904A>C | CA407439660 | TNNI3 | c.563T>G (p.Val188Gly) c.596T>G (p.Val199Gly) n.562T>G c.488T>G (p.Val163Gly) n.391T>G | dbSNP |
19 | g.55151904A>G | CA407439657 | TNNI3 | c.563T>C (p.Val188Ala) c.596T>C (p.Val199Ala) n.562T>C c.488T>C (p.Val163Ala) n.391T>C | |
19 | g.55151904A>T | CA407439658 | TNNI3 | c.563T>A (p.Val188Glu) c.596T>A (p.Val199Glu) n.562T>A c.488T>A (p.Val163Glu) n.391T>A | |
19 | g.55151905C>A | CA021928 | TNNI3 | c.562G>T (p.Val188Leu) c.595G>T (p.Val199Leu) n.561G>T c.487G>T (p.Val163Leu) n.390G>T | ClinVar dbSNP gnomAD v4 |
19 | g.55151905C= | CA2343272654 | TNNI3 | c.562G= (p.Val188=) c.595G= (p.Val199=) n.561G= c.487G= (p.Val163=) n.390G= | |
19 | g.55151905C>G | CA407439663 | TNNI3 | c.562G>C (p.Val188Leu) c.595G>C (p.Val199Leu) n.561G>C c.487G>C (p.Val163Leu) n.390G>C | gnomAD v4 |
19 | g.55151905C>T | CA021922 | TNNI3 | c.562G>A (p.Val188Met) c.595G>A (p.Val199Met) n.561G>A c.487G>A (p.Val163Met) n.390G>A | ClinVar dbSNP gnomAD v4 |
19 | g.55151906C>A | CA051855 | TNNI3 | c.561G>T (p.Glu187Asp) c.594G>T (p.Glu198Asp) n.560G>T c.486G>T (p.Glu162Asp) n.389G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151906C= | CA2343272655 | TNNI3 | c.561G= (p.Glu187=) c.594G= (p.Glu198=) n.560G= c.486G= (p.Glu162=) n.389G= | |
19 | g.55151906C>G | CA407439665 | TNNI3 | c.561G>C (p.Glu187Asp) c.594G>C (p.Glu198Asp) n.560G>C c.486G>C (p.Glu162Asp) n.389G>C | gnomAD v4 |
19 | g.55151906C>T | CA508989357 | TNNI3 | c.561G>A (p.Glu187=) c.594G>A (p.Glu198=) n.560G>A c.486G>A (p.Glu162=) n.389G>A | |
19 | g.55151907T>A | CA407439666 | TNNI3 | c.560A>T (p.Glu187Val) c.593A>T (p.Glu198Val) n.559A>T c.485A>T (p.Glu162Val) n.388A>T | |
19 | g.55151907T>C | CA407439668 | TNNI3 | c.560A>G (p.Glu187Gly) c.593A>G (p.Glu198Gly) n.559A>G c.485A>G (p.Glu162Gly) n.388A>G | COSMIC |
19 | g.55151907T>G | CA407439669 | TNNI3 | c.560A>C (p.Glu187Ala) c.593A>C (p.Glu198Ala) n.559A>C c.485A>C (p.Glu162Ala) n.388A>C | |
19 | g.55151907_55151908delinsCT | CA2343272657 | TNNI3 | c.559_560delinsAG (p.Glu187Arg) c.592_593delinsAG (p.Glu198Arg) n.558_559delinsAG c.484_485delinsAG (p.Glu162Arg) n.387_388delinsAG | ClinVar dbSNP |
19 | g.55151907_55151908delinsTC | CA2343272656 | TNNI3 | c.559_560delinsGA (p.Glu187=) c.592_593delinsGA (p.Glu198=) n.558_559delinsGA c.484_485delinsGA (p.Glu162=) n.387_388delinsGA | |
19 | g.55151908C>A | CA407439670 | TNNI3 | c.559G>T (p.Glu187Ter) c.592G>T (p.Glu198Ter) n.558G>T c.484G>T (p.Glu162Ter) n.387G>T | |
19 | g.55151908C= | CA2343272658 | TNNI3 | c.559G= (p.Glu187=) c.592G= (p.Glu198=) n.558G= c.484G= (p.Glu162=) n.387G= | |
19 | g.55151908C>G | CA407439671 | TNNI3 | c.559G>C (p.Glu187Gln) c.592G>C (p.Glu198Gln) n.558G>C c.484G>C (p.Glu162Gln) n.387G>C | |
19 | g.55151908C>T | CA021916 | TNNI3 | c.559G>A (p.Glu187Lys) c.592G>A (p.Glu198Lys) n.558G>A c.484G>A (p.Glu162Lys) n.387G>A | ClinVar dbSNP |
19 | g.55151909C>A | CA508989358 | TNNI3 | c.558G>T (p.Arg186=) c.591G>T (p.Arg197=) n.557G>T c.483G>T (p.Arg161=) n.386G>T | |
19 | g.55151909C>G | CA508989359 | TNNI3 | c.558G>C (p.Arg186=) c.591G>C (p.Arg197=) n.557G>C c.483G>C (p.Arg161=) n.386G>C | |
19 | g.55151909C>T | CA508989360 | TNNI3 | c.558G>A (p.Arg186=) c.591G>A (p.Arg197=) n.557G>A c.483G>A (p.Arg161=) n.386G>A | COSMIC |
19 | g.55151910C>A | CA407439673 | TNNI3 | c.557G>T (p.Arg186Leu) c.590G>T (p.Arg197Leu) n.556G>T c.482G>T (p.Arg161Leu) n.385G>T | |
19 | g.55151910C= | CA2343272659 | TNNI3 | c.557G= (p.Arg186=) c.590G= (p.Arg197=) n.556G= c.482G= (p.Arg161=) n.385G= | |
19 | g.55151910C>G | CA407439675 | TNNI3 | c.557G>C (p.Arg186Pro) c.590G>C (p.Arg197Pro) n.556G>C c.482G>C (p.Arg161Pro) n.385G>C | |
19 | g.55151910C>T | CA021907 | TNNI3 | c.557G>A (p.Arg186Gln) c.590G>A (p.Arg197Gln) n.556G>A c.482G>A (p.Arg161Gln) n.385G>A | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.55151911G>A | CA051839 | TNNI3 | c.556C>T (p.Arg186Trp) c.589C>T (p.Arg197Trp) n.555C>T c.481C>T (p.Arg161Trp) n.384C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
19 | g.55151911G>C | CA407439677 | TNNI3 | c.556C>G (p.Arg186Gly) c.589C>G (p.Arg197Gly) n.555C>G c.481C>G (p.Arg161Gly) n.384C>G | |
19 | g.55151911G= | CA2343272660 | TNNI3 | c.556C= (p.Arg186=) c.589C= (p.Arg197=) n.555C= c.481C= (p.Arg161=) n.384C= | |
19 | g.55151911G>T | CA508989361 | TNNI3 | c.556C>A (p.Arg186=) c.589C>A (p.Arg197=) n.555C>A c.481C>A (p.Arg161=) n.384C>A | ClinVar gnomAD v4 |
19 | g.55151912G>A | CA508989362 | TNNI3 | c.555C>T (p.Asn185=) c.588C>T (p.Asn196=) n.554C>T c.480C>T (p.Asn160=) n.383C>T | |
19 | g.55151912G>C | CA021902 | TNNI3 | c.555C>G (p.Asn185Lys) c.588C>G (p.Asn196Lys) n.554C>G c.480C>G (p.Asn160Lys) n.383C>G | ClinVar dbSNP |
19 | g.55151912G= | CA2343272661 | TNNI3 | c.555C= (p.Asn185=) c.588C= (p.Asn196=) n.554C= c.480C= (p.Asn160=) n.383C= | |
19 | g.55151912G>T | CA407439680 | TNNI3 | c.555C>A (p.Asn185Lys) c.588C>A (p.Asn196Lys) n.554C>A c.480C>A (p.Asn160Lys) n.383C>A | |
19 | g.55151913T>A | CA407439681 | TNNI3 | c.554A>T (p.Asn185Ile) c.587A>T (p.Asn196Ile) n.553A>T c.479A>T (p.Asn160Ile) n.382A>T | |
19 | g.55151913T>C | CA021896 | TNNI3 | c.554A>G (p.Asn185Ser) c.587A>G (p.Asn196Ser) n.553A>G c.479A>G (p.Asn160Ser) n.382A>G | ClinVar dbSNP |
19 | g.55151913T>G | CA407439684 | TNNI3 | c.554A>C (p.Asn185Thr) c.587A>C (p.Asn196Thr) n.553A>C c.479A>C (p.Asn160Thr) n.382A>C | |
19 | g.55151913T= | CA2343272662 | TNNI3 | c.554A= (p.Asn185=) c.587A= (p.Asn196=) n.553A= c.479A= (p.Asn160=) n.382A= | |
19 | g.55151916del | CA2695229155 | TNNI3 | c.554del (p.Asn185ThrfsTer14) c.587del (p.Asn196ThrfsTer14) n.553del c.479del (p.Asn160ThrfsTer14) n.382del | |
19 | g.55151914T>A | CA021890 | TNNI3 | c.553A>T (p.Asn185Tyr) c.586A>T (p.Asn196Tyr) n.552A>T c.478A>T (p.Asn160Tyr) n.381A>T | ClinVar dbSNP |
19 | g.55151914T>C | CA407439686 | TNNI3 | c.553A>G (p.Asn185Asp) c.586A>G (p.Asn196Asp) n.552A>G c.478A>G (p.Asn160Asp) n.381A>G | |
19 | g.55151914T>G | CA407439687 | TNNI3 | c.553A>C (p.Asn185His) c.586A>C (p.Asn196His) n.552A>C c.478A>C (p.Asn160His) n.381A>C | |
19 | g.55151914T= | CA2343272663 | TNNI3 | c.553A= (p.Asn185=) c.586A= (p.Asn196=) n.552A= c.478A= (p.Asn160=) n.381A= | |
19 | g.55151915T>A | CA407439689 | TNNI3 | c.552A>T (p.Glu184Asp) c.585A>T (p.Glu195Asp) n.551A>T c.477A>T (p.Glu159Asp) n.380A>T | |
19 | g.55151915T>C | CA508989363 | TNNI3 | c.552A>G (p.Glu184=) c.585A>G (p.Glu195=) n.551A>G c.477A>G (p.Glu159=) n.380A>G | |
19 | g.55151915T>G | CA407439690 | TNNI3 | c.552A>C (p.Glu184Asp) c.585A>C (p.Glu195Asp) n.551A>C c.477A>C (p.Glu159Asp) n.380A>C | |
19 | g.55151916T>A | CA407439692 | TNNI3 | c.551A>T (p.Glu184Val) c.584A>T (p.Glu195Val) n.550A>T c.476A>T (p.Glu159Val) n.379A>T | |
19 | g.55151916T>C | CA407439694 | TNNI3 | c.551A>G (p.Glu184Gly) c.584A>G (p.Glu195Gly) n.550A>G c.476A>G (p.Glu159Gly) n.379A>G | |
19 | g.55151916T>G | CA407439695 | TNNI3 | c.551A>C (p.Glu184Ala) c.584A>C (p.Glu195Ala) n.550A>C c.476A>C (p.Glu159Ala) n.379A>C | |
19 | g.55151917C>A | CA407439697 | TNNI3 | c.550G>T (p.Glu184Ter) c.583G>T (p.Glu195Ter) n.549G>T c.475G>T (p.Glu159Ter) n.378G>T | |
19 | g.55151917C= | CA2343272664 | TNNI3 | c.550G= (p.Glu184=) c.583G= (p.Glu195=) n.549G= c.475G= (p.Glu159=) n.378G= | |
19 | g.55151917C>G | CA407439699 | TNNI3 | c.550G>C (p.Glu184Gln) c.583G>C (p.Glu195Gln) n.549G>C c.475G>C (p.Glu159Gln) n.378G>C | ClinVar dbSNP |
19 | g.55151917C>T | CA021885 | TNNI3 | c.550G>A (p.Glu184Lys) c.583G>A (p.Glu195Lys) n.549G>A c.475G>A (p.Glu159Lys) n.378G>A | ClinVar dbSNP |
19 | g.55151918C>A | CA407439701 | TNNI3 | c.550-1G>T (n.550-1G>T) c.583-1G>T (n.583-1G>T) n.549-1G>T c.475-1G>T (n.475-1G>T) n.378-1G>T | |
19 | g.55151918C= | CA2343272665 | TNNI3 | c.550-1G= (n.550-1G=) c.583-1G= (n.583-1G=) n.549-1G= c.475-1G= (n.475-1G=) n.378-1G= | |
19 | g.55151918C>G | CA407439704 | TNNI3 | c.550-1G>C (n.550-1G>C) c.583-1G>C (n.583-1G>C) n.549-1G>C c.475-1G>C (n.475-1G>C) n.378-1G>C | |
19 | g.55151918C>T | CA407439702 | TNNI3 | c.550-1G>A (n.550-1G>A) c.583-1G>A (n.583-1G>A) n.549-1G>A c.475-1G>A (n.475-1G>A) n.378-1G>A | ClinVar dbSNP COSMIC |
19 | g.55151919T>A | CA407439706 | TNNI3 | c.550-2A>T (n.550-2A>T) c.583-2A>T (n.583-2A>T) n.549-2A>T c.475-2A>T (n.475-2A>T) n.378-2A>T | ClinVar dbSNP |
19 | g.55151919T>C | CA407439707 | TNNI3 | c.550-2A>G (n.550-2A>G) c.583-2A>G (n.583-2A>G) n.549-2A>G c.475-2A>G (n.475-2A>G) n.378-2A>G | |
19 | g.55151919T>G | CA407439709 | TNNI3 | c.550-2A>C (n.550-2A>C) c.583-2A>C (n.583-2A>C) n.549-2A>C c.475-2A>C (n.475-2A>C) n.378-2A>C | gnomAD v4 |
19 | g.55151920G>C | CA310144959 | TNNI3 | c.550-3C>G (n.550-3C>G) c.583-3C>G (n.583-3C>G) n.549-3C>G c.475-3C>G (n.475-3C>G) n.378-3C>G | dbSNP |
19 | g.55151920G= | CA2343272666 | TNNI3 | c.550-3C= (n.550-3C=) c.583-3C= (n.583-3C=) n.549-3C= c.475-3C= (n.475-3C=) n.378-3C= | |
19 | g.55151920G>T | CA310144962 | TNNI3 | c.550-3C>A (n.550-3C>A) c.583-3C>A (n.583-3C>A) n.549-3C>A c.475-3C>A (n.475-3C>A) n.378-3C>A | dbSNP |
19 | g.55151923G>A | CA2587243161 | TNNI3 | c.550-6C>T (n.550-6C>T) c.583-6C>T (n.583-6C>T) n.549-6C>T c.475-6C>T (n.475-6C>T) n.378-6C>T | ClinVar gnomAD v4 |
19 | g.55151924G>A | CA2587243162 | TNNI3 | c.550-7C>T (n.550-7C>T) c.583-7C>T (n.583-7C>T) n.549-7C>T c.475-7C>T (n.475-7C>T) n.378-7C>T | gnomAD v4 |
19 | g.55151925A= | CA2343272667 | TNNI3 | c.550-8T= (n.550-8T=) c.583-8T= (n.583-8T=) n.549-8T= c.475-8T= (n.475-8T=) n.378-8T= | |
19 | g.55151925A>G | CA2587243163 | TNNI3 | c.550-8T>C (n.550-8T>C) c.583-8T>C (n.583-8T>C) n.549-8T>C c.475-8T>C (n.475-8T>C) n.378-8T>C | gnomAD v4 |
19 | g.55151925A>T | CA051830 | TNNI3 | c.550-8T>A (n.550-8T>A) c.583-8T>A (n.583-8T>A) n.549-8T>A c.475-8T>A (n.475-8T>A) n.378-8T>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151925_55151930delinsATGGCG | CA2343272668 | TNNI3 | c.550-13_550-8delinsCGCCAT (n.550-13_550-8delinsCGCCAT) c.583-13_583-8delinsCGCCAT (n.583-13_583-8delinsCGCCAT) n.549-13_549-8delinsCGCCAT c.475-13_475-8delinsCGCCAT (n.475-13_475-8delinsCGCCAT) n.378-13_378-8delinsCGCCAT | |
19 | g.55151926_55151930del | CA2343272669 | TNNI3 | c.550-13_550-9del (n.550-13_550-9del) c.583-13_583-9del (n.583-13_583-9del) n.549-13_549-9del c.475-13_475-9del (n.475-13_475-9del) n.378-13_378-9del | dbSNP |
19 | g.55151927G>A | CA021879 | TNNI3 | c.550-10C>T (n.550-10C>T) c.583-10C>T (n.583-10C>T) n.549-10C>T c.475-10C>T (n.475-10C>T) n.378-10C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151927G= | CA2343272670 | TNNI3 | c.550-10C= (n.550-10C=) c.583-10C= (n.583-10C=) n.549-10C= c.475-10C= (n.475-10C=) n.378-10C= | |
19 | g.55151928G>A | CA10649138 | TNNI3 | c.550-11C>T (n.550-11C>T) c.583-11C>T (n.583-11C>T) n.549-11C>T c.475-11C>T (n.475-11C>T) n.378-11C>T | ClinVar dbSNP gnomAD v3 gnomAD v4 |
19 | g.55151928G= | CA2343272671 | TNNI3 | c.550-11C= (n.550-11C=) c.583-11C= (n.583-11C=) n.549-11C= c.475-11C= (n.475-11C=) n.378-11C= | |
19 | g.55151929C>A | CA633870498 | TNNI3 | c.550-12G>T (n.550-12G>T) c.583-12G>T (n.583-12G>T) n.549-12G>T c.475-12G>T (n.475-12G>T) n.378-12G>T | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151929C= | CA2343272672 | TNNI3 | c.550-12G= (n.550-12G=) c.583-12G= (n.583-12G=) n.549-12G= c.475-12G= (n.475-12G=) n.378-12G= | |
19 | g.55151929C>T | CA051748 | TNNI3 | c.550-12G>A (n.550-12G>A) c.583-12G>A (n.583-12G>A) n.549-12G>A c.475-12G>A (n.475-12G>A) n.378-12G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151930G>A | CA051759 | TNNI3 | c.550-13C>T (n.550-13C>T) c.583-13C>T (n.583-13C>T) n.549-13C>T c.475-13C>T (n.475-13C>T) n.378-13C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
19 | g.55151930G>C | CA051751 | TNNI3 | c.550-13C>G (n.550-13C>G) c.583-13C>G (n.583-13C>G) n.549-13C>G c.475-13C>G (n.475-13C>G) n.378-13C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
19 | g.55151930G= | CA2343272673 | TNNI3 | c.550-13C= (n.550-13C=) c.583-13C= (n.583-13C=) n.549-13C= c.475-13C= (n.475-13C=) n.378-13C= | |
19 | g.55151931A= | CA2343272674 | TNNI3 | c.550-14T= (n.550-14T=) c.583-14T= (n.583-14T=) n.549-14T= c.475-14T= (n.475-14T=) n.378-14T= | |
19 | g.55151931A>G | CA051770 | TNNI3 | c.550-14T>C (n.550-14T>C) c.583-14T>C (n.583-14T>C) n.549-14T>C c.475-14T>C (n.475-14T>C) n.378-14T>C | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
19 | g.55151931A>T | CA2576892607 | TNNI3 | c.550-14T>A (n.550-14T>A) c.583-14T>A (n.583-14T>A) n.549-14T>A c.475-14T>A (n.475-14T>A) n.378-14T>A | |
19 | g.55151932T>G | CA2343272676 | TNNI3 | c.550-15A>C (n.550-15A>C) c.583-15A>C (n.583-15A>C) n.549-15A>C c.475-15A>C (n.475-15A>C) n.378-15A>C | dbSNP |
19 | g.55151932T= | CA2343272675 | TNNI3 | c.550-15A= (n.550-15A=) c.583-15A= (n.583-15A=) n.549-15A= c.475-15A= (n.475-15A=) n.378-15A= | |
19 | g.55151933G>A | CA2343272678 | TNNI3 | c.550-16C>T (n.550-16C>T) c.583-16C>T (n.583-16C>T) n.549-16C>T c.475-16C>T (n.475-16C>T) n.378-16C>T | dbSNP |
19 | g.55151933G= | CA2343272677 | TNNI3 | c.550-16C= (n.550-16C=) c.583-16C= (n.583-16C=) n.549-16C= c.475-16C= (n.475-16C=) n.378-16C= | |
19 | g.55151935G>A | CA2587243175 | TNNI3 | c.550-18C>T (n.550-18C>T) c.583-18C>T (n.583-18C>T) n.549-18C>T c.475-18C>T (n.475-18C>T) n.378-18C>T | gnomAD v4 |
19 | g.55151935G>T | CA2587243176 | TNNI3 | c.550-18C>A (n.550-18C>A) c.583-18C>A (n.583-18C>A) n.549-18C>A c.475-18C>A (n.475-18C>A) n.378-18C>A | gnomAD v4 |
19 | g.55151936T>C | CA2587243177 | TNNI3 | c.550-19A>G (n.550-19A>G) c.583-19A>G (n.583-19A>G) n.549-19A>G c.475-19A>G (n.475-19A>G) n.378-19A>G | gnomAD v4 |
19 | g.55151937C= | CA2343272679 | TNNI3 | c.550-20G= (n.550-20G=) c.583-20G= (n.583-20G=) n.549-20G= c.475-20G= (n.475-20G=) n.378-20G= | |
19 | g.55151938A>G | CA2587243179 | TNNI3 | c.550-21T>C (n.550-21T>C) c.583-21T>C (n.583-21T>C) n.549-21T>C c.475-21T>C (n.475-21T>C) n.378-21T>C | gnomAD v4 |
19 | g.55151938dup | CA997245871 | TNNI3 | c.550-21dup (n.550-21dup) c.583-21dup (n.583-21dup) n.549-21dup c.475-21dup (n.475-21dup) n.378-21dup | dbSNP gnomAD v3 gnomAD v4 |
19 | g.55151940_55151941del | CA2576892608 | TNNI3 | c.550-22_550-21del (n.550-22_550-21del) c.583-22_583-21del (n.583-22_583-21del) n.549-22_549-21del c.475-22_475-21del (n.475-22_475-21del) n.378-22_378-21del | |
19 | g.55151939G>C | CA2587243180 | TNNI3 | c.550-22C>G (n.550-22C>G) c.583-22C>G (n.583-22C>G) n.549-22C>G c.475-22C>G (n.475-22C>G) n.378-22C>G | gnomAD v4 |
19 | g.55151940A= | CA2343272680 | TNNI3 | c.550-23T= (n.550-23T=) c.583-23T= (n.583-23T=) n.549-23T= c.475-23T= (n.475-23T=) n.378-23T= | |
19 | g.55151940A>C | CA051773 | TNNI3 | c.550-23T>G (n.550-23T>G) c.583-23T>G (n.583-23T>G) n.549-23T>G c.475-23T>G (n.475-23T>G) n.378-23T>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |