| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.113089518T>A | CA378532847 | TCF7L2 | c.483+49392T>A (n.483+49392T>A) c.552+49392T>A (n.552+49392T>A) c.602T>A (p.Val201Asp) c.512T>A (p.Val171Asp) c.605T>A (p.Val202Asp) c.382-51666T>A (n.382-51666T>A) c.287T>A (p.Val96Asp) c.674T>A (p.Val225Asp) c.671T>A (p.Val224Asp) c.215T>A (p.Val72Asp) | |
| 10 | g.113089518T>C | CA378532845 | TCF7L2 | c.483+49392T>C (n.483+49392T>C) c.552+49392T>C (n.552+49392T>C) c.602T>C (p.Val201Ala) c.512T>C (p.Val171Ala) c.605T>C (p.Val202Ala) c.382-51666T>C (n.382-51666T>C) c.287T>C (p.Val96Ala) c.674T>C (p.Val225Ala) c.671T>C (p.Val224Ala) c.215T>C (p.Val72Ala) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 10 | g.113089518T>G | CA378532846 | TCF7L2 | c.483+49392T>G (n.483+49392T>G) c.552+49392T>G (n.552+49392T>G) c.602T>G (p.Val201Gly) c.512T>G (p.Val171Gly) c.605T>G (p.Val202Gly) c.382-51666T>G (n.382-51666T>G) c.287T>G (p.Val96Gly) c.674T>G (p.Val225Gly) c.671T>G (p.Val224Gly) c.215T>G (p.Val72Gly) | |
| 10 | g.113089518T= | CA1937197477 | TCF7L2 | c.483+49392T= (n.483+49392T=) c.552+49392T= (n.552+49392T=) c.602T= (p.Val201=) c.512T= (p.Val171=) c.605T= (p.Val202=) c.382-51666T= (n.382-51666T=) c.287T= (p.Val96=) c.674T= (p.Val225=) c.671T= (p.Val224=) c.215T= (p.Val72=) | |
| 10 | g.113089519T>A | CA596094337 | TCF7L2 | c.483+49393T>A (n.483+49393T>A) c.552+49393T>A (n.552+49393T>A) c.603T>A (p.Val201=) c.513T>A (p.Val171=) c.606T>A (p.Val202=) c.382-51665T>A (n.382-51665T>A) c.288T>A (p.Val96=) c.675T>A (p.Val225=) c.672T>A (p.Val224=) c.216T>A (p.Val72=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.113089519T= | CA1937197478 | TCF7L2 | c.483+49393T= (n.483+49393T=) c.552+49393T= (n.552+49393T=) c.603T= (p.Val201=) c.513T= (p.Val171=) c.606T= (p.Val202=) c.382-51665T= (n.382-51665T=) c.288T= (p.Val96=) c.675T= (p.Val225=) c.672T= (p.Val224=) c.216T= (p.Val72=) | |
| 10 | g.113089520G>A | CA378532848 | TCF7L2 | c.483+49394G>A (n.483+49394G>A) c.552+49394G>A (n.552+49394G>A) c.604G>A (p.Gly202Arg) c.514G>A (p.Gly172Arg) c.607G>A (p.Gly203Arg) c.382-51664G>A (n.382-51664G>A) c.289G>A (p.Gly97Arg) c.676G>A (p.Gly226Arg) c.673G>A (p.Gly225Arg) c.217G>A (p.Gly73Arg) | |
| 10 | g.113089520G>C | CA5692913 | TCF7L2 | c.483+49394G>C (n.483+49394G>C) c.552+49394G>C (n.552+49394G>C) c.604G>C (p.Gly202Arg) c.514G>C (p.Gly172Arg) c.607G>C (p.Gly203Arg) c.382-51664G>C (n.382-51664G>C) c.289G>C (p.Gly97Arg) c.676G>C (p.Gly226Arg) c.673G>C (p.Gly225Arg) c.217G>C (p.Gly73Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.113089520G= | CA1937197479 | TCF7L2 | c.483+49394G= (n.483+49394G=) c.552+49394G= (n.552+49394G=) c.604G= (p.Gly202=) c.514G= (p.Gly172=) c.607G= (p.Gly203=) c.382-51664G= (n.382-51664G=) c.289G= (p.Gly97=) c.676G= (p.Gly226=) c.673G= (p.Gly225=) c.217G= (p.Gly73=) | |
| 10 | g.113089520G>T | CA378532849 | TCF7L2 | c.483+49394G>T (n.483+49394G>T) c.552+49394G>T (n.552+49394G>T) c.604G>T (p.Gly202Trp) c.514G>T (p.Gly172Trp) c.607G>T (p.Gly203Trp) c.382-51664G>T (n.382-51664G>T) c.289G>T (p.Gly97Trp) c.676G>T (p.Gly226Trp) c.673G>T (p.Gly225Trp) c.217G>T (p.Gly73Trp) | |
| 10 | g.113089521G>A | CA378532852 | TCF7L2 | c.483+49395G>A (n.483+49395G>A) c.552+49395G>A (n.552+49395G>A) c.605G>A (p.Gly202Glu) c.515G>A (p.Gly172Glu) c.608G>A (p.Gly203Glu) c.382-51663G>A (n.382-51663G>A) c.290G>A (p.Gly97Glu) c.677G>A (p.Gly226Glu) c.674G>A (p.Gly225Glu) c.218G>A (p.Gly73Glu) | |
| 10 | g.113089521G>C | CA378532851 | TCF7L2 | c.483+49395G>C (n.483+49395G>C) c.552+49395G>C (n.552+49395G>C) c.605G>C (p.Gly202Ala) c.515G>C (p.Gly172Ala) c.608G>C (p.Gly203Ala) c.382-51663G>C (n.382-51663G>C) c.290G>C (p.Gly97Ala) c.677G>C (p.Gly226Ala) c.674G>C (p.Gly225Ala) c.218G>C (p.Gly73Ala) | |
| 10 | g.113089521G>T | CA378532850 | TCF7L2 | c.483+49395G>T (n.483+49395G>T) c.552+49395G>T (n.552+49395G>T) c.605G>T (p.Gly202Val) c.515G>T (p.Gly172Val) c.608G>T (p.Gly203Val) c.382-51663G>T (n.382-51663G>T) c.290G>T (p.Gly97Val) c.677G>T (p.Gly226Val) c.674G>T (p.Gly225Val) c.218G>T (p.Gly73Val) | |
| 10 | g.113089523G>A | CA214116536 | TCF7L2 | c.483+49397G>A (n.483+49397G>A) c.552+49397G>A (n.552+49397G>A) c.607G>A (p.Glu203Lys) c.517G>A (p.Glu173Lys) c.610G>A (p.Glu204Lys) c.382-51661G>A (n.382-51661G>A) c.292G>A (p.Glu98Lys) c.679G>A (p.Glu227Lys) c.676G>A (p.Glu226Lys) c.220G>A (p.Glu74Lys) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.113089523G>C | CA378532853 | TCF7L2 | c.483+49397G>C (n.483+49397G>C) c.552+49397G>C (n.552+49397G>C) c.607G>C (p.Glu203Gln) c.517G>C (p.Glu173Gln) c.610G>C (p.Glu204Gln) c.382-51661G>C (n.382-51661G>C) c.292G>C (p.Glu98Gln) c.679G>C (p.Glu227Gln) c.676G>C (p.Glu226Gln) c.220G>C (p.Glu74Gln) | |
| 10 | g.113089523G= | CA1937197480 | TCF7L2 | c.483+49397G= (n.483+49397G=) c.552+49397G= (n.552+49397G=) c.607G= (p.Glu203=) c.517G= (p.Glu173=) c.610G= (p.Glu204=) c.382-51661G= (n.382-51661G=) c.292G= (p.Glu98=) c.679G= (p.Glu227=) c.676G= (p.Glu226=) c.220G= (p.Glu74=) | |
| 10 | g.113089523G>T | CA378532854 | TCF7L2 | c.483+49397G>T (n.483+49397G>T) c.552+49397G>T (n.552+49397G>T) c.607G>T (p.Glu203Ter) c.517G>T (p.Glu173Ter) c.610G>T (p.Glu204Ter) c.382-51661G>T (n.382-51661G>T) c.292G>T (p.Glu98Ter) c.679G>T (p.Glu227Ter) c.676G>T (p.Glu226Ter) c.220G>T (p.Glu74Ter) | |
| 10 | g.113089524A>C | CA378532855 | TCF7L2 | c.483+49398A>C (n.483+49398A>C) c.552+49398A>C (n.552+49398A>C) c.608A>C (p.Glu203Ala) c.518A>C (p.Glu173Ala) c.611A>C (p.Glu204Ala) c.382-51660A>C (n.382-51660A>C) c.293A>C (p.Glu98Ala) c.680A>C (p.Glu227Ala) c.677A>C (p.Glu226Ala) c.221A>C (p.Glu74Ala) | |
| 10 | g.113089524A>G | CA378532856 | TCF7L2 | c.483+49398A>G (n.483+49398A>G) c.552+49398A>G (n.552+49398A>G) c.608A>G (p.Glu203Gly) c.518A>G (p.Glu173Gly) c.611A>G (p.Glu204Gly) c.382-51660A>G (n.382-51660A>G) c.293A>G (p.Glu98Gly) c.680A>G (p.Glu227Gly) c.677A>G (p.Glu226Gly) c.221A>G (p.Glu74Gly) | |
| 10 | g.113089524A>T | CA378532857 | TCF7L2 | c.483+49398A>T (n.483+49398A>T) c.552+49398A>T (n.552+49398A>T) c.608A>T (p.Glu203Val) c.518A>T (p.Glu173Val) c.611A>T (p.Glu204Val) c.382-51660A>T (n.382-51660A>T) c.293A>T (p.Glu98Val) c.680A>T (p.Glu227Val) c.677A>T (p.Glu226Val) c.221A>T (p.Glu74Val) | |
| 10 | g.113089525G>A | CA5692914 | TCF7L2 | c.483+49399G>A (n.483+49399G>A) c.552+49399G>A (n.552+49399G>A) c.609G>A (p.Glu203=) c.519G>A (p.Glu173=) c.612G>A (p.Glu204=) c.382-51659G>A (n.382-51659G>A) c.294G>A (p.Glu98=) c.681G>A (p.Glu227=) c.678G>A (p.Glu226=) c.222G>A (p.Glu74=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.113089525G>C | CA378532859 | TCF7L2 | c.483+49399G>C (n.483+49399G>C) c.552+49399G>C (n.552+49399G>C) c.609G>C (p.Glu203Asp) c.519G>C (p.Glu173Asp) c.612G>C (p.Glu204Asp) c.382-51659G>C (n.382-51659G>C) c.294G>C (p.Glu98Asp) c.681G>C (p.Glu227Asp) c.678G>C (p.Glu226Asp) c.222G>C (p.Glu74Asp) | |
| 10 | g.113089525G= | CA1937197481 | TCF7L2 | c.483+49399G= (n.483+49399G=) c.552+49399G= (n.552+49399G=) c.609G= (p.Glu203=) c.519G= (p.Glu173=) c.612G= (p.Glu204=) c.382-51659G= (n.382-51659G=) c.294G= (p.Glu98=) c.681G= (p.Glu227=) c.678G= (p.Glu226=) c.222G= (p.Glu74=) | |
| 10 | g.113089525G>T | CA378532858 | TCF7L2 | c.483+49399G>T (n.483+49399G>T) c.552+49399G>T (n.552+49399G>T) c.609G>T (p.Glu203Asp) c.519G>T (p.Glu173Asp) c.612G>T (p.Glu204Asp) c.382-51659G>T (n.382-51659G>T) c.294G>T (p.Glu98Asp) c.681G>T (p.Glu227Asp) c.678G>T (p.Glu226Asp) c.222G>T (p.Glu74Asp) | |
| 10 | g.113089526C>A | CA378532860 | TCF7L2 | c.483+49400C>A (n.483+49400C>A) c.552+49400C>A (n.552+49400C>A) c.610C>A (p.Pro204Thr) c.520C>A (p.Pro174Thr) c.613C>A (p.Pro205Thr) c.382-51658C>A (n.382-51658C>A) c.295C>A (p.Pro99Thr) c.682C>A (p.Pro228Thr) c.679C>A (p.Pro227Thr) c.223C>A (p.Pro75Thr) | |
| 10 | g.113089526C= | CA1937197482 | TCF7L2 | c.483+49400C= (n.483+49400C=) c.552+49400C= (n.552+49400C=) c.610C= (p.Pro204=) c.520C= (p.Pro174=) c.613C= (p.Pro205=) c.382-51658C= (n.382-51658C=) c.295C= (p.Pro99=) c.682C= (p.Pro228=) c.679C= (p.Pro227=) c.223C= (p.Pro75=) | |
| 10 | g.113089526C>G | CA378532861 | TCF7L2 | c.483+49400C>G (n.483+49400C>G) c.552+49400C>G (n.552+49400C>G) c.610C>G (p.Pro204Ala) c.520C>G (p.Pro174Ala) c.613C>G (p.Pro205Ala) c.382-51658C>G (n.382-51658C>G) c.295C>G (p.Pro99Ala) c.682C>G (p.Pro228Ala) c.679C>G (p.Pro227Ala) c.223C>G (p.Pro75Ala) | |
| 10 | g.113089526C>T | CA378532862 | TCF7L2 | c.483+49400C>T (n.483+49400C>T) c.552+49400C>T (n.552+49400C>T) c.610C>T (p.Pro204Ser) c.520C>T (p.Pro174Ser) c.613C>T (p.Pro205Ser) c.382-51658C>T (n.382-51658C>T) c.295C>T (p.Pro99Ser) c.682C>T (p.Pro228Ser) c.679C>T (p.Pro227Ser) c.223C>T (p.Pro75Ser) | dbSNP gnomAD v4 |
| 10 | g.113089527C>A | CA378532863 | TCF7L2 | c.483+49401C>A (n.483+49401C>A) c.552+49401C>A (n.552+49401C>A) c.611C>A (p.Pro204His) c.521C>A (p.Pro174His) c.614C>A (p.Pro205His) c.382-51657C>A (n.382-51657C>A) c.296C>A (p.Pro99His) c.683C>A (p.Pro228His) c.680C>A (p.Pro227His) c.224C>A (p.Pro75His) | |
| 10 | g.113089527C= | CA1937197483 | TCF7L2 | c.483+49401C= (n.483+49401C=) c.552+49401C= (n.552+49401C=) c.611C= (p.Pro204=) c.521C= (p.Pro174=) c.614C= (p.Pro205=) c.382-51657C= (n.382-51657C=) c.296C= (p.Pro99=) c.683C= (p.Pro228=) c.680C= (p.Pro227=) c.224C= (p.Pro75=) | |
| 10 | g.113089527C>G | CA378532864 | TCF7L2 | c.483+49401C>G (n.483+49401C>G) c.552+49401C>G (n.552+49401C>G) c.611C>G (p.Pro204Arg) c.521C>G (p.Pro174Arg) c.614C>G (p.Pro205Arg) c.382-51657C>G (n.382-51657C>G) c.296C>G (p.Pro99Arg) c.683C>G (p.Pro228Arg) c.680C>G (p.Pro227Arg) c.224C>G (p.Pro75Arg) | |
| 10 | g.113089527C>T | CA214116537 | TCF7L2 | c.483+49401C>T (n.483+49401C>T) c.552+49401C>T (n.552+49401C>T) c.611C>T (p.Pro204Leu) c.521C>T (p.Pro174Leu) c.614C>T (p.Pro205Leu) c.382-51657C>T (n.382-51657C>T) c.296C>T (p.Pro99Leu) c.683C>T (p.Pro228Leu) c.680C>T (p.Pro227Leu) c.224C>T (p.Pro75Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.113089529T>A | CA378532865 | TCF7L2 | c.483+49403T>A (n.483+49403T>A) c.552+49403T>A (n.552+49403T>A) c.613T>A (p.Trp205Arg) c.523T>A (p.Trp175Arg) c.616T>A (p.Trp206Arg) c.382-51655T>A (n.382-51655T>A) c.298T>A (p.Trp100Arg) c.685T>A (p.Trp229Arg) c.682T>A (p.Trp228Arg) c.226T>A (p.Trp76Arg) | |
| 10 | g.113089529T>C | CA378532866 | TCF7L2 | c.483+49403T>C (n.483+49403T>C) c.552+49403T>C (n.552+49403T>C) c.613T>C (p.Trp205Arg) c.523T>C (p.Trp175Arg) c.616T>C (p.Trp206Arg) c.382-51655T>C (n.382-51655T>C) c.298T>C (p.Trp100Arg) c.685T>C (p.Trp229Arg) c.682T>C (p.Trp228Arg) c.226T>C (p.Trp76Arg) | |
| 10 | g.113089529T>G | CA378532867 | TCF7L2 | c.483+49403T>G (n.483+49403T>G) c.552+49403T>G (n.552+49403T>G) c.613T>G (p.Trp205Gly) c.523T>G (p.Trp175Gly) c.616T>G (p.Trp206Gly) c.382-51655T>G (n.382-51655T>G) c.298T>G (p.Trp100Gly) c.685T>G (p.Trp229Gly) c.682T>G (p.Trp228Gly) c.226T>G (p.Trp76Gly) | |
| 10 | g.113089530G>A | CA378532868 | TCF7L2 | c.483+49404G>A (n.483+49404G>A) c.552+49404G>A (n.552+49404G>A) c.614G>A (p.Trp205Ter) c.524G>A (p.Trp175Ter) c.617G>A (p.Trp206Ter) c.382-51654G>A (n.382-51654G>A) c.299G>A (p.Trp100Ter) c.686G>A (p.Trp229Ter) c.683G>A (p.Trp228Ter) c.227G>A (p.Trp76Ter) | |
| 10 | g.113089530G>C | CA378532869 | TCF7L2 | c.483+49404G>C (n.483+49404G>C) c.552+49404G>C (n.552+49404G>C) c.614G>C (p.Trp205Ser) c.524G>C (p.Trp175Ser) c.617G>C (p.Trp206Ser) c.382-51654G>C (n.382-51654G>C) c.299G>C (p.Trp100Ser) c.686G>C (p.Trp229Ser) c.683G>C (p.Trp228Ser) c.227G>C (p.Trp76Ser) | |
| 10 | g.113089530G= | CA1937197484 | TCF7L2 | c.483+49404G= (n.483+49404G=) c.552+49404G= (n.552+49404G=) c.614G= (p.Trp205=) c.524G= (p.Trp175=) c.617G= (p.Trp206=) c.382-51654G= (n.382-51654G=) c.299G= (p.Trp100=) c.686G= (p.Trp229=) c.683G= (p.Trp228=) c.227G= (p.Trp76=) | |
| 10 | g.113089530G>T | CA378532870 | TCF7L2 | c.483+49404G>T (n.483+49404G>T) c.552+49404G>T (n.552+49404G>T) c.614G>T (p.Trp205Leu) c.524G>T (p.Trp175Leu) c.617G>T (p.Trp206Leu) c.382-51654G>T (n.382-51654G>T) c.299G>T (p.Trp100Leu) c.686G>T (p.Trp229Leu) c.683G>T (p.Trp228Leu) c.227G>T (p.Trp76Leu) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.113089531G>A | CA378532872 | TCF7L2 | c.483+49405G>A (n.483+49405G>A) c.552+49405G>A (n.552+49405G>A) c.615G>A (p.Trp205Ter) c.525G>A (p.Trp175Ter) c.618G>A (p.Trp206Ter) c.382-51653G>A (n.382-51653G>A) c.300G>A (p.Trp100Ter) c.687G>A (p.Trp229Ter) c.684G>A (p.Trp228Ter) c.228G>A (p.Trp76Ter) | |
| 10 | g.113089531G>C | CA378532873 | TCF7L2 | c.483+49405G>C (n.483+49405G>C) c.552+49405G>C (n.552+49405G>C) c.615G>C (p.Trp205Cys) c.525G>C (p.Trp175Cys) c.618G>C (p.Trp206Cys) c.382-51653G>C (n.382-51653G>C) c.300G>C (p.Trp100Cys) c.687G>C (p.Trp229Cys) c.684G>C (p.Trp228Cys) c.228G>C (p.Trp76Cys) | dbSNP gnomAD v3 gnomAD v4 |
| 10 | g.113089531G= | CA1937197485 | TCF7L2 | c.483+49405G= (n.483+49405G=) c.552+49405G= (n.552+49405G=) c.615G= (p.Trp205=) c.525G= (p.Trp175=) c.618G= (p.Trp206=) c.382-51653G= (n.382-51653G=) c.300G= (p.Trp100=) c.687G= (p.Trp229=) c.684G= (p.Trp228=) c.228G= (p.Trp76=) | |
| 10 | g.113089531G>T | CA378532871 | TCF7L2 | c.483+49405G>T (n.483+49405G>T) c.552+49405G>T (n.552+49405G>T) c.615G>T (p.Trp205Cys) c.525G>T (p.Trp175Cys) c.618G>T (p.Trp206Cys) c.382-51653G>T (n.382-51653G>T) c.300G>T (p.Trp100Cys) c.687G>T (p.Trp229Cys) c.684G>T (p.Trp228Cys) c.228G>T (p.Trp76Cys) | |
| 10 | g.113089532T>A | CA378532874 | TCF7L2 | c.483+49406T>A (n.483+49406T>A) c.552+49406T>A (n.552+49406T>A) c.616T>A (p.Cys206Ser) c.526T>A (p.Cys176Ser) c.619T>A (p.Cys207Ser) c.382-51652T>A (n.382-51652T>A) c.301T>A (p.Cys101Ser) c.688T>A (p.Cys230Ser) c.685T>A (p.Cys229Ser) c.229T>A (p.Cys77Ser) | |
| 10 | g.113089532T>C | CA378532876 | TCF7L2 | c.483+49406T>C (n.483+49406T>C) c.552+49406T>C (n.552+49406T>C) c.616T>C (p.Cys206Arg) c.526T>C (p.Cys176Arg) c.619T>C (p.Cys207Arg) c.382-51652T>C (n.382-51652T>C) c.301T>C (p.Cys101Arg) c.688T>C (p.Cys230Arg) c.685T>C (p.Cys229Arg) c.229T>C (p.Cys77Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.113089532T>G | CA378532875 | TCF7L2 | c.483+49406T>G (n.483+49406T>G) c.552+49406T>G (n.552+49406T>G) c.616T>G (p.Cys206Gly) c.526T>G (p.Cys176Gly) c.619T>G (p.Cys207Gly) c.382-51652T>G (n.382-51652T>G) c.301T>G (p.Cys101Gly) c.688T>G (p.Cys230Gly) c.685T>G (p.Cys229Gly) c.229T>G (p.Cys77Gly) | |
| 10 | g.113089532T= | CA1937197486 | TCF7L2 | c.483+49406T= (n.483+49406T=) c.552+49406T= (n.552+49406T=) c.616T= (p.Cys206=) c.526T= (p.Cys176=) c.619T= (p.Cys207=) c.382-51652T= (n.382-51652T=) c.301T= (p.Cys101=) c.688T= (p.Cys230=) c.685T= (p.Cys229=) c.229T= (p.Cys77=) | |
| 10 | g.113089533G>A | CA5692915 | TCF7L2 | c.483+49407G>A (n.483+49407G>A) c.552+49407G>A (n.552+49407G>A) c.617G>A (p.Cys206Tyr) c.527G>A (p.Cys176Tyr) c.620G>A (p.Cys207Tyr) c.382-51651G>A (n.382-51651G>A) c.302G>A (p.Cys101Tyr) c.689G>A (p.Cys230Tyr) c.686G>A (p.Cys229Tyr) c.230G>A (p.Cys77Tyr) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 10 | g.113089533G>C | CA378532877 | TCF7L2 | c.483+49407G>C (n.483+49407G>C) c.552+49407G>C (n.552+49407G>C) c.617G>C (p.Cys206Ser) c.527G>C (p.Cys176Ser) c.620G>C (p.Cys207Ser) c.382-51651G>C (n.382-51651G>C) c.302G>C (p.Cys101Ser) c.689G>C (p.Cys230Ser) c.686G>C (p.Cys229Ser) c.230G>C (p.Cys77Ser) | |
| 10 | g.113089533G= | CA1937197487 | TCF7L2 | c.483+49407G= (n.483+49407G=) c.552+49407G= (n.552+49407G=) c.617G= (p.Cys206=) c.527G= (p.Cys176=) c.620G= (p.Cys207=) c.382-51651G= (n.382-51651G=) c.302G= (p.Cys101=) c.689G= (p.Cys230=) c.686G= (p.Cys229=) c.230G= (p.Cys77=) |