Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.30672085A=CA1354873117TGFBR2c.902A= (p.His301=)
n.2498A=
c.977A= (p.His326=)
c.929A= (p.His310=)
c.854A= (p.His285=)
c.797A= (p.His266=)
3g.30672085A>CCA351808129TGFBR2c.902A>C (p.His301Pro)
n.2498A>C
c.977A>C (p.His326Pro)
c.929A>C (p.His310Pro)
c.854A>C (p.His285Pro)
c.797A>C (p.His266Pro)
3g.30672085A>GCA325027TGFBR2c.902A>G (p.His301Arg)
n.2498A>G
c.977A>G (p.His326Arg)
c.929A>G (p.His310Arg)
c.854A>G (p.His285Arg)
c.797A>G (p.His266Arg)
 ClinVar dbSNP gnomAD v4
3g.30672085A>TCA351808130TGFBR2c.902A>T (p.His301Leu)
n.2498A>T
c.977A>T (p.His326Leu)
c.929A>T (p.His310Leu)
c.854A>T (p.His285Leu)
c.797A>T (p.His266Leu)
3g.30672086T>ACA351808131TGFBR2c.903T>A (p.His301Gln)
n.2499T>A
c.978T>A (p.His326Gln)
c.930T>A (p.His310Gln)
c.855T>A (p.His285Gln)
c.798T>A (p.His266Gln)
 dbSNP
3g.30672086T>CCA433058883TGFBR2c.903T>C (p.His301=)
n.2499T>C
c.978T>C (p.His326=)
c.930T>C (p.His310=)
c.855T>C (p.His285=)
c.798T>C (p.His266=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672086T>GCA351808132TGFBR2c.903T>G (p.His301Gln)
n.2499T>G
c.978T>G (p.His326Gln)
c.930T>G (p.His310Gln)
c.855T>G (p.His285Gln)
c.798T>G (p.His266Gln)
3g.30672086T=CA1354873118TGFBR2c.903T= (p.His301=)
n.2499T=
c.978T= (p.His326=)
c.930T= (p.His310=)
c.855T= (p.His285=)
c.798T= (p.His266=)
3g.30672087G>ACA351808134TGFBR2c.904G>A (p.Glu302Lys)
n.2500G>A
c.979G>A (p.Glu327Lys)
c.931G>A (p.Glu311Lys)
c.856G>A (p.Glu286Lys)
c.799G>A (p.Glu267Lys)
 ClinVar dbSNP gnomAD v4
3g.30672087G>CCA351808135TGFBR2c.904G>C (p.Glu302Gln)
n.2500G>C
c.979G>C (p.Glu327Gln)
c.931G>C (p.Glu311Gln)
c.856G>C (p.Glu286Gln)
c.799G>C (p.Glu267Gln)
 dbSNP
3g.30672087G>TCA351808133TGFBR2c.904G>T (p.Glu302Ter)
n.2500G>T
c.979G>T (p.Glu327Ter)
c.931G>T (p.Glu311Ter)
c.856G>T (p.Glu286Ter)
c.799G>T (p.Glu267Ter)
 COSMIC COSMIC
3g.30672088A=CA1354873119TGFBR2c.905A= (p.Glu302=)
n.2501A=
c.980A= (p.Glu327=)
c.932A= (p.Glu311=)
c.857A= (p.Glu286=)
c.800A= (p.Glu267=)
3g.30672088A>CCA351808136TGFBR2c.905A>C (p.Glu302Ala)
n.2501A>C
c.980A>C (p.Glu327Ala)
c.932A>C (p.Glu311Ala)
c.857A>C (p.Glu286Ala)
c.800A>C (p.Glu267Ala)
3g.30672088A>GCA351808137TGFBR2c.905A>G (p.Glu302Gly)
n.2501A>G
c.980A>G (p.Glu327Gly)
c.932A>G (p.Glu311Gly)
c.857A>G (p.Glu286Gly)
c.800A>G (p.Glu267Gly)
3g.30672088A>TCA050112TGFBR2c.905A>T (p.Glu302Val)
n.2501A>T
c.980A>T (p.Glu327Val)
c.932A>T (p.Glu311Val)
c.857A>T (p.Glu286Val)
c.800A>T (p.Glu267Val)
 dbSNP ExAC gnomAD v2
3g.30672089G>ACA71528263TGFBR2c.906G>A (p.Glu302=)
n.2502G>A
c.981G>A (p.Glu327=)
c.933G>A (p.Glu311=)
c.858G>A (p.Glu286=)
c.801G>A (p.Glu267=)
 ClinVar dbSNP gnomAD v4
3g.30672089G>CCA351808138TGFBR2c.906G>C (p.Glu302Asp)
n.2502G>C
c.981G>C (p.Glu327Asp)
c.933G>C (p.Glu311Asp)
c.858G>C (p.Glu286Asp)
c.801G>C (p.Glu267Asp)
 dbSNP
3g.30672089G=CA1354873120TGFBR2c.906G= (p.Glu302=)
n.2502G=
c.981G= (p.Glu327=)
c.933G= (p.Glu311=)
c.858G= (p.Glu286=)
c.801G= (p.Glu267=)
3g.30672089G>TCA351808139TGFBR2c.906G>T (p.Glu302Asp)
n.2502G>T
c.981G>T (p.Glu327Asp)
c.933G>T (p.Glu311Asp)
c.858G>T (p.Glu286Asp)
c.801G>T (p.Glu267Asp)
 dbSNP
3g.30672090A=CA1354873121TGFBR2c.907A= (p.Asn303=)
n.2503A=
c.982A= (p.Asn328=)
c.934A= (p.Asn312=)
c.859A= (p.Asn287=)
c.802A= (p.Asn268=)
3g.30672090A>CCA050124TGFBR2c.907A>C (p.Asn303His)
n.2503A>C
c.982A>C (p.Asn328His)
c.934A>C (p.Asn312His)
c.859A>C (p.Asn287His)
c.802A>C (p.Asn268His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672090A>GCA351808140TGFBR2c.907A>G (p.Asn303Asp)
n.2503A>G
c.982A>G (p.Asn328Asp)
c.934A>G (p.Asn312Asp)
c.859A>G (p.Asn287Asp)
c.802A>G (p.Asn268Asp)
3g.30672090A>TCA351808141TGFBR2c.907A>T (p.Asn303Tyr)
n.2503A>T
c.982A>T (p.Asn328Tyr)
c.934A>T (p.Asn312Tyr)
c.859A>T (p.Asn287Tyr)
c.802A>T (p.Asn268Tyr)
 dbSNP
3g.30672091dupCA2664867668TGFBR2c.908dup (p.Asn303LysfsTer9)
n.2504dup
c.983dup (p.Asn328LysfsTer9)
c.935dup (p.Asn312LysfsTer9)
c.860dup (p.Asn287LysfsTer9)
c.803dup (p.Asn268LysfsTer9)
 gnomAD v4
3g.30672091A>CCA351808142TGFBR2c.908A>C (p.Asn303Thr)
n.2504A>C
c.983A>C (p.Asn328Thr)
c.935A>C (p.Asn312Thr)
c.860A>C (p.Asn287Thr)
c.803A>C (p.Asn268Thr)
3g.30672091A>GCA351808143TGFBR2c.908A>G (p.Asn303Ser)
n.2504A>G
c.983A>G (p.Asn328Ser)
c.935A>G (p.Asn312Ser)
c.860A>G (p.Asn287Ser)
c.803A>G (p.Asn268Ser)
 ClinVar dbSNP
3g.30672091A>TCA351808144TGFBR2c.908A>T (p.Asn303Ile)
n.2504A>T
c.983A>T (p.Asn328Ile)
c.935A>T (p.Asn312Ile)
c.860A>T (p.Asn287Ile)
c.803A>T (p.Asn268Ile)
 dbSNP
3g.30672092C>ACA351808145TGFBR2c.909C>A (p.Asn303Lys)
n.2505C>A
c.984C>A (p.Asn328Lys)
c.936C>A (p.Asn312Lys)
c.861C>A (p.Asn287Lys)
c.804C>A (p.Asn268Lys)
 dbSNP gnomAD v4
3g.30672092C>GCA351808146TGFBR2c.909C>G (p.Asn303Lys)
n.2505C>G
c.984C>G (p.Asn328Lys)
c.936C>G (p.Asn312Lys)
c.861C>G (p.Asn287Lys)
c.804C>G (p.Asn268Lys)
 dbSNP
3g.30672092C>TCA433058885TGFBR2c.909C>T (p.Asn303=)
n.2505C>T
c.984C>T (p.Asn328=)
c.936C>T (p.Asn312=)
c.861C>T (p.Asn287=)
c.804C>T (p.Asn268=)
 dbSNP gnomAD v4
3g.30672093A=CA1354873122TGFBR2c.910A= (p.Ile304=)
n.2506A=
c.985A= (p.Ile329=)
c.937A= (p.Ile313=)
c.862A= (p.Ile288=)
c.805A= (p.Ile269=)
3g.30672093A>CCA351808149TGFBR2c.910A>C (p.Ile304Leu)
n.2506A>C
c.985A>C (p.Ile329Leu)
c.937A>C (p.Ile313Leu)
c.862A>C (p.Ile288Leu)
c.805A>C (p.Ile269Leu)
3g.30672093A>GCA351808148TGFBR2c.910A>G (p.Ile304Val)
n.2506A>G
c.985A>G (p.Ile329Val)
c.937A>G (p.Ile313Val)
c.862A>G (p.Ile288Val)
c.805A>G (p.Ile269Val)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672093A>TCA351808147TGFBR2c.910A>T (p.Ile304Leu)
n.2506A>T
c.985A>T (p.Ile329Leu)
c.937A>T (p.Ile313Leu)
c.862A>T (p.Ile288Leu)
c.805A>T (p.Ile269Leu)
 dbSNP gnomAD v4
3g.30672094T>ACA351808150TGFBR2c.911T>A (p.Ile304Lys)
n.2507T>A
c.986T>A (p.Ile329Lys)
c.938T>A (p.Ile313Lys)
c.863T>A (p.Ile288Lys)
c.806T>A (p.Ile269Lys)
 dbSNP
3g.30672094T>CCA351808151TGFBR2c.911T>C (p.Ile304Thr)
n.2507T>C
c.986T>C (p.Ile329Thr)
c.938T>C (p.Ile313Thr)
c.863T>C (p.Ile288Thr)
c.806T>C (p.Ile269Thr)
 dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
3g.30672094T>GCA351808152TGFBR2c.911T>G (p.Ile304Arg)
n.2507T>G
c.986T>G (p.Ile329Arg)
c.938T>G (p.Ile313Arg)
c.863T>G (p.Ile288Arg)
c.806T>G (p.Ile269Arg)
 dbSNP
3g.30672094T=CA1354873123TGFBR2c.911T= (p.Ile304=)
n.2507T=
c.986T= (p.Ile329=)
c.938T= (p.Ile313=)
c.863T= (p.Ile288=)
c.806T= (p.Ile269=)
3g.30672095A=CA1354873124TGFBR2c.912A= (p.Ile304=)
n.2508A=
c.987A= (p.Ile329=)
c.939A= (p.Ile313=)
c.864A= (p.Ile288=)
c.807A= (p.Ile269=)
3g.30672095A>CCA433058890TGFBR2c.912A>C (p.Ile304=)
n.2508A>C
c.987A>C (p.Ile329=)
c.939A>C (p.Ile313=)
c.864A>C (p.Ile288=)
c.807A>C (p.Ile269=)
 dbSNP
3g.30672095A>GCA351808153TGFBR2c.912A>G (p.Ile304Met)
n.2508A>G
c.987A>G (p.Ile329Met)
c.939A>G (p.Ile313Met)
c.864A>G (p.Ile288Met)
c.807A>G (p.Ile269Met)
 ClinVar dbSNP
3g.30672095A>TCA433058889TGFBR2c.912A>T (p.Ile304=)
n.2508A>T
c.987A>T (p.Ile329=)
c.939A>T (p.Ile313=)
c.864A>T (p.Ile288=)
c.807A>T (p.Ile269=)
 dbSNP
3g.30672096C>ACA351808154TGFBR2c.913C>A (p.Leu305Ile)
n.2509C>A
c.988C>A (p.Leu330Ile)
c.940C>A (p.Leu314Ile)
c.865C>A (p.Leu289Ile)
c.808C>A (p.Leu270Ile)
 dbSNP
3g.30672096C=CA1354873125TGFBR2c.913C= (p.Leu305=)
n.2509C=
c.988C= (p.Leu330=)
c.940C= (p.Leu314=)
c.865C= (p.Leu289=)
c.808C= (p.Leu270=)
3g.30672096C>GCA351808155TGFBR2c.913C>G (p.Leu305Val)
n.2509C>G
c.988C>G (p.Leu330Val)
c.940C>G (p.Leu314Val)
c.865C>G (p.Leu289Val)
c.808C>G (p.Leu270Val)
 dbSNP
3g.30672096C>TCA351808156TGFBR2c.913C>T (p.Leu305Phe)
n.2509C>T
c.988C>T (p.Leu330Phe)
c.940C>T (p.Leu314Phe)
c.865C>T (p.Leu289Phe)
c.808C>T (p.Leu270Phe)
 ClinVar dbSNP
3g.30672097T>ACA351808157TGFBR2c.914T>A (p.Leu305His)
n.2510T>A
c.989T>A (p.Leu330His)
c.941T>A (p.Leu314His)
c.866T>A (p.Leu289His)
c.809T>A (p.Leu270His)
 ClinVar dbSNP
3g.30672097T>CCA351808158TGFBR2c.914T>C (p.Leu305Pro)
n.2510T>C
c.989T>C (p.Leu330Pro)
c.941T>C (p.Leu314Pro)
c.866T>C (p.Leu289Pro)
c.809T>C (p.Leu270Pro)
 ClinVar
3g.30672097T>GCA351808159TGFBR2c.914T>G (p.Leu305Arg)
n.2510T>G
c.989T>G (p.Leu330Arg)
c.941T>G (p.Leu314Arg)
c.866T>G (p.Leu289Arg)
c.809T>G (p.Leu270Arg)
 ClinVar dbSNP
3g.30672097T=CA1354873126TGFBR2c.914T= (p.Leu305=)
n.2510T=
c.989T= (p.Leu330=)
c.941T= (p.Leu314=)
c.866T= (p.Leu289=)
c.809T= (p.Leu270=)
3g.30672098C>ACA433058894TGFBR2c.915C>A (p.Leu305=)
n.2511C>A
c.990C>A (p.Leu330=)
c.942C>A (p.Leu314=)
c.867C>A (p.Leu289=)
c.810C>A (p.Leu270=)
 dbSNP
3g.30672098C=CA1354873127TGFBR2c.915C= (p.Leu305=)
n.2511C=
c.990C= (p.Leu330=)
c.942C= (p.Leu314=)
c.867C= (p.Leu289=)
c.810C= (p.Leu270=)
3g.30672098C>GCA050138TGFBR2c.915C>G (p.Leu305=)
n.2511C>G
c.990C>G (p.Leu330=)
c.942C>G (p.Leu314=)
c.867C>G (p.Leu289=)
c.810C>G (p.Leu270=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672098C>TCA050149TGFBR2c.915C>T (p.Leu305=)
n.2511C>T
c.990C>T (p.Leu330=)
c.942C>T (p.Leu314=)
c.867C>T (p.Leu289=)
c.810C>T (p.Leu270=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672098_30672099delinsTCATGCA2586965651TGFBR2c.915_916delinsTCATG (p.Gln306delinsHisGlu)
n.2511_2512delinsTCATG
c.990_991delinsTCATG (p.Gln331delinsHisGlu)
c.942_943delinsTCATG (p.Gln315delinsHisGlu)
c.867_868delinsTCATG (p.Gln290delinsHisGlu)
c.810_811delinsTCATG (p.Gln271delinsHisGlu)
3g.30672099C>ACA351808162TGFBR2c.916C>A (p.Gln306Lys)
n.2512C>A
c.991C>A (p.Gln331Lys)
c.943C>A (p.Gln315Lys)
c.868C>A (p.Gln290Lys)
c.811C>A (p.Gln271Lys)
 dbSNP
3g.30672099C>GCA351808161TGFBR2c.916C>G (p.Gln306Glu)
n.2512C>G
c.991C>G (p.Gln331Glu)
c.943C>G (p.Gln315Glu)
c.868C>G (p.Gln290Glu)
c.811C>G (p.Gln271Glu)
 dbSNP
3g.30672099C>TCA351808160TGFBR2c.916C>T (p.Gln306Ter)
n.2512C>T
c.991C>T (p.Gln331Ter)
c.943C>T (p.Gln315Ter)
c.868C>T (p.Gln290Ter)
c.811C>T (p.Gln271Ter)
 dbSNP gnomAD v4 COSMIC
3g.30672100A>CCA351808163TGFBR2c.917A>C (p.Gln306Pro)
n.2513A>C
c.992A>C (p.Gln331Pro)
c.944A>C (p.Gln315Pro)
c.869A>C (p.Gln290Pro)
c.812A>C (p.Gln271Pro)
3g.30672100A>GCA351808165TGFBR2c.917A>G (p.Gln306Arg)
n.2513A>G
c.992A>G (p.Gln331Arg)
c.944A>G (p.Gln315Arg)
c.869A>G (p.Gln290Arg)
c.812A>G (p.Gln271Arg)
3g.30672100A>TCA351808164TGFBR2c.917A>T (p.Gln306Leu)
n.2513A>T
c.992A>T (p.Gln331Leu)
c.944A>T (p.Gln315Leu)
c.869A>T (p.Gln290Leu)
c.812A>T (p.Gln271Leu)
 dbSNP
3g.30672101G>ACA433058895TGFBR2c.918G>A (p.Gln306=)
n.2514G>A
c.993G>A (p.Gln331=)
c.945G>A (p.Gln315=)
c.870G>A (p.Gln290=)
c.813G>A (p.Gln271=)
 dbSNP
3g.30672101G>CCA351808166TGFBR2c.918G>C (p.Gln306His)
n.2514G>C
c.993G>C (p.Gln331His)
c.945G>C (p.Gln315His)
c.870G>C (p.Gln290His)
c.813G>C (p.Gln271His)
 dbSNP gnomAD v2 gnomAD v4
3g.30672101G=CA1354873128TGFBR2c.918G= (p.Gln306=)
n.2514G=
c.993G= (p.Gln331=)
c.945G= (p.Gln315=)
c.870G= (p.Gln290=)
c.813G= (p.Gln271=)
3g.30672101G>TCA351808167TGFBR2c.918G>T (p.Gln306His)
n.2514G>T
c.993G>T (p.Gln331His)
c.945G>T (p.Gln315His)
c.870G>T (p.Gln290His)
c.813G>T (p.Gln271His)
3g.30672102T>ACA351808168TGFBR2c.919T>A (p.Phe307Ile)
n.2515T>A
c.994T>A (p.Phe332Ile)
c.946T>A (p.Phe316Ile)
c.871T>A (p.Phe291Ile)
c.814T>A (p.Phe272Ile)
 dbSNP
3g.30672102T>CCA351808169TGFBR2c.919T>C (p.Phe307Leu)
n.2515T>C
c.994T>C (p.Phe332Leu)
c.946T>C (p.Phe316Leu)
c.871T>C (p.Phe291Leu)
c.814T>C (p.Phe272Leu)
 dbSNP
3g.30672102T>GCA351808170TGFBR2c.919T>G (p.Phe307Val)
n.2515T>G
c.994T>G (p.Phe332Val)
c.946T>G (p.Phe316Val)
c.871T>G (p.Phe291Val)
c.814T>G (p.Phe272Val)
 dbSNP
3g.30672103T>ACA351808171TGFBR2c.920T>A (p.Phe307Tyr)
n.2516T>A
c.995T>A (p.Phe332Tyr)
c.947T>A (p.Phe316Tyr)
c.872T>A (p.Phe291Tyr)
c.815T>A (p.Phe272Tyr)
 dbSNP
3g.30672103T>CCA351808172TGFBR2c.920T>C (p.Phe307Ser)
n.2516T>C
c.995T>C (p.Phe332Ser)
c.947T>C (p.Phe316Ser)
c.872T>C (p.Phe291Ser)
c.815T>C (p.Phe272Ser)
 dbSNP
3g.30672103T>GCA351808173TGFBR2c.920T>G (p.Phe307Cys)
n.2516T>G
c.995T>G (p.Phe332Cys)
c.947T>G (p.Phe316Cys)
c.872T>G (p.Phe291Cys)
c.815T>G (p.Phe272Cys)
3g.30672104C>ACA351808174TGFBR2c.921C>A (p.Phe307Leu)
n.2517C>A
c.996C>A (p.Phe332Leu)
c.948C>A (p.Phe316Leu)
c.873C>A (p.Phe291Leu)
c.816C>A (p.Phe272Leu)
 gnomAD v4
3g.30672104C=CA1354873129TGFBR2c.921C= (p.Phe307=)
n.2517C=
c.996C= (p.Phe332=)
c.948C= (p.Phe316=)
c.873C= (p.Phe291=)
c.816C= (p.Phe272=)
3g.30672104C>GCA351808175TGFBR2c.921C>G (p.Phe307Leu)
n.2517C>G
c.996C>G (p.Phe332Leu)
c.948C>G (p.Phe316Leu)
c.873C>G (p.Phe291Leu)
c.816C>G (p.Phe272Leu)
 dbSNP
3g.30672104C>TCA71528298TGFBR2c.921C>T (p.Phe307=)
n.2517C>T
c.996C>T (p.Phe332=)
c.948C>T (p.Phe316=)
c.873C>T (p.Phe291=)
c.816C>T (p.Phe272=)
 dbSNP gnomAD v3 gnomAD v4
3g.30672105C>ACA351808176TGFBR2c.922C>A (p.Leu308Met)
n.2518C>A
c.997C>A (p.Leu333Met)
c.949C>A (p.Leu317Met)
c.874C>A (p.Leu292Met)
c.817C>A (p.Leu273Met)
3g.30672105C>GCA351808177TGFBR2c.922C>G (p.Leu308Val)
n.2518C>G
c.997C>G (p.Leu333Val)
c.949C>G (p.Leu317Val)
c.874C>G (p.Leu292Val)
c.817C>G (p.Leu273Val)
 dbSNP
3g.30672105C>TCA433058897TGFBR2c.922C>T (p.Leu308=)
n.2518C>T
c.997C>T (p.Leu333=)
c.949C>T (p.Leu317=)
c.874C>T (p.Leu292=)
c.817C>T (p.Leu273=)
 dbSNP
3g.30672106T>ACA351808179TGFBR2c.923T>A (p.Leu308Gln)
n.2519T>A
c.998T>A (p.Leu333Gln)
c.950T>A (p.Leu317Gln)
c.875T>A (p.Leu292Gln)
c.818T>A (p.Leu273Gln)
3g.30672106T>CCA020791TGFBR2c.923T>C (p.Leu308Pro)
n.2519T>C
c.998T>C (p.Leu333Pro)
c.950T>C (p.Leu317Pro)
c.875T>C (p.Leu292Pro)
c.818T>C (p.Leu273Pro)
 ClinVar dbSNP
3g.30672106T>GCA351808178TGFBR2c.923T>G (p.Leu308Arg)
n.2519T>G
c.998T>G (p.Leu333Arg)
c.950T>G (p.Leu317Arg)
c.875T>G (p.Leu292Arg)
c.818T>G (p.Leu273Arg)
3g.30672106T=CA1354873130TGFBR2c.923T= (p.Leu308=)
n.2519T=
c.998T= (p.Leu333=)
c.950T= (p.Leu317=)
c.875T= (p.Leu292=)
c.818T= (p.Leu273=)
3g.30672107G>ACA433058898TGFBR2c.924G>A (p.Leu308=)
n.2520G>A
c.999G>A (p.Leu333=)
c.951G>A (p.Leu317=)
c.876G>A (p.Leu292=)
c.819G>A (p.Leu273=)
 ClinVar dbSNP
3g.30672107G>CCA433058900TGFBR2c.924G>C (p.Leu308=)
n.2520G>C
c.999G>C (p.Leu333=)
c.951G>C (p.Leu317=)
c.876G>C (p.Leu292=)
c.819G>C (p.Leu273=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672107G=CA1354873131TGFBR2c.924G= (p.Leu308=)
n.2520G=
c.999G= (p.Leu333=)
c.951G= (p.Leu317=)
c.876G= (p.Leu292=)
c.819G= (p.Leu273=)
3g.30672107G>TCA433058901TGFBR2c.924G>T (p.Leu308=)
n.2520G>T
c.999G>T (p.Leu333=)
c.951G>T (p.Leu317=)
c.876G>T (p.Leu292=)
c.819G>T (p.Leu273=)
 dbSNP gnomAD v4
3g.30672108A>CCA351808180TGFBR2c.925A>C (p.Thr309Pro)
n.2521A>C
c.1000A>C (p.Thr334Pro)
c.952A>C (p.Thr318Pro)
c.877A>C (p.Thr293Pro)
c.820A>C (p.Thr274Pro)
 dbSNP
3g.30672108A>GCA351808181TGFBR2c.925A>G (p.Thr309Ala)
n.2521A>G
c.1000A>G (p.Thr334Ala)
c.952A>G (p.Thr318Ala)
c.877A>G (p.Thr293Ala)
c.820A>G (p.Thr274Ala)
 dbSNP
3g.30672108A>TCA351808182TGFBR2c.925A>T (p.Thr309Ser)
n.2521A>T
c.1000A>T (p.Thr334Ser)
c.952A>T (p.Thr318Ser)
c.877A>T (p.Thr293Ser)
c.820A>T (p.Thr274Ser)
 dbSNP
3g.30672109C>ACA351808183TGFBR2c.926C>A (p.Thr309Lys)
n.2522C>A
c.1001C>A (p.Thr334Lys)
c.953C>A (p.Thr318Lys)
c.878C>A (p.Thr293Lys)
c.821C>A (p.Thr274Lys)
3g.30672109C=CA1354873132TGFBR2c.926C= (p.Thr309=)
n.2522C=
c.1001C= (p.Thr334=)
c.953C= (p.Thr318=)
c.878C= (p.Thr293=)
c.821C= (p.Thr274=)
3g.30672109C>GCA351808184TGFBR2c.926C>G (p.Thr309Arg)
n.2522C>G
c.1001C>G (p.Thr334Arg)
c.953C>G (p.Thr318Arg)
c.878C>G (p.Thr293Arg)
c.821C>G (p.Thr274Arg)
 dbSNP
3g.30672109C>TCA050182TGFBR2c.926C>T (p.Thr309Met)
n.2522C>T
c.1001C>T (p.Thr334Met)
c.953C>T (p.Thr318Met)
c.878C>T (p.Thr293Met)
c.821C>T (p.Thr274Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672110G>ACA050194TGFBR2c.927G>A (p.Thr309=)
n.2523G>A
c.1002G>A (p.Thr334=)
c.954G>A (p.Thr318=)
c.879G>A (p.Thr293=)
c.822G>A (p.Thr274=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.30672110G>CCA050207TGFBR2c.927G>C (p.Thr309=)
n.2523G>C
c.1002G>C (p.Thr334=)
c.954G>C (p.Thr318=)
c.879G>C (p.Thr293=)
c.822G>C (p.Thr274=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672110G=CA1354873133TGFBR2c.927G= (p.Thr309=)
n.2523G=
c.1002G= (p.Thr334=)
c.954G= (p.Thr318=)
c.879G= (p.Thr293=)
c.822G= (p.Thr274=)
3g.30672110G>TCA433058902TGFBR2c.927G>T (p.Thr309=)
n.2523G>T
c.1002G>T (p.Thr334=)
c.954G>T (p.Thr318=)
c.879G>T (p.Thr293=)
c.822G>T (p.Thr274=)
 dbSNP COSMIC COSMIC
3g.30672111G>ACA351808185TGFBR2c.928G>A (p.Ala310Thr)
n.2524G>A
c.1003G>A (p.Ala335Thr)
c.955G>A (p.Ala319Thr)
c.880G>A (p.Ala294Thr)
c.823G>A (p.Ala275Thr)
 ClinVar dbSNP gnomAD v4
3g.30672111G>CCA351808186TGFBR2c.928G>C (p.Ala310Pro)
n.2524G>C
c.1003G>C (p.Ala335Pro)
c.955G>C (p.Ala319Pro)
c.880G>C (p.Ala294Pro)
c.823G>C (p.Ala275Pro)
 dbSNP
3g.30672111G=CA1354873134TGFBR2c.928G= (p.Ala310=)
n.2524G=
c.1003G= (p.Ala335=)
c.955G= (p.Ala319=)
c.880G= (p.Ala294=)
c.823G= (p.Ala275=)
3g.30672111G>TCA351808187TGFBR2c.928G>T (p.Ala310Ser)
n.2524G>T
c.1003G>T (p.Ala335Ser)
c.955G>T (p.Ala319Ser)
c.880G>T (p.Ala294Ser)
c.823G>T (p.Ala275Ser)
 ClinVar dbSNP gnomAD v4
3g.30672112C>ACA351808190TGFBR2c.929C>A (p.Ala310Asp)
n.2525C>A
c.1004C>A (p.Ala335Asp)
c.956C>A (p.Ala319Asp)
c.881C>A (p.Ala294Asp)
c.824C>A (p.Ala275Asp)
 dbSNP
3g.30672112C>GCA351808189TGFBR2c.929C>G (p.Ala310Gly)
n.2525C>G
c.1004C>G (p.Ala335Gly)
c.956C>G (p.Ala319Gly)
c.881C>G (p.Ala294Gly)
c.824C>G (p.Ala275Gly)
 dbSNP gnomAD v4
3g.30672112C>TCA351808188TGFBR2c.929C>T (p.Ala310Val)
n.2525C>T
c.1004C>T (p.Ala335Val)
c.956C>T (p.Ala319Val)
c.881C>T (p.Ala294Val)
c.824C>T (p.Ala275Val)
 dbSNP
3g.30672113T>ACA433058906TGFBR2c.930T>A (p.Ala310=)
n.2526T>A
c.1005T>A (p.Ala335=)
c.957T>A (p.Ala319=)
c.882T>A (p.Ala294=)
c.825T>A (p.Ala275=)
 dbSNP
3g.30672113T>CCA433058907TGFBR2c.930T>C (p.Ala310=)
n.2526T>C
c.1005T>C (p.Ala335=)
c.957T>C (p.Ala319=)
c.882T>C (p.Ala294=)
c.825T>C (p.Ala275=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672113T>GCA433058908TGFBR2c.930T>G (p.Ala310=)
n.2526T>G
c.1005T>G (p.Ala335=)
c.957T>G (p.Ala319=)
c.882T>G (p.Ala294=)
c.825T>G (p.Ala275=)
 dbSNP
3g.30672113T=CA1354873135TGFBR2c.930T= (p.Ala310=)
n.2526T=
c.1005T= (p.Ala335=)
c.957T= (p.Ala319=)
c.882T= (p.Ala294=)
c.825T= (p.Ala275=)
3g.30672114G>ACA351808191TGFBR2c.931G>A (p.Glu311Lys)
n.2527G>A
c.1006G>A (p.Glu336Lys)
c.958G>A (p.Glu320Lys)
c.883G>A (p.Glu295Lys)
c.826G>A (p.Glu276Lys)
 dbSNP COSMIC COSMIC
3g.30672114G>CCA351808192TGFBR2c.931G>C (p.Glu311Gln)
n.2527G>C
c.1006G>C (p.Glu336Gln)
c.958G>C (p.Glu320Gln)
c.883G>C (p.Glu295Gln)
c.826G>C (p.Glu276Gln)
 dbSNP
3g.30672114G>TCA351808193TGFBR2c.931G>T (p.Glu311Ter)
n.2527G>T
c.1006G>T (p.Glu336Ter)
c.958G>T (p.Glu320Ter)
c.883G>T (p.Glu295Ter)
c.826G>T (p.Glu276Ter)
3g.30672115A>CCA351808194TGFBR2c.932A>C (p.Glu311Ala)
n.2528A>C
c.1007A>C (p.Glu336Ala)
c.959A>C (p.Glu320Ala)
c.884A>C (p.Glu295Ala)
c.827A>C (p.Glu276Ala)
3g.30672115A>GCA351808195TGFBR2c.932A>G (p.Glu311Gly)
n.2528A>G
c.1007A>G (p.Glu336Gly)
c.959A>G (p.Glu320Gly)
c.884A>G (p.Glu295Gly)
c.827A>G (p.Glu276Gly)
 dbSNP
3g.30672115A>TCA351808196TGFBR2c.932A>T (p.Glu311Val)
n.2528A>T
c.1007A>T (p.Glu336Val)
c.959A>T (p.Glu320Val)
c.884A>T (p.Glu295Val)
c.827A>T (p.Glu276Val)
 dbSNP
3g.30672115_30672135delinsAGGAGCGGAAGACGGAGTTGGCA1354873136TGFBR2c.932_952delinsAGGAGCGGAAGACGGAGTTGG (p.Glu311=)
n.2528_2548delinsAGGAGCGGAAGACGGAGTTGG
c.1007_1027delinsAGGAGCGGAAGACGGAGTTGG (p.Glu336=)
c.959_979delinsAGGAGCGGAAGACGGAGTTGG (p.Glu320=)
c.884_904delinsAGGAGCGGAAGACGGAGTTGG (p.Glu295=)
c.827_847delinsAGGAGCGGAAGACGGAGTTGG (p.Glu276=)
3g.30672116G>ACA050230TGFBR2c.933G>A (p.Glu311=)
n.2529G>A
c.1008G>A (p.Glu336=)
c.960G>A (p.Glu320=)
c.885G>A (p.Glu295=)
c.828G>A (p.Glu276=)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
3g.30672116G>CCA351808197TGFBR2c.933G>C (p.Glu311Asp)
n.2529G>C
c.1008G>C (p.Glu336Asp)
c.960G>C (p.Glu320Asp)
c.885G>C (p.Glu295Asp)
c.828G>C (p.Glu276Asp)
3g.30672116G=CA1354873137TGFBR2c.933G= (p.Glu311=)
n.2529G=
c.1008G= (p.Glu336=)
c.960G= (p.Glu320=)
c.885G= (p.Glu295=)
c.828G= (p.Glu276=)
3g.30672116G>TCA351808198TGFBR2c.933G>T (p.Glu311Asp)
n.2529G>T
c.1008G>T (p.Glu336Asp)
c.960G>T (p.Glu320Asp)
c.885G>T (p.Glu295Asp)
c.828G>T (p.Glu276Asp)
3g.30672119_30672138delCA541976297TGFBR2c.936_955del (p.Arg313ThrfsTer?)
n.2532_2551del
c.1011_1030del (p.Arg338ThrfsTer?)
c.963_982del (p.Arg322ThrfsTer?)
c.888_907del (p.Arg297ThrfsTer?)
c.831_850del (p.Arg278ThrfsTer?)
 dbSNP gnomAD v2 gnomAD v4
3g.30672117G>ACA020552TGFBR2c.934G>A (p.Glu312Lys)
n.2530G>A
c.1009G>A (p.Glu337Lys)
c.961G>A (p.Glu321Lys)
c.886G>A (p.Glu296Lys)
c.829G>A (p.Glu277Lys)
 ClinVar dbSNP gnomAD v4
3g.30672117G>CCA351808199TGFBR2c.934G>C (p.Glu312Gln)
n.2530G>C
c.1009G>C (p.Glu337Gln)
c.961G>C (p.Glu321Gln)
c.886G>C (p.Glu296Gln)
c.829G>C (p.Glu277Gln)
 dbSNP
3g.30672117G=CA1354873138TGFBR2c.934G= (p.Glu312=)
n.2530G=
c.1009G= (p.Glu337=)
c.961G= (p.Glu321=)
c.886G= (p.Glu296=)
c.829G= (p.Glu277=)
3g.30672117G>TCA351808200TGFBR2c.934G>T (p.Glu312Ter)
n.2530G>T
c.1009G>T (p.Glu337Ter)
c.961G>T (p.Glu321Ter)
c.886G>T (p.Glu296Ter)
c.829G>T (p.Glu277Ter)
 dbSNP
3g.30672118A>CCA351808203TGFBR2c.935A>C (p.Glu312Ala)
n.2531A>C
c.1010A>C (p.Glu337Ala)
c.962A>C (p.Glu321Ala)
c.887A>C (p.Glu296Ala)
c.830A>C (p.Glu277Ala)
3g.30672118A>GCA351808202TGFBR2c.935A>G (p.Glu312Gly)
n.2531A>G
c.1010A>G (p.Glu337Gly)
c.962A>G (p.Glu321Gly)
c.887A>G (p.Glu296Gly)
c.830A>G (p.Glu277Gly)
 dbSNP
3g.30672118A>TCA351808201TGFBR2c.935A>T (p.Glu312Val)
n.2531A>T
c.1010A>T (p.Glu337Val)
c.962A>T (p.Glu321Val)
c.887A>T (p.Glu296Val)
c.830A>T (p.Glu277Val)
 dbSNP
3g.30672119G>ACA433058911TGFBR2c.936G>A (p.Glu312=)
n.2532G>A
c.1011G>A (p.Glu337=)
c.963G>A (p.Glu321=)
c.888G>A (p.Glu296=)
c.831G>A (p.Glu277=)
 dbSNP
3g.30672119G>CCA351808204TGFBR2c.936G>C (p.Glu312Asp)
n.2532G>C
c.1011G>C (p.Glu337Asp)
c.963G>C (p.Glu321Asp)
c.888G>C (p.Glu296Asp)
c.831G>C (p.Glu277Asp)
 dbSNP
3g.30672119G>TCA351808205TGFBR2c.936G>T (p.Glu312Asp)
n.2532G>T
c.1011G>T (p.Glu337Asp)
c.963G>T (p.Glu321Asp)
c.888G>T (p.Glu296Asp)
c.831G>T (p.Glu277Asp)
 gnomAD v4
3g.30672120C>ACA433058913TGFBR2c.937C>A (p.Arg313=)
n.2533C>A
c.1012C>A (p.Arg338=)
c.964C>A (p.Arg322=)
c.889C>A (p.Arg297=)
c.832C>A (p.Arg278=)
 dbSNP
3g.30672120C=CA1354873139TGFBR2c.937C= (p.Arg313=)
n.2533C=
c.1012C= (p.Arg338=)
c.964C= (p.Arg322=)
c.889C= (p.Arg297=)
c.832C= (p.Arg278=)
3g.30672120C>GCA351808206TGFBR2c.937C>G (p.Arg313Gly)
n.2533C>G
c.1012C>G (p.Arg338Gly)
c.964C>G (p.Arg322Gly)
c.889C>G (p.Arg297Gly)
c.832C>G (p.Arg278Gly)
 ClinVar dbSNP
3g.30672120C>TCA71528357TGFBR2c.937C>T (p.Arg313Trp)
n.2533C>T
c.1012C>T (p.Arg338Trp)
c.964C>T (p.Arg322Trp)
c.889C>T (p.Arg297Trp)
c.832C>T (p.Arg278Trp)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672121G>ACA050250TGFBR2c.938G>A (p.Arg313Gln)
n.2534G>A
c.1013G>A (p.Arg338Gln)
c.965G>A (p.Arg322Gln)
c.890G>A (p.Arg297Gln)
c.833G>A (p.Arg278Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672121G>CCA351808207TGFBR2c.938G>C (p.Arg313Pro)
n.2534G>C
c.1013G>C (p.Arg338Pro)
c.965G>C (p.Arg322Pro)
c.890G>C (p.Arg297Pro)
c.833G>C (p.Arg278Pro)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672121G=CA1354873140TGFBR2c.938G= (p.Arg313=)
n.2534G=
c.1013G= (p.Arg338=)
c.965G= (p.Arg322=)
c.890G= (p.Arg297=)
c.833G= (p.Arg278=)
3g.30672121G>TCA050258TGFBR2c.938G>T (p.Arg313Leu)
n.2534G>T
c.1013G>T (p.Arg338Leu)
c.965G>T (p.Arg322Leu)
c.890G>T (p.Arg297Leu)
c.833G>T (p.Arg278Leu)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672122G>ACA433058914TGFBR2c.939G>A (p.Arg313=)
n.2535G>A
c.1014G>A (p.Arg338=)
c.966G>A (p.Arg322=)
c.891G>A (p.Arg297=)
c.834G>A (p.Arg278=)
 dbSNP
3g.30672122G>CCA433058916TGFBR2c.939G>C (p.Arg313=)
n.2535G>C
c.1014G>C (p.Arg338=)
c.966G>C (p.Arg322=)
c.891G>C (p.Arg297=)
c.834G>C (p.Arg278=)
 dbSNP
3g.30672122G=CA1354873141TGFBR2c.939G= (p.Arg313=)
n.2535G=
c.1014G= (p.Arg338=)
c.966G= (p.Arg322=)
c.891G= (p.Arg297=)
c.834G= (p.Arg278=)
3g.30672122G>TCA433058915TGFBR2c.939G>T (p.Arg313=)
n.2535G>T
c.1014G>T (p.Arg338=)
c.966G>T (p.Arg322=)
c.891G>T (p.Arg297=)
c.834G>T (p.Arg278=)
 ClinVar dbSNP
3g.30672123A>CCA351808208TGFBR2c.940A>C (p.Lys314Gln)
n.2536A>C
c.1015A>C (p.Lys339Gln)
c.967A>C (p.Lys323Gln)
c.892A>C (p.Lys298Gln)
c.835A>C (p.Lys279Gln)
3g.30672123A>GCA351808209TGFBR2c.940A>G (p.Lys314Glu)
n.2536A>G
c.1015A>G (p.Lys339Glu)
c.967A>G (p.Lys323Glu)
c.892A>G (p.Lys298Glu)
c.835A>G (p.Lys279Glu)
3g.30672123A>TCA351808210TGFBR2c.940A>T (p.Lys314Ter)
n.2536A>T
c.1015A>T (p.Lys339Ter)
c.967A>T (p.Lys323Ter)
c.892A>T (p.Lys298Ter)
c.835A>T (p.Lys279Ter)
 dbSNP
3g.30672124A>CCA351808211TGFBR2c.941A>C (p.Lys314Thr)
n.2537A>C
c.1016A>C (p.Lys339Thr)
c.968A>C (p.Lys323Thr)
c.893A>C (p.Lys298Thr)
c.836A>C (p.Lys279Thr)
3g.30672124A>GCA351808212TGFBR2c.941A>G (p.Lys314Arg)
n.2537A>G
c.1016A>G (p.Lys339Arg)
c.968A>G (p.Lys323Arg)
c.893A>G (p.Lys298Arg)
c.836A>G (p.Lys279Arg)
 dbSNP
3g.30672124A>TCA351808213TGFBR2c.941A>T (p.Lys314Met)
n.2537A>T
c.1016A>T (p.Lys339Met)
c.968A>T (p.Lys323Met)
c.893A>T (p.Lys298Met)
c.836A>T (p.Lys279Met)
 dbSNP
3g.30672125G>ACA433058918TGFBR2c.942G>A (p.Lys314=)
n.2538G>A
c.1017G>A (p.Lys339=)
c.969G>A (p.Lys323=)
c.894G>A (p.Lys298=)
c.837G>A (p.Lys279=)
 dbSNP gnomAD v4
3g.30672125G>CCA351808215TGFBR2c.942G>C (p.Lys314Asn)
n.2538G>C
c.1017G>C (p.Lys339Asn)
c.969G>C (p.Lys323Asn)
c.894G>C (p.Lys298Asn)
c.837G>C (p.Lys279Asn)
 dbSNP
3g.30672125G>TCA351808214TGFBR2c.942G>T (p.Lys314Asn)
n.2538G>T
c.1017G>T (p.Lys339Asn)
c.969G>T (p.Lys323Asn)
c.894G>T (p.Lys298Asn)
c.837G>T (p.Lys279Asn)
3g.30672126A>CCA351808216TGFBR2c.943A>C (p.Thr315Pro)
n.2539A>C
c.1018A>C (p.Thr340Pro)
c.970A>C (p.Thr324Pro)
c.895A>C (p.Thr299Pro)
c.838A>C (p.Thr280Pro)
 dbSNP
3g.30672126A>GCA351808217TGFBR2c.943A>G (p.Thr315Ala)
n.2539A>G
c.1018A>G (p.Thr340Ala)
c.970A>G (p.Thr324Ala)
c.895A>G (p.Thr299Ala)
c.838A>G (p.Thr280Ala)
 dbSNP
3g.30672126A>TCA351808218TGFBR2c.943A>T (p.Thr315Ser)
n.2539A>T
c.1018A>T (p.Thr340Ser)
c.970A>T (p.Thr324Ser)
c.895A>T (p.Thr299Ser)
c.838A>T (p.Thr280Ser)
 dbSNP
3g.30672127C>ACA351808219TGFBR2c.944C>A (p.Thr315Lys)
n.2540C>A
c.1019C>A (p.Thr340Lys)
c.971C>A (p.Thr324Lys)
c.896C>A (p.Thr299Lys)
c.839C>A (p.Thr280Lys)
 dbSNP
3g.30672127C=CA1354873142TGFBR2c.944C= (p.Thr315=)
n.2540C=
c.1019C= (p.Thr340=)
c.971C= (p.Thr324=)
c.896C= (p.Thr299=)
c.839C= (p.Thr280=)
3g.30672127C>GCA351808220TGFBR2c.944C>G (p.Thr315Arg)
n.2540C>G
c.1019C>G (p.Thr340Arg)
c.971C>G (p.Thr324Arg)
c.896C>G (p.Thr299Arg)
c.839C>G (p.Thr280Arg)
 dbSNP
3g.30672127C>TCA020555TGFBR2c.944C>T (p.Thr315Met)
n.2540C>T
c.1019C>T (p.Thr340Met)
c.971C>T (p.Thr324Met)
c.896C>T (p.Thr299Met)
c.839C>T (p.Thr280Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672128G>ACA71528404TGFBR2c.945G>A (p.Thr315=)
n.2541G>A
c.1020G>A (p.Thr340=)
c.972G>A (p.Thr324=)
c.897G>A (p.Thr299=)
c.840G>A (p.Thr280=)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672128G>CCA433058919TGFBR2c.945G>C (p.Thr315=)
n.2541G>C
c.1020G>C (p.Thr340=)
c.972G>C (p.Thr324=)
c.897G>C (p.Thr299=)
c.840G>C (p.Thr280=)
 dbSNP gnomAD v4
3g.30672128G=CA1354873143TGFBR2c.945G= (p.Thr315=)
n.2541G=
c.1020G= (p.Thr340=)
c.972G= (p.Thr324=)
c.897G= (p.Thr299=)
c.840G= (p.Thr280=)
3g.30672128G>TCA433058920TGFBR2c.945G>T (p.Thr315=)
n.2541G>T
c.1020G>T (p.Thr340=)
c.972G>T (p.Thr324=)
c.897G>T (p.Thr299=)
c.840G>T (p.Thr280=)
 dbSNP gnomAD v2 gnomAD v4
3g.30672129G>ACA351808221TGFBR2c.946G>A (p.Glu316Lys)
n.2542G>A
c.1021G>A (p.Glu341Lys)
c.973G>A (p.Glu325Lys)
c.898G>A (p.Glu300Lys)
c.841G>A (p.Glu281Lys)
 dbSNP
3g.30672129G>CCA351808222TGFBR2c.946G>C (p.Glu316Gln)
n.2542G>C
c.1021G>C (p.Glu341Gln)
c.973G>C (p.Glu325Gln)
c.898G>C (p.Glu300Gln)
c.841G>C (p.Glu281Gln)
 dbSNP
3g.30672129G>TCA351808223TGFBR2c.946G>T (p.Glu316Ter)
n.2542G>T
c.1021G>T (p.Glu341Ter)
c.973G>T (p.Glu325Ter)
c.898G>T (p.Glu300Ter)
c.841G>T (p.Glu281Ter)
 dbSNP
3g.30672130A=CA2580587341TGFBR2c.947A= (p.Glu316=)
n.2543A=
c.1022A= (p.Glu341=)
c.974A= (p.Glu325=)
c.899A= (p.Glu300=)
c.842A= (p.Glu281=)
3g.30672130A>CCA351808224TGFBR2c.947A>C (p.Glu316Ala)
n.2543A>C
c.1022A>C (p.Glu341Ala)
c.974A>C (p.Glu325Ala)
c.899A>C (p.Glu300Ala)
c.842A>C (p.Glu281Ala)
3g.30672130A>GCA351808225TGFBR2c.947A>G (p.Glu316Gly)
n.2543A>G
c.1022A>G (p.Glu341Gly)
c.974A>G (p.Glu325Gly)
c.899A>G (p.Glu300Gly)
c.842A>G (p.Glu281Gly)
 dbSNP gnomAD v4
3g.30672130A>TCA71528409TGFBR2c.947A>T (p.Glu316Val)
n.2543A>T
c.1022A>T (p.Glu341Val)
c.974A>T (p.Glu325Val)
c.899A>T (p.Glu300Val)
c.842A>T (p.Glu281Val)
 dbSNP
3g.30672131G>ACA433058922TGFBR2c.948G>A (p.Glu316=)
n.2544G>A
c.1023G>A (p.Glu341=)
c.975G>A (p.Glu325=)
c.900G>A (p.Glu300=)
c.843G>A (p.Glu281=)
 ClinVar dbSNP gnomAD v4
3g.30672131G>CCA351808226TGFBR2c.948G>C (p.Glu316Asp)
n.2544G>C
c.1023G>C (p.Glu341Asp)
c.975G>C (p.Glu325Asp)
c.900G>C (p.Glu300Asp)
c.843G>C (p.Glu281Asp)
 dbSNP
3g.30672131G=CA1354873144TGFBR2c.948G= (p.Glu316=)
n.2544G=
c.1023G= (p.Glu341=)
c.975G= (p.Glu325=)
c.900G= (p.Glu300=)
c.843G= (p.Glu281=)
3g.30672131G>TCA351808227TGFBR2c.948G>T (p.Glu316Asp)
n.2544G>T
c.1023G>T (p.Glu341Asp)
c.975G>T (p.Glu325Asp)
c.900G>T (p.Glu300Asp)
c.843G>T (p.Glu281Asp)
 dbSNP
3g.30672132T>ACA351808229TGFBR2c.949T>A (p.Leu317Met)
n.2545T>A
c.1024T>A (p.Leu342Met)
c.976T>A (p.Leu326Met)
c.901T>A (p.Leu301Met)
c.844T>A (p.Leu282Met)
 dbSNP
3g.30672132T>CCA433058947TGFBR2c.949T>C (p.Leu317=)
n.2545T>C
c.1024T>C (p.Leu342=)
c.976T>C (p.Leu326=)
c.901T>C (p.Leu301=)
c.844T>C (p.Leu282=)
 ClinVar dbSNP COSMIC COSMIC
3g.30672132T>GCA351808228TGFBR2c.949T>G (p.Leu317Val)
n.2545T>G
c.1024T>G (p.Leu342Val)
c.976T>G (p.Leu326Val)
c.901T>G (p.Leu301Val)
c.844T>G (p.Leu282Val)
 dbSNP
3g.30672132T=CA1354873145TGFBR2c.949T= (p.Leu317=)
n.2545T=
c.1024T= (p.Leu342=)
c.976T= (p.Leu326=)
c.901T= (p.Leu301=)
c.844T= (p.Leu282=)
3g.30672133T>ACA351808230TGFBR2c.950T>A (p.Leu317Ter)
n.2546T>A
c.1025T>A (p.Leu342Ter)
c.977T>A (p.Leu326Ter)
c.902T>A (p.Leu301Ter)
c.845T>A (p.Leu282Ter)
3g.30672133T>CCA351808231TGFBR2c.950T>C (p.Leu317Ser)
n.2546T>C
c.1025T>C (p.Leu342Ser)
c.977T>C (p.Leu326Ser)
c.902T>C (p.Leu301Ser)
c.845T>C (p.Leu282Ser)
3g.30672133T>GCA351808232TGFBR2c.950T>G (p.Leu317Trp)
n.2546T>G
c.1025T>G (p.Leu342Trp)
c.977T>G (p.Leu326Trp)
c.902T>G (p.Leu301Trp)
c.845T>G (p.Leu282Trp)
3g.30672134G>ACA433058948TGFBR2c.951G>A (p.Leu317=)
n.2547G>A
c.1026G>A (p.Leu342=)
c.978G>A (p.Leu326=)
c.903G>A (p.Leu301=)
c.846G>A (p.Leu282=)
 ClinVar dbSNP
3g.30672134G>CCA351808233TGFBR2c.951G>C (p.Leu317Phe)
n.2547G>C
c.1026G>C (p.Leu342Phe)
c.978G>C (p.Leu326Phe)
c.903G>C (p.Leu301Phe)
c.846G>C (p.Leu282Phe)
 dbSNP
3g.30672134G>TCA351808234TGFBR2c.951G>T (p.Leu317Phe)
n.2547G>T
c.1026G>T (p.Leu342Phe)
c.978G>T (p.Leu326Phe)
c.903G>T (p.Leu301Phe)
c.846G>T (p.Leu282Phe)
 dbSNP gnomAD v4
3g.30672137delCA645535106TGFBR2c.954del (p.Lys319AsnfsTer5)
n.2550del
c.1029del (p.Lys344AsnfsTer5)
c.981del (p.Lys328AsnfsTer5)
c.906del (p.Lys303AsnfsTer5)
c.849del (p.Lys284AsnfsTer5)
 COSMIC COSMIC
3g.30672135G>ACA351808237TGFBR2c.952G>A (p.Gly318Arg)
n.2548G>A
c.1027G>A (p.Gly343Arg)
c.979G>A (p.Gly327Arg)
c.904G>A (p.Gly302Arg)
c.847G>A (p.Gly283Arg)
 dbSNP
3g.30672135G>CCA351808236TGFBR2c.952G>C (p.Gly318Arg)
n.2548G>C
c.1027G>C (p.Gly343Arg)
c.979G>C (p.Gly327Arg)
c.904G>C (p.Gly302Arg)
c.847G>C (p.Gly283Arg)
 dbSNP
3g.30672135G>TCA351808235TGFBR2c.952G>T (p.Gly318Trp)
n.2548G>T
c.1027G>T (p.Gly343Trp)
c.979G>T (p.Gly327Trp)
c.904G>T (p.Gly302Trp)
c.847G>T (p.Gly283Trp)
 dbSNP
3g.30672136G>ACA351808238TGFBR2c.953G>A (p.Gly318Glu)
n.2549G>A
c.1028G>A (p.Gly343Glu)
c.980G>A (p.Gly327Glu)
c.905G>A (p.Gly302Glu)
c.848G>A (p.Gly283Glu)
 dbSNP
3g.30672136G>CCA050632TGFBR2c.953G>C (p.Gly318Ala)
n.2549G>C
c.1028G>C (p.Gly343Ala)
c.980G>C (p.Gly327Ala)
c.905G>C (p.Gly302Ala)
c.848G>C (p.Gly283Ala)
 ClinVar dbSNP ExAC gnomAD v3 gnomAD v4
3g.30672136G=CA1354873146TGFBR2c.953G= (p.Gly318=)
n.2549G=
c.1028G= (p.Gly343=)
c.980G= (p.Gly327=)
c.905G= (p.Gly302=)
c.848G= (p.Gly283=)
3g.30672136G>TCA351808239TGFBR2c.953G>T (p.Gly318Val)
n.2549G>T
c.1028G>T (p.Gly343Val)
c.980G>T (p.Gly327Val)
c.905G>T (p.Gly302Val)
c.848G>T (p.Gly283Val)
 dbSNP
3g.30672137G>ACA433058949TGFBR2c.954G>A (p.Gly318=)
n.2550G>A
c.1029G>A (p.Gly343=)
c.981G>A (p.Gly327=)
c.906G>A (p.Gly302=)
c.849G>A (p.Gly283=)
 ClinVar dbSNP gnomAD v4 COSMIC COSMIC
3g.30672137G>CCA433058950TGFBR2c.954G>C (p.Gly318=)
n.2550G>C
c.1029G>C (p.Gly343=)
c.981G>C (p.Gly327=)
c.906G>C (p.Gly302=)
c.849G>C (p.Gly283=)
 dbSNP
3g.30672137G>TCA433058951TGFBR2c.954G>T (p.Gly318=)
n.2550G>T
c.1029G>T (p.Gly343=)
c.981G>T (p.Gly327=)
c.906G>T (p.Gly302=)
c.849G>T (p.Gly283=)
3g.30672138A>CCA351808240TGFBR2c.955A>C (p.Lys319Gln)
n.2551A>C
c.1030A>C (p.Lys344Gln)
c.982A>C (p.Lys328Gln)
c.907A>C (p.Lys303Gln)
c.850A>C (p.Lys284Gln)
3g.30672138A>GCA351808241TGFBR2c.955A>G (p.Lys319Glu)
n.2551A>G
c.1030A>G (p.Lys344Glu)
c.982A>G (p.Lys328Glu)
c.907A>G (p.Lys303Glu)
c.850A>G (p.Lys284Glu)
 dbSNP
3g.30672138A>TCA351808242TGFBR2c.955A>T (p.Lys319Ter)
n.2551A>T
c.1030A>T (p.Lys344Ter)
c.982A>T (p.Lys328Ter)
c.907A>T (p.Lys303Ter)
c.850A>T (p.Lys284Ter)
3g.30672139A=CA1354873147TGFBR2c.956A= (p.Lys319=)
n.2552A=
c.1031A= (p.Lys344=)
c.983A= (p.Lys328=)
c.908A= (p.Lys303=)
c.851A= (p.Lys284=)
3g.30672139A>CCA351808245TGFBR2c.956A>C (p.Lys319Thr)
n.2552A>C
c.1031A>C (p.Lys344Thr)
c.983A>C (p.Lys328Thr)
c.908A>C (p.Lys303Thr)
c.851A>C (p.Lys284Thr)
 gnomAD v4
3g.30672139A>GCA351808243TGFBR2c.956A>G (p.Lys319Arg)
n.2552A>G
c.1031A>G (p.Lys344Arg)
c.983A>G (p.Lys328Arg)
c.908A>G (p.Lys303Arg)
c.851A>G (p.Lys284Arg)
 ClinVar dbSNP
3g.30672139A>TCA351808244TGFBR2c.956A>T (p.Lys319Ile)
n.2552A>T
c.1031A>T (p.Lys344Ile)
c.983A>T (p.Lys328Ile)
c.908A>T (p.Lys303Ile)
c.851A>T (p.Lys284Ile)
3g.30672140A=CA1354873148TGFBR2c.957A= (p.Lys319=)
n.2553A=
c.1032A= (p.Lys344=)
c.984A= (p.Lys328=)
c.909A= (p.Lys303=)
c.852A= (p.Lys284=)
3g.30672140A>CCA16621992TGFBR2c.957A>C (p.Lys319Asn)
n.2553A>C
c.1032A>C (p.Lys344Asn)
c.984A>C (p.Lys328Asn)
c.909A>C (p.Lys303Asn)
c.852A>C (p.Lys284Asn)
 dbSNP gnomAD v3 gnomAD v4
3g.30672140A>GCA433058952TGFBR2c.957A>G (p.Lys319=)
n.2553A>G
c.1032A>G (p.Lys344=)
c.984A>G (p.Lys328=)
c.909A>G (p.Lys303=)
c.852A>G (p.Lys284=)
 dbSNP gnomAD v4
3g.30672140A>TCA351808246TGFBR2c.957A>T (p.Lys319Asn)
n.2553A>T
c.1032A>T (p.Lys344Asn)
c.984A>T (p.Lys328Asn)
c.909A>T (p.Lys303Asn)
c.852A>T (p.Lys284Asn)
 dbSNP
3g.30672141C>ACA351808247TGFBR2c.958C>A (p.Gln320Lys)
n.2554C>A
c.1033C>A (p.Gln345Lys)
c.985C>A (p.Gln329Lys)
c.910C>A (p.Gln304Lys)
c.853C>A (p.Gln285Lys)
 dbSNP
3g.30672141C>GCA351808248TGFBR2c.958C>G (p.Gln320Glu)
n.2554C>G
c.1033C>G (p.Gln345Glu)
c.985C>G (p.Gln329Glu)
c.910C>G (p.Gln304Glu)
c.853C>G (p.Gln285Glu)
 dbSNP
3g.30672141C>TCA351808249TGFBR2c.958C>T (p.Gln320Ter)
n.2554C>T
c.1033C>T (p.Gln345Ter)
c.985C>T (p.Gln329Ter)
c.910C>T (p.Gln304Ter)
c.853C>T (p.Gln285Ter)
 dbSNP
3g.30672142A>CCA351808250TGFBR2c.959A>C (p.Gln320Pro)
n.2555A>C
c.1034A>C (p.Gln345Pro)
c.986A>C (p.Gln329Pro)
c.911A>C (p.Gln304Pro)
c.854A>C (p.Gln285Pro)
3g.30672142A>GCA351808251TGFBR2c.959A>G (p.Gln320Arg)
n.2555A>G
c.1034A>G (p.Gln345Arg)
c.986A>G (p.Gln329Arg)
c.911A>G (p.Gln304Arg)
c.854A>G (p.Gln285Arg)
3g.30672142A>TCA351808252TGFBR2c.959A>T (p.Gln320Leu)
n.2555A>T
c.1034A>T (p.Gln345Leu)
c.986A>T (p.Gln329Leu)
c.911A>T (p.Gln304Leu)
c.854A>T (p.Gln285Leu)
3g.30672143A=CA1354873149TGFBR2c.960A= (p.Gln320=)
n.2556A=
c.1035A= (p.Gln345=)
c.987A= (p.Gln329=)
c.912A= (p.Gln304=)
c.855A= (p.Gln285=)
3g.30672143A>CCA351808253TGFBR2c.960A>C (p.Gln320His)
n.2556A>C
c.1035A>C (p.Gln345His)
c.987A>C (p.Gln329His)
c.912A>C (p.Gln304His)
c.855A>C (p.Gln285His)
 ClinVar gnomAD v4
3g.30672143A>GCA433058953TGFBR2c.960A>G (p.Gln320=)
n.2556A>G
c.1035A>G (p.Gln345=)
c.987A>G (p.Gln329=)
c.912A>G (p.Gln304=)
c.855A>G (p.Gln285=)
 ClinVar dbSNP
3g.30672143A>TCA351808254TGFBR2c.960A>T (p.Gln320His)
n.2556A>T
c.1035A>T (p.Gln345His)
c.987A>T (p.Gln329His)
c.912A>T (p.Gln304His)
c.855A>T (p.Gln285His)
3g.30672144T>ACA351808255TGFBR2c.961T>A (p.Tyr321Asn)
n.2557T>A
c.1036T>A (p.Tyr346Asn)
c.988T>A (p.Tyr330Asn)
c.913T>A (p.Tyr305Asn)
c.856T>A (p.Tyr286Asn)
 dbSNP
3g.30672144T>CCA351808256TGFBR2c.961T>C (p.Tyr321His)
n.2557T>C
c.1036T>C (p.Tyr346His)
c.988T>C (p.Tyr330His)
c.913T>C (p.Tyr305His)
c.856T>C (p.Tyr286His)
 dbSNP
3g.30672144T>GCA351808257TGFBR2c.961T>G (p.Tyr321Asp)
n.2557T>G
c.1036T>G (p.Tyr346Asp)
c.988T>G (p.Tyr330Asp)
c.913T>G (p.Tyr305Asp)
c.856T>G (p.Tyr286Asp)
 ClinVar dbSNP
3g.30672144T=CA1354873150TGFBR2c.961T= (p.Tyr321=)
n.2557T=
c.1036T= (p.Tyr346=)
c.988T= (p.Tyr330=)
c.913T= (p.Tyr305=)
c.856T= (p.Tyr286=)
3g.30672145A=CA1354873151TGFBR2c.962A= (p.Tyr321=)
n.2558A=
c.1037A= (p.Tyr346=)
c.989A= (p.Tyr330=)
c.914A= (p.Tyr305=)
c.857A= (p.Tyr286=)
3g.30672145A>CCA351808260TGFBR2c.962A>C (p.Tyr321Ser)
n.2558A>C
c.1037A>C (p.Tyr346Ser)
c.989A>C (p.Tyr330Ser)
c.914A>C (p.Tyr305Ser)
c.857A>C (p.Tyr286Ser)
3g.30672145A>GCA351808259TGFBR2c.962A>G (p.Tyr321Cys)
n.2558A>G
c.1037A>G (p.Tyr346Cys)
c.989A>G (p.Tyr330Cys)
c.914A>G (p.Tyr305Cys)
c.857A>G (p.Tyr286Cys)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.30672145A>TCA351808258TGFBR2c.962A>T (p.Tyr321Phe)
n.2558A>T
c.1037A>T (p.Tyr346Phe)
c.989A>T (p.Tyr330Phe)
c.914A>T (p.Tyr305Phe)
c.857A>T (p.Tyr286Phe)
 dbSNP
3g.30672146C>ACA351808261TGFBR2c.963C>A (p.Tyr321Ter)
n.2559C>A
c.1038C>A (p.Tyr346Ter)
c.990C>A (p.Tyr330Ter)
c.915C>A (p.Tyr305Ter)
c.858C>A (p.Tyr286Ter)
 dbSNP
3g.30672146C>GCA351808262TGFBR2c.963C>G (p.Tyr321Ter)
n.2559C>G
c.1038C>G (p.Tyr346Ter)
c.990C>G (p.Tyr330Ter)
c.915C>G (p.Tyr305Ter)
c.858C>G (p.Tyr286Ter)
 dbSNP
3g.30672146C>TCA433058954TGFBR2c.963C>T (p.Tyr321=)
n.2559C>T
c.1038C>T (p.Tyr346=)
c.990C>T (p.Tyr330=)
c.915C>T (p.Tyr305=)
c.858C>T (p.Tyr286=)
 dbSNP
3g.30672147T>ACA351808263TGFBR2c.964T>A (p.Trp322Arg)
n.2560T>A
c.1039T>A (p.Trp347Arg)
c.991T>A (p.Trp331Arg)
c.916T>A (p.Trp306Arg)
c.859T>A (p.Trp287Arg)
3g.30672147T>CCA351808264TGFBR2c.964T>C (p.Trp322Arg)
n.2560T>C
c.1039T>C (p.Trp347Arg)
c.991T>C (p.Trp331Arg)
c.916T>C (p.Trp306Arg)
c.859T>C (p.Trp287Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.30672147T>GCA321434TGFBR2c.964T>G (p.Trp322Gly)
n.2560T>G
c.1039T>G (p.Trp347Gly)
c.991T>G (p.Trp331Gly)
c.916T>G (p.Trp306Gly)
c.859T>G (p.Trp287Gly)
 ClinVar dbSNP
3g.30672147T=CA1354873152TGFBR2c.964T= (p.Trp322=)
n.2560T=
c.1039T= (p.Trp347=)
c.991T= (p.Trp331=)
c.916T= (p.Trp306=)
c.859T= (p.Trp287=)
3g.30672148G>ACA351808265TGFBR2c.965G>A (p.Trp322Ter)
n.2561G>A
c.1040G>A (p.Trp347Ter)
c.992G>A (p.Trp331Ter)
c.917G>A (p.Trp306Ter)
c.860G>A (p.Trp287Ter)
 gnomAD v4
3g.30672148G>CCA351808266TGFBR2c.965G>C (p.Trp322Ser)
n.2561G>C
c.1040G>C (p.Trp347Ser)
c.992G>C (p.Trp331Ser)
c.917G>C (p.Trp306Ser)
c.860G>C (p.Trp287Ser)
3g.30672148G>TCA351808267TGFBR2c.965G>T (p.Trp322Leu)
n.2561G>T
c.1040G>T (p.Trp347Leu)
c.992G>T (p.Trp331Leu)
c.917G>T (p.Trp306Leu)
c.860G>T (p.Trp287Leu)
3g.30672149delCA2702371006TGFBR2c.966del (p.Trp322CysfsTer2)
n.2562del
c.1041del (p.Trp347CysfsTer2)
c.993del (p.Trp331CysfsTer2)
c.918del (p.Trp306CysfsTer2)
c.861del (p.Trp287CysfsTer2)
 dbSNP
3g.30672149G>ACA351808268TGFBR2c.966G>A (p.Trp322Ter)
n.2562G>A
c.1041G>A (p.Trp347Ter)
c.993G>A (p.Trp331Ter)
c.918G>A (p.Trp306Ter)
c.861G>A (p.Trp287Ter)
 dbSNP gnomAD v4
3g.30672149G>CCA351808269TGFBR2c.966G>C (p.Trp322Cys)
n.2562G>C
c.1041G>C (p.Trp347Cys)
c.993G>C (p.Trp331Cys)
c.918G>C (p.Trp306Cys)
c.861G>C (p.Trp287Cys)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672149G=CA1354873153TGFBR2c.966G= (p.Trp322=)
n.2562G=
c.1041G= (p.Trp347=)
c.993G= (p.Trp331=)
c.918G= (p.Trp306=)
c.861G= (p.Trp287=)
3g.30672149G>TCA351808270TGFBR2c.966G>T (p.Trp322Cys)
n.2562G>T
c.1041G>T (p.Trp347Cys)
c.993G>T (p.Trp331Cys)
c.918G>T (p.Trp306Cys)
c.861G>T (p.Trp287Cys)
 dbSNP gnomAD v4
3g.30672150C>ACA351808271TGFBR2c.967C>A (p.Leu323Met)
n.2563C>A
c.1042C>A (p.Leu348Met)
c.994C>A (p.Leu332Met)
c.919C>A (p.Leu307Met)
c.862C>A (p.Leu288Met)
 dbSNP
3g.30672150C=CA1354873154TGFBR2c.967C= (p.Leu323=)
n.2563C=
c.1042C= (p.Leu348=)
c.994C= (p.Leu332=)
c.919C= (p.Leu307=)
c.862C= (p.Leu288=)
3g.30672150C>GCA050696TGFBR2c.967C>G (p.Leu323Val)
n.2563C>G
c.1042C>G (p.Leu348Val)
c.994C>G (p.Leu332Val)
c.919C>G (p.Leu307Val)
c.862C>G (p.Leu288Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672150C>TCA433058956TGFBR2c.967C>T (p.Leu323=)
n.2563C>T
c.1042C>T (p.Leu348=)
c.994C>T (p.Leu332=)
c.919C>T (p.Leu307=)
c.862C>T (p.Leu288=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672151T>ACA351808274TGFBR2c.968T>A (p.Leu323Gln)
n.2564T>A
c.1043T>A (p.Leu348Gln)
c.995T>A (p.Leu332Gln)
c.920T>A (p.Leu307Gln)
c.863T>A (p.Leu288Gln)
 dbSNP
3g.30672151T>CCA351808273TGFBR2c.968T>C (p.Leu323Pro)
n.2564T>C
c.1043T>C (p.Leu348Pro)
c.995T>C (p.Leu332Pro)
c.920T>C (p.Leu307Pro)
c.863T>C (p.Leu288Pro)
 COSMIC COSMIC
3g.30672151T>GCA351808272TGFBR2c.968T>G (p.Leu323Arg)
n.2564T>G
c.1043T>G (p.Leu348Arg)
c.995T>G (p.Leu332Arg)
c.920T>G (p.Leu307Arg)
c.863T>G (p.Leu288Arg)
 ClinVar dbSNP
3g.30672151T=CA1354873155TGFBR2c.968T= (p.Leu323=)
n.2564T=
c.1043T= (p.Leu348=)
c.995T= (p.Leu332=)
c.920T= (p.Leu307=)
c.863T= (p.Leu288=)
3g.30672152G>ACA433058957TGFBR2c.969G>A (p.Leu323=)
n.2565G>A
c.1044G>A (p.Leu348=)
c.996G>A (p.Leu332=)
c.921G>A (p.Leu307=)
c.864G>A (p.Leu288=)
 dbSNP
3g.30672152G>CCA433058958TGFBR2c.969G>C (p.Leu323=)
n.2565G>C
c.1044G>C (p.Leu348=)
c.996G>C (p.Leu332=)
c.921G>C (p.Leu307=)
c.864G>C (p.Leu288=)
 dbSNP
3g.30672152G>TCA433058959TGFBR2c.969G>T (p.Leu323=)
n.2565G>T
c.1044G>T (p.Leu348=)
c.996G>T (p.Leu332=)
c.921G>T (p.Leu307=)
c.864G>T (p.Leu288=)
3g.30672153A>CCA351808275TGFBR2c.970A>C (p.Ile324Leu)
n.2566A>C
c.1045A>C (p.Ile349Leu)
c.997A>C (p.Ile333Leu)
c.922A>C (p.Ile308Leu)
c.865A>C (p.Ile289Leu)
 dbSNP
3g.30672153A>GCA351808276TGFBR2c.970A>G (p.Ile324Val)
n.2566A>G
c.1045A>G (p.Ile349Val)
c.997A>G (p.Ile333Val)
c.922A>G (p.Ile308Val)
c.865A>G (p.Ile289Val)
 dbSNP gnomAD v4
3g.30672153A>TCA351808277TGFBR2c.970A>T (p.Ile324Phe)
n.2566A>T
c.1045A>T (p.Ile349Phe)
c.997A>T (p.Ile333Phe)
c.922A>T (p.Ile308Phe)
c.865A>T (p.Ile289Phe)
 dbSNP
3g.30672154T>ACA351808278TGFBR2c.971T>A (p.Ile324Asn)
n.2567T>A
c.1046T>A (p.Ile349Asn)
c.998T>A (p.Ile333Asn)
c.923T>A (p.Ile308Asn)
c.866T>A (p.Ile289Asn)
 dbSNP
3g.30672154T>CCA351808279TGFBR2c.971T>C (p.Ile324Thr)
n.2567T>C
c.1046T>C (p.Ile349Thr)
c.998T>C (p.Ile333Thr)
c.923T>C (p.Ile308Thr)
c.866T>C (p.Ile289Thr)
 dbSNP
3g.30672154T>GCA351808280TGFBR2c.971T>G (p.Ile324Ser)
n.2567T>G
c.1046T>G (p.Ile349Ser)
c.998T>G (p.Ile333Ser)
c.923T>G (p.Ile308Ser)
c.866T>G (p.Ile289Ser)
 dbSNP
3g.30672155C>ACA433058960TGFBR2c.972C>A (p.Ile324=)
n.2568C>A
c.1047C>A (p.Ile349=)
c.999C>A (p.Ile333=)
c.924C>A (p.Ile308=)
c.867C>A (p.Ile289=)
 dbSNP
3g.30672155C>GCA351808281TGFBR2c.972C>G (p.Ile324Met)
n.2568C>G
c.1047C>G (p.Ile349Met)
c.999C>G (p.Ile333Met)
c.924C>G (p.Ile308Met)
c.867C>G (p.Ile289Met)
 ClinVar dbSNP gnomAD v4
3g.30672155C>TCA433058961TGFBR2c.972C>T (p.Ile324=)
n.2568C>T
c.1047C>T (p.Ile349=)
c.999C>T (p.Ile333=)
c.924C>T (p.Ile308=)
c.867C>T (p.Ile289=)
 dbSNP
3g.30672156_30672158delCA923726382TGFBR2c.973_975del (p.Thr325del)
n.2569_2571del
c.1048_1050del (p.Thr350del)
c.1000_1002del (p.Thr334del)
c.925_927del (p.Thr309del)
c.868_870del (p.Thr290del)
3g.30672156A>CCA351808282TGFBR2c.973A>C (p.Thr325Pro)
n.2569A>C
c.1048A>C (p.Thr350Pro)
c.1000A>C (p.Thr334Pro)
c.925A>C (p.Thr309Pro)
c.868A>C (p.Thr290Pro)
 dbSNP
3g.30672156A>GCA351808283TGFBR2c.973A>G (p.Thr325Ala)
n.2569A>G
c.1048A>G (p.Thr350Ala)
c.1000A>G (p.Thr334Ala)
c.925A>G (p.Thr309Ala)
c.868A>G (p.Thr290Ala)
3g.30672156A>TCA351808284TGFBR2c.973A>T (p.Thr325Ser)
n.2569A>T
c.1048A>T (p.Thr350Ser)
c.1000A>T (p.Thr334Ser)
c.925A>T (p.Thr309Ser)
c.868A>T (p.Thr290Ser)
 dbSNP
3g.30672157C>ACA351808285TGFBR2c.974C>A (p.Thr325Asn)
n.2570C>A
c.1049C>A (p.Thr350Asn)
c.1001C>A (p.Thr334Asn)
c.926C>A (p.Thr309Asn)
c.869C>A (p.Thr290Asn)
 dbSNP
3g.30672157C>GCA351808286TGFBR2c.974C>G (p.Thr325Ser)
n.2570C>G
c.1049C>G (p.Thr350Ser)
c.1001C>G (p.Thr334Ser)
c.926C>G (p.Thr309Ser)
c.869C>G (p.Thr290Ser)
 dbSNP
3g.30672157C>TCA351808287TGFBR2c.974C>T (p.Thr325Ile)
n.2570C>T
c.1049C>T (p.Thr350Ile)
c.1001C>T (p.Thr334Ile)
c.926C>T (p.Thr309Ile)
c.869C>T (p.Thr290Ile)
 dbSNP COSMIC COSMIC
3g.30672158C>ACA433058962TGFBR2c.975C>A (p.Thr325=)
n.2571C>A
c.1050C>A (p.Thr350=)
c.1002C>A (p.Thr334=)
c.927C>A (p.Thr309=)
c.870C>A (p.Thr290=)
 dbSNP gnomAD v4
3g.30672158C=CA1354873156TGFBR2c.975C= (p.Thr325=)
n.2571C=
c.1050C= (p.Thr350=)
c.1002C= (p.Thr334=)
c.927C= (p.Thr309=)
c.870C= (p.Thr290=)
3g.30672158C>GCA433058963TGFBR2c.975C>G (p.Thr325=)
n.2571C>G
c.1050C>G (p.Thr350=)
c.1002C>G (p.Thr334=)
c.927C>G (p.Thr309=)
c.870C>G (p.Thr290=)
 dbSNP
3g.30672158C>TCA050706TGFBR2c.975C>T (p.Thr325=)
n.2571C>T
c.1050C>T (p.Thr350=)
c.1002C>T (p.Thr334=)
c.927C>T (p.Thr309=)
c.870C>T (p.Thr290=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672159G>ACA050718TGFBR2c.976G>A (p.Ala326Thr)
n.2572G>A
c.1051G>A (p.Ala351Thr)
c.1003G>A (p.Ala335Thr)
c.928G>A (p.Ala310Thr)
c.871G>A (p.Ala291Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672159G>CCA351808289TGFBR2c.976G>C (p.Ala326Pro)
n.2572G>C
c.1051G>C (p.Ala351Pro)
c.1003G>C (p.Ala335Pro)
c.928G>C (p.Ala310Pro)
c.871G>C (p.Ala291Pro)
 dbSNP
3g.30672159G=CA1354873157TGFBR2c.976G= (p.Ala326=)
n.2572G=
c.1051G= (p.Ala351=)
c.1003G= (p.Ala335=)
c.928G= (p.Ala310=)
c.871G= (p.Ala291=)
3g.30672159G>TCA351808288TGFBR2c.976G>T (p.Ala326Ser)
n.2572G>T
c.1051G>T (p.Ala351Ser)
c.1003G>T (p.Ala335Ser)
c.928G>T (p.Ala310Ser)
c.871G>T (p.Ala291Ser)
 dbSNP
3g.30672160C>ACA351808290TGFBR2c.977C>A (p.Ala326Asp)
n.2573C>A
c.1052C>A (p.Ala351Asp)
c.1004C>A (p.Ala335Asp)
c.929C>A (p.Ala310Asp)
c.872C>A (p.Ala291Asp)
 dbSNP
3g.30672160C>GCA351808291TGFBR2c.977C>G (p.Ala326Gly)
n.2573C>G
c.1052C>G (p.Ala351Gly)
c.1004C>G (p.Ala335Gly)
c.929C>G (p.Ala310Gly)
c.872C>G (p.Ala291Gly)
 dbSNP
3g.30672160C>TCA351808292TGFBR2c.977C>T (p.Ala326Val)
n.2573C>T
c.1052C>T (p.Ala351Val)
c.1004C>T (p.Ala335Val)
c.929C>T (p.Ala310Val)
c.872C>T (p.Ala291Val)
 dbSNP gnomAD v4
3g.30672161C>ACA433058964TGFBR2c.978C>A (p.Ala326=)
n.2574C>A
c.1053C>A (p.Ala351=)
c.1005C>A (p.Ala335=)
c.930C>A (p.Ala310=)
c.873C>A (p.Ala291=)
3g.30672161C=CA1354873158TGFBR2c.978C= (p.Ala326=)
n.2574C=
c.1053C= (p.Ala351=)
c.1005C= (p.Ala335=)
c.930C= (p.Ala310=)
c.873C= (p.Ala291=)
3g.30672161C>GCA433058965TGFBR2c.978C>G (p.Ala326=)
n.2574C>G
c.1053C>G (p.Ala351=)
c.1005C>G (p.Ala335=)
c.930C>G (p.Ala310=)
c.873C>G (p.Ala291=)
3g.30672161C>TCA433058966TGFBR2c.978C>T (p.Ala326=)
n.2574C>T
c.1053C>T (p.Ala351=)
c.1005C>T (p.Ala335=)
c.930C>T (p.Ala310=)
c.873C>T (p.Ala291=)
 ClinVar dbSNP gnomAD v4
3g.30672162T>ACA351808293TGFBR2c.979T>A (p.Phe327Ile)
n.2575T>A
c.1054T>A (p.Phe352Ile)
c.1006T>A (p.Phe336Ile)
c.931T>A (p.Phe311Ile)
c.874T>A (p.Phe292Ile)
3g.30672162T>CCA351808294TGFBR2c.979T>C (p.Phe327Leu)
n.2575T>C
c.1054T>C (p.Phe352Leu)
c.1006T>C (p.Phe336Leu)
c.931T>C (p.Phe311Leu)
c.874T>C (p.Phe292Leu)
 gnomAD v4
3g.30672162T>GCA351808295TGFBR2c.979T>G (p.Phe327Val)
n.2575T>G
c.1054T>G (p.Phe352Val)
c.1006T>G (p.Phe336Val)
c.931T>G (p.Phe311Val)
c.874T>G (p.Phe292Val)
3g.30672163T>ACA351808296TGFBR2c.980T>A (p.Phe327Tyr)
n.2576T>A
c.1055T>A (p.Phe352Tyr)
c.1007T>A (p.Phe336Tyr)
c.932T>A (p.Phe311Tyr)
c.875T>A (p.Phe292Tyr)
3g.30672163T>CCA351808297TGFBR2c.980T>C (p.Phe327Ser)
n.2576T>C
c.1055T>C (p.Phe352Ser)
c.1007T>C (p.Phe336Ser)
c.932T>C (p.Phe311Ser)
c.875T>C (p.Phe292Ser)
3g.30672163T>GCA351808298TGFBR2c.980T>G (p.Phe327Cys)
n.2576T>G
c.1055T>G (p.Phe352Cys)
c.1007T>G (p.Phe336Cys)
c.932T>G (p.Phe311Cys)
c.875T>G (p.Phe292Cys)
3g.30672163_30672164insGATCAGCA2702371626TGFBR2c.980_981insGATCAG (p.Phe327delinsLeuIleSer)
n.2576_2577insGATCAG
c.1055_1056insGATCAG (p.Phe352delinsLeuIleSer)
c.1007_1008insGATCAG (p.Phe336delinsLeuIleSer)
c.932_933insGATCAG (p.Phe311delinsLeuIleSer)
c.875_876insGATCAG (p.Phe292delinsLeuIleSer)
 dbSNP
3g.30672164C>ACA351808299TGFBR2c.981C>A (p.Phe327Leu)
n.2577C>A
c.1056C>A (p.Phe352Leu)
c.1008C>A (p.Phe336Leu)
c.933C>A (p.Phe311Leu)
c.876C>A (p.Phe292Leu)
 dbSNP
3g.30672164C=CA1354873159TGFBR2c.981C= (p.Phe327=)
n.2577C=
c.1056C= (p.Phe352=)
c.1008C= (p.Phe336=)
c.933C= (p.Phe311=)
c.876C= (p.Phe292=)
3g.30672164C>GCA351808300TGFBR2c.981C>G (p.Phe327Leu)
n.2577C>G
c.1056C>G (p.Phe352Leu)
c.1008C>G (p.Phe336Leu)
c.933C>G (p.Phe311Leu)
c.876C>G (p.Phe292Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.30672164C>TCA433058967TGFBR2c.981C>T (p.Phe327=)
n.2577C>T
c.1056C>T (p.Phe352=)
c.1008C>T (p.Phe336=)
c.933C>T (p.Phe311=)
c.876C>T (p.Phe292=)
 dbSNP
3g.30672165C>ACA351808301TGFBR2c.982C>A (p.His328Asn)
n.2578C>A
c.1057C>A (p.His353Asn)
c.1009C>A (p.His337Asn)
c.934C>A (p.His312Asn)
c.877C>A (p.His293Asn)
 dbSNP
3g.30672165C>GCA351808302TGFBR2c.982C>G (p.His328Asp)
n.2578C>G
c.1057C>G (p.His353Asp)
c.1009C>G (p.His337Asp)
c.934C>G (p.His312Asp)
c.877C>G (p.His293Asp)
3g.30672165C>TCA351808303TGFBR2c.982C>T (p.His328Tyr)
n.2578C>T
c.1057C>T (p.His353Tyr)
c.1009C>T (p.His337Tyr)
c.934C>T (p.His312Tyr)
c.877C>T (p.His293Tyr)
 dbSNP COSMIC COSMIC
3g.30672166A>CCA351808305TGFBR2c.983A>C (p.His328Pro)
n.2579A>C
c.1058A>C (p.His353Pro)
c.1010A>C (p.His337Pro)
c.935A>C (p.His312Pro)
c.878A>C (p.His293Pro)
3g.30672166A>GCA351808306TGFBR2c.983A>G (p.His328Arg)
n.2579A>G
c.1058A>G (p.His353Arg)
c.1010A>G (p.His337Arg)
c.935A>G (p.His312Arg)
c.878A>G (p.His293Arg)
3g.30672166A>TCA351808304TGFBR2c.983A>T (p.His328Leu)
n.2579A>T
c.1058A>T (p.His353Leu)
c.1010A>T (p.His337Leu)
c.935A>T (p.His312Leu)
c.878A>T (p.His293Leu)
 dbSNP
3g.30672167C>ACA050726TGFBR2c.984C>A (p.His328Gln)
n.2580C>A
c.1059C>A (p.His353Gln)
c.1011C>A (p.His337Gln)
c.936C>A (p.His312Gln)
c.879C>A (p.His293Gln)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672167C=CA1354873160TGFBR2c.984C= (p.His328=)
n.2580C=
c.1059C= (p.His353=)
c.1011C= (p.His337=)
c.936C= (p.His312=)
c.879C= (p.His293=)
3g.30672167C>GCA351808307TGFBR2c.984C>G (p.His328Gln)
n.2580C>G
c.1059C>G (p.His353Gln)
c.1011C>G (p.His337Gln)
c.936C>G (p.His312Gln)
c.879C>G (p.His293Gln)
 dbSNP
3g.30672167C>TCA020559TGFBR2c.984C>T (p.His328=)
n.2580C>T
c.1059C>T (p.His353=)
c.1011C>T (p.His337=)
c.936C>T (p.His312=)
c.879C>T (p.His293=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.30672168G>ACA020563TGFBR2c.985G>A (p.Ala329Thr)
n.2581G>A
c.1060G>A (p.Ala354Thr)
c.1012G>A (p.Ala338Thr)
c.937G>A (p.Ala313Thr)
c.880G>A (p.Ala294Thr)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672168G>CCA351808308TGFBR2c.985G>C (p.Ala329Pro)
n.2581G>C
c.1060G>C (p.Ala354Pro)
c.1012G>C (p.Ala338Pro)
c.937G>C (p.Ala313Pro)
c.880G>C (p.Ala294Pro)
 dbSNP
3g.30672168G=CA1354873161TGFBR2c.985G= (p.Ala329=)
n.2581G=
c.1060G= (p.Ala354=)
c.1012G= (p.Ala338=)
c.937G= (p.Ala313=)
c.880G= (p.Ala294=)
3g.30672168G>TCA351808309TGFBR2c.985G>T (p.Ala329Ser)
n.2581G>T
c.1060G>T (p.Ala354Ser)
c.1012G>T (p.Ala338Ser)
c.937G>T (p.Ala313Ser)
c.880G>T (p.Ala294Ser)
3g.30672169C>ACA351808310TGFBR2c.986C>A (p.Ala329Asp)
n.2582C>A
c.1061C>A (p.Ala354Asp)
c.1013C>A (p.Ala338Asp)
c.938C>A (p.Ala313Asp)
c.881C>A (p.Ala294Asp)
 dbSNP
3g.30672169C=CA1354873162TGFBR2c.986C= (p.Ala329=)
n.2582C=
c.1061C= (p.Ala354=)
c.1013C= (p.Ala338=)
c.938C= (p.Ala313=)
c.881C= (p.Ala294=)
3g.30672169C>GCA351808311TGFBR2c.986C>G (p.Ala329Gly)
n.2582C>G
c.1061C>G (p.Ala354Gly)
c.1013C>G (p.Ala338Gly)
c.938C>G (p.Ala313Gly)
c.881C>G (p.Ala294Gly)
 dbSNP gnomAD v4
3g.30672169C>TCA050756TGFBR2c.986C>T (p.Ala329Val)
n.2582C>T
c.1061C>T (p.Ala354Val)
c.1013C>T (p.Ala338Val)
c.938C>T (p.Ala313Val)
c.881C>T (p.Ala294Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672170C>ACA433058969TGFBR2c.987C>A (p.Ala329=)
n.2583C>A
c.1062C>A (p.Ala354=)
c.1014C>A (p.Ala338=)
c.939C>A (p.Ala313=)
c.882C>A (p.Ala294=)
 dbSNP
3g.30672170C=CA1354873163TGFBR2c.987C= (p.Ala329=)
n.2583C=
c.1062C= (p.Ala354=)
c.1014C= (p.Ala338=)
c.939C= (p.Ala313=)
c.882C= (p.Ala294=)
3g.30672170C>GCA433058968TGFBR2c.987C>G (p.Ala329=)
n.2583C>G
c.1062C>G (p.Ala354=)
c.1014C>G (p.Ala338=)
c.939C>G (p.Ala313=)
c.882C>G (p.Ala294=)
3g.30672170C>TCA020567TGFBR2c.987C>T (p.Ala329=)
n.2583C>T
c.1062C>T (p.Ala354=)
c.1014C>T (p.Ala338=)
c.939C>T (p.Ala313=)
c.882C>T (p.Ala294=)
 ClinVar dbSNP
3g.30672171A>CCA351808312TGFBR2c.988A>C (p.Lys330Gln)
n.2584A>C
c.1063A>C (p.Lys355Gln)
c.1015A>C (p.Lys339Gln)
c.940A>C (p.Lys314Gln)
c.883A>C (p.Lys295Gln)
3g.30672171A>GCA351808313TGFBR2c.988A>G (p.Lys330Glu)
n.2584A>G
c.1063A>G (p.Lys355Glu)
c.1015A>G (p.Lys339Glu)
c.940A>G (p.Lys314Glu)
c.883A>G (p.Lys295Glu)
3g.30672171A>TCA351808314TGFBR2c.988A>T (p.Lys330Ter)
n.2584A>T
c.1063A>T (p.Lys355Ter)
c.1015A>T (p.Lys339Ter)
c.940A>T (p.Lys314Ter)
c.883A>T (p.Lys295Ter)
3g.30672172A>CCA351808317TGFBR2c.989A>C (p.Lys330Thr)
n.2585A>C
c.1064A>C (p.Lys355Thr)
c.1016A>C (p.Lys339Thr)
c.941A>C (p.Lys314Thr)
c.884A>C (p.Lys295Thr)
3g.30672172A>GCA351808315TGFBR2c.989A>G (p.Lys330Arg)
n.2585A>G
c.1064A>G (p.Lys355Arg)
c.1016A>G (p.Lys339Arg)
c.941A>G (p.Lys314Arg)
c.884A>G (p.Lys295Arg)
 dbSNP gnomAD v4
3g.30672172A>TCA351808316TGFBR2c.989A>T (p.Lys330Met)
n.2585A>T
c.1064A>T (p.Lys355Met)
c.1016A>T (p.Lys339Met)
c.941A>T (p.Lys314Met)
c.884A>T (p.Lys295Met)
 dbSNP
3g.30672173G>ACA433058970TGFBR2c.990G>A (p.Lys330=)
n.2586G>A
c.1065G>A (p.Lys355=)
c.1017G>A (p.Lys339=)
c.942G>A (p.Lys314=)
c.885G>A (p.Lys295=)
3g.30672173G>CCA351808318TGFBR2c.990G>C (p.Lys330Asn)
n.2586G>C
c.1065G>C (p.Lys355Asn)
c.1017G>C (p.Lys339Asn)
c.942G>C (p.Lys314Asn)
c.885G>C (p.Lys295Asn)
 dbSNP
3g.30672173G>TCA351808319TGFBR2c.990G>T (p.Lys330Asn)
n.2586G>T
c.1065G>T (p.Lys355Asn)
c.1017G>T (p.Lys339Asn)
c.942G>T (p.Lys314Asn)
c.885G>T (p.Lys295Asn)
3g.30672174G>ACA050772TGFBR2c.991G>A (p.Gly331Ser)
n.2587G>A
c.1066G>A (p.Gly356Ser)
c.1018G>A (p.Gly340Ser)
c.943G>A (p.Gly315Ser)
c.886G>A (p.Gly296Ser)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672174G>CCA351808320TGFBR2c.991G>C (p.Gly331Arg)
n.2587G>C
c.1066G>C (p.Gly356Arg)
c.1018G>C (p.Gly340Arg)
c.943G>C (p.Gly315Arg)
c.886G>C (p.Gly296Arg)
 dbSNP
3g.30672174G=CA1354873164TGFBR2c.991G= (p.Gly331=)
n.2587G=
c.1066G= (p.Gly356=)
c.1018G= (p.Gly340=)
c.943G= (p.Gly315=)
c.886G= (p.Gly296=)
3g.30672174G>TCA351808321TGFBR2c.991G>T (p.Gly331Cys)
n.2587G>T
c.1066G>T (p.Gly356Cys)
c.1018G>T (p.Gly340Cys)
c.943G>T (p.Gly315Cys)
c.886G>T (p.Gly296Cys)
 dbSNP
3g.30672175G>ACA351808322TGFBR2c.992G>A (p.Gly331Asp)
n.2588G>A
c.1067G>A (p.Gly356Asp)
c.1019G>A (p.Gly340Asp)
c.944G>A (p.Gly315Asp)
c.887G>A (p.Gly296Asp)
 dbSNP gnomAD v2 gnomAD v4
3g.30672175G>CCA351808323TGFBR2c.992G>C (p.Gly331Ala)
n.2588G>C
c.1067G>C (p.Gly356Ala)
c.1019G>C (p.Gly340Ala)
c.944G>C (p.Gly315Ala)
c.887G>C (p.Gly296Ala)
 dbSNP
3g.30672175G=CA1354873165TGFBR2c.992G= (p.Gly331=)
n.2588G=
c.1067G= (p.Gly356=)
c.1019G= (p.Gly340=)
c.944G= (p.Gly315=)
c.887G= (p.Gly296=)
3g.30672175G>TCA351808324TGFBR2c.992G>T (p.Gly331Val)
n.2588G>T
c.1067G>T (p.Gly356Val)
c.1019G>T (p.Gly340Val)
c.944G>T (p.Gly315Val)
c.887G>T (p.Gly296Val)
3g.30672176C>ACA433058971TGFBR2c.993C>A (p.Gly331=)
n.2589C>A
c.1068C>A (p.Gly356=)
c.1020C>A (p.Gly340=)
c.945C>A (p.Gly315=)
c.888C>A (p.Gly296=)
 dbSNP gnomAD v2 gnomAD v4
3g.30672176C=CA1354873166TGFBR2c.993C= (p.Gly331=)
n.2589C=
c.1068C= (p.Gly356=)
c.1020C= (p.Gly340=)
c.945C= (p.Gly315=)
c.888C= (p.Gly296=)
3g.30672176C>GCA433058973TGFBR2c.993C>G (p.Gly331=)
n.2589C>G
c.1068C>G (p.Gly356=)
c.1020C>G (p.Gly340=)
c.945C>G (p.Gly315=)
c.888C>G (p.Gly296=)
 dbSNP
3g.30672176C>TCA433058972TGFBR2c.993C>T (p.Gly331=)
n.2589C>T
c.1068C>T (p.Gly356=)
c.1020C>T (p.Gly340=)
c.945C>T (p.Gly315=)
c.888C>T (p.Gly296=)
 ClinVar dbSNP
3g.30672177A>CCA351808325TGFBR2c.994A>C (p.Asn332His)
n.2590A>C
c.1069A>C (p.Asn357His)
c.1021A>C (p.Asn341His)
c.946A>C (p.Asn316His)
c.889A>C (p.Asn297His)
3g.30672177A>GCA351808326TGFBR2c.994A>G (p.Asn332Asp)
n.2590A>G
c.1069A>G (p.Asn357Asp)
c.1021A>G (p.Asn341Asp)
c.946A>G (p.Asn316Asp)
c.889A>G (p.Asn297Asp)
3g.30672177A>TCA351808327TGFBR2c.994A>T (p.Asn332Tyr)
n.2590A>T
c.1069A>T (p.Asn357Tyr)
c.1021A>T (p.Asn341Tyr)
c.946A>T (p.Asn316Tyr)
c.889A>T (p.Asn297Tyr)
3g.30672178A>CCA351808328TGFBR2c.995A>C (p.Asn332Thr)
n.2591A>C
c.1070A>C (p.Asn357Thr)
c.1022A>C (p.Asn341Thr)
c.947A>C (p.Asn316Thr)
c.890A>C (p.Asn297Thr)
 dbSNP
3g.30672178A>GCA351808330TGFBR2c.995A>G (p.Asn332Ser)
n.2591A>G
c.1070A>G (p.Asn357Ser)
c.1022A>G (p.Asn341Ser)
c.947A>G (p.Asn316Ser)
c.890A>G (p.Asn297Ser)
 COSMIC COSMIC
3g.30672178A>TCA351808329TGFBR2c.995A>T (p.Asn332Ile)
n.2591A>T
c.1070A>T (p.Asn357Ile)
c.1022A>T (p.Asn341Ile)
c.947A>T (p.Asn316Ile)
c.890A>T (p.Asn297Ile)
 dbSNP
3g.30672179C>ACA351808331TGFBR2c.996C>A (p.Asn332Lys)
n.2592C>A
c.1071C>A (p.Asn357Lys)
c.1023C>A (p.Asn341Lys)
c.948C>A (p.Asn316Lys)
c.891C>A (p.Asn297Lys)
3g.30672179C>GCA351808332TGFBR2c.996C>G (p.Asn332Lys)
n.2592C>G
c.1071C>G (p.Asn357Lys)
c.1023C>G (p.Asn341Lys)
c.948C>G (p.Asn316Lys)
c.891C>G (p.Asn297Lys)
3g.30672179C>TCA433058974TGFBR2c.996C>T (p.Asn332=)
n.2592C>T
c.1071C>T (p.Asn357=)
c.1023C>T (p.Asn341=)
c.948C>T (p.Asn316=)
c.891C>T (p.Asn297=)
 ClinVar gnomAD v4
3g.30672180C>ACA351808333TGFBR2c.997C>A (p.Leu333Ile)
n.2593C>A
c.1072C>A (p.Leu358Ile)
c.1024C>A (p.Leu342Ile)
c.949C>A (p.Leu317Ile)
c.892C>A (p.Leu298Ile)
3g.30672180C=CA1354873167TGFBR2c.997C= (p.Leu333=)
n.2593C=
c.1072C= (p.Leu358=)
c.1024C= (p.Leu342=)
c.949C= (p.Leu317=)
c.892C= (p.Leu298=)
3g.30672180C>GCA351808334TGFBR2c.997C>G (p.Leu333Val)
n.2593C>G
c.1072C>G (p.Leu358Val)
c.1024C>G (p.Leu342Val)
c.949C>G (p.Leu317Val)
c.892C>G (p.Leu298Val)
 ClinVar dbSNP gnomAD v4
3g.30672180C>TCA433058975TGFBR2c.997C>T (p.Leu333=)
n.2593C>T
c.1072C>T (p.Leu358=)
c.1024C>T (p.Leu342=)
c.949C>T (p.Leu317=)
c.892C>T (p.Leu298=)
 gnomAD v4
3g.30672181T>ACA324102TGFBR2c.998T>A (p.Leu333Gln)
n.2594T>A
c.1073T>A (p.Leu358Gln)
c.1025T>A (p.Leu342Gln)
c.950T>A (p.Leu317Gln)
c.893T>A (p.Leu298Gln)
 ClinVar dbSNP
3g.30672181T>CCA351808336TGFBR2c.998T>C (p.Leu333Pro)
n.2594T>C
c.1073T>C (p.Leu358Pro)
c.1025T>C (p.Leu342Pro)
c.950T>C (p.Leu317Pro)
c.893T>C (p.Leu298Pro)
3g.30672181T>GCA351808335TGFBR2c.998T>G (p.Leu333Arg)
n.2594T>G
c.1073T>G (p.Leu358Arg)
c.1025T>G (p.Leu342Arg)
c.950T>G (p.Leu317Arg)
c.893T>G (p.Leu298Arg)
3g.30672181T=CA1354873168TGFBR2c.998T= (p.Leu333=)
n.2594T=
c.1073T= (p.Leu358=)
c.1025T= (p.Leu342=)
c.950T= (p.Leu317=)
c.893T= (p.Leu298=)
3g.30672182A=CA1354873169TGFBR2c.999A= (p.Leu333=)
n.2595A=
c.1074A= (p.Leu358=)
c.1026A= (p.Leu342=)
c.951A= (p.Leu317=)
c.894A= (p.Leu298=)
3g.30672182A>CCA433058977TGFBR2c.999A>C (p.Leu333=)
n.2595A>C
c.1074A>C (p.Leu358=)
c.1026A>C (p.Leu342=)
c.951A>C (p.Leu317=)
c.894A>C (p.Leu298=)
3g.30672182A>GCA020571TGFBR2c.999A>G (p.Leu333=)
n.2595A>G
c.1074A>G (p.Leu358=)
c.1026A>G (p.Leu342=)
c.951A>G (p.Leu317=)
c.894A>G (p.Leu298=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672182A>TCA433058978TGFBR2c.999A>T (p.Leu333=)
n.2595A>T
c.1074A>T (p.Leu358=)
c.1026A>T (p.Leu342=)
c.951A>T (p.Leu317=)
c.894A>T (p.Leu298=)
3g.30672183C>ACA351808337TGFBR2c.1000C>A (p.Gln334Lys)
n.2596C>A
c.1075C>A (p.Gln359Lys)
c.1027C>A (p.Gln343Lys)
c.952C>A (p.Gln318Lys)
c.895C>A (p.Gln299Lys)
3g.30672183C>GCA351808338TGFBR2c.1000C>G (p.Gln334Glu)
n.2596C>G
c.1075C>G (p.Gln359Glu)
c.1027C>G (p.Gln343Glu)
c.952C>G (p.Gln318Glu)
c.895C>G (p.Gln299Glu)
 dbSNP
3g.30672183C>TCA351808339TGFBR2c.1000C>T (p.Gln334Ter)
n.2596C>T
c.1075C>T (p.Gln359Ter)
c.1027C>T (p.Gln343Ter)
c.952C>T (p.Gln318Ter)
c.895C>T (p.Gln299Ter)
3g.30672184A=CA1354873170TGFBR2c.1001A= (p.Gln334=)
n.2597A=
c.1076A= (p.Gln359=)
c.1028A= (p.Gln343=)
c.953A= (p.Gln318=)
c.896A= (p.Gln299=)
3g.30672184A>CCA351808340TGFBR2c.1001A>C (p.Gln334Pro)
n.2597A>C
c.1076A>C (p.Gln359Pro)
c.1028A>C (p.Gln343Pro)
c.953A>C (p.Gln318Pro)
c.896A>C (p.Gln299Pro)
3g.30672184A>GCA045319TGFBR2c.1001A>G (p.Gln334Arg)
n.2597A>G
c.1076A>G (p.Gln359Arg)
c.1028A>G (p.Gln343Arg)
c.953A>G (p.Gln318Arg)
c.896A>G (p.Gln299Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672184A>TCA351808341TGFBR2c.1001A>T (p.Gln334Leu)
n.2597A>T
c.1076A>T (p.Gln359Leu)
c.1028A>T (p.Gln343Leu)
c.953A>T (p.Gln318Leu)
c.896A>T (p.Gln299Leu)
 dbSNP gnomAD v2 gnomAD v4
3g.30672185G>ACA433058979TGFBR2c.1002G>A (p.Gln334=)
n.2598G>A
c.1077G>A (p.Gln359=)
c.1029G>A (p.Gln343=)
c.954G>A (p.Gln318=)
c.897G>A (p.Gln299=)
 gnomAD v4
3g.30672185G>CCA351808342TGFBR2c.1002G>C (p.Gln334His)
n.2598G>C
c.1077G>C (p.Gln359His)
c.1029G>C (p.Gln343His)
c.954G>C (p.Gln318His)
c.897G>C (p.Gln299His)
3g.30672185G=CA1354873171TGFBR2c.1002G= (p.Gln334=)
n.2598G=
c.1077G= (p.Gln359=)
c.1029G= (p.Gln343=)
c.954G= (p.Gln318=)
c.897G= (p.Gln299=)
3g.30672185G>TCA351808343TGFBR2c.1002G>T (p.Gln334His)
n.2598G>T
c.1077G>T (p.Gln359His)
c.1029G>T (p.Gln343His)
c.954G>T (p.Gln318His)
c.897G>T (p.Gln299His)
 ClinVar dbSNP

Number of alleles fetched