Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.30672188G>ACA433058981TGFBR2c.1005G>A (p.Glu335=)
n.2601G>A
c.1080G>A (p.Glu360=)
c.1032G>A (p.Glu344=)
c.957G>A (p.Glu319=)
c.900G>A (p.Glu300=)
 dbSNP
3g.30672188G>CCA351808349TGFBR2c.1005G>C (p.Glu335Asp)
n.2601G>C
c.1080G>C (p.Glu360Asp)
c.1032G>C (p.Glu344Asp)
c.957G>C (p.Glu319Asp)
c.900G>C (p.Glu300Asp)
3g.30672188G>TCA351808350TGFBR2c.1005G>T (p.Glu335Asp)
n.2601G>T
c.1080G>T (p.Glu360Asp)
c.1032G>T (p.Glu344Asp)
c.957G>T (p.Glu319Asp)
c.900G>T (p.Glu300Asp)
3g.30672189T>ACA020575TGFBR2c.1006T>A (p.Tyr336Asn)
n.2602T>A
c.1081T>A (p.Tyr361Asn)
c.1033T>A (p.Tyr345Asn)
c.958T>A (p.Tyr320Asn)
c.901T>A (p.Tyr301Asn)
 ClinVar dbSNP
3g.30672189T>CCA351808351TGFBR2c.1006T>C (p.Tyr336His)
n.2602T>C
c.1081T>C (p.Tyr361His)
c.1033T>C (p.Tyr345His)
c.958T>C (p.Tyr320His)
c.901T>C (p.Tyr301His)
3g.30672189T>GCA351808352TGFBR2c.1006T>G (p.Tyr336Asp)
n.2602T>G
c.1081T>G (p.Tyr361Asp)
c.1033T>G (p.Tyr345Asp)
c.958T>G (p.Tyr320Asp)
c.901T>G (p.Tyr301Asp)
 ClinVar dbSNP
3g.30672189T=CA1354873173TGFBR2c.1006T= (p.Tyr336=)
n.2602T=
c.1081T= (p.Tyr361=)
c.1033T= (p.Tyr345=)
c.958T= (p.Tyr320=)
c.901T= (p.Tyr301=)
3g.30672190A=CA1354873174TGFBR2c.1007A= (p.Tyr336=)
n.2603A=
c.1082A= (p.Tyr361=)
c.1034A= (p.Tyr345=)
c.959A= (p.Tyr320=)
c.902A= (p.Tyr301=)
3g.30672190A>CCA351808353TGFBR2c.1007A>C (p.Tyr336Ser)
n.2603A>C
c.1082A>C (p.Tyr361Ser)
c.1034A>C (p.Tyr345Ser)
c.959A>C (p.Tyr320Ser)
c.902A>C (p.Tyr301Ser)
 ClinVar
3g.30672190A>GCA351808354TGFBR2c.1007A>G (p.Tyr336Cys)
n.2603A>G
c.1082A>G (p.Tyr361Cys)
c.1034A>G (p.Tyr345Cys)
c.959A>G (p.Tyr320Cys)
c.902A>G (p.Tyr301Cys)
3g.30672190A>TCA351808355TGFBR2c.1007A>T (p.Tyr336Phe)
n.2603A>T
c.1082A>T (p.Tyr361Phe)
c.1034A>T (p.Tyr345Phe)
c.959A>T (p.Tyr320Phe)
c.902A>T (p.Tyr301Phe)
 ClinVar dbSNP gnomAD v4
3g.30672191C>ACA351808356TGFBR2c.1008C>A (p.Tyr336Ter)
n.2604C>A
c.1083C>A (p.Tyr361Ter)
c.1035C>A (p.Tyr345Ter)
c.960C>A (p.Tyr320Ter)
c.903C>A (p.Tyr301Ter)
3g.30672191C=CA1354873175TGFBR2c.1008C= (p.Tyr336=)
n.2604C=
c.1083C= (p.Tyr361=)
c.1035C= (p.Tyr345=)
c.960C= (p.Tyr320=)
c.903C= (p.Tyr301=)
3g.30672191C>GCA351808357TGFBR2c.1008C>G (p.Tyr336Ter)
n.2604C>G
c.1083C>G (p.Tyr361Ter)
c.1035C>G (p.Tyr345Ter)
c.960C>G (p.Tyr320Ter)
c.903C>G (p.Tyr301Ter)
3g.30672191C>TCA045334TGFBR2c.1008C>T (p.Tyr336=)
n.2604C>T
c.1083C>T (p.Tyr361=)
c.1035C>T (p.Tyr345=)
c.960C>T (p.Tyr320=)
c.903C>T (p.Tyr301=)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672192C>ACA351808358TGFBR2c.1009C>A (p.Leu337Met)
n.2605C>A
c.1084C>A (p.Leu362Met)
c.1036C>A (p.Leu346Met)
c.961C>A (p.Leu321Met)
c.904C>A (p.Leu302Met)
3g.30672192C>GCA351808359TGFBR2c.1009C>G (p.Leu337Val)
n.2605C>G
c.1084C>G (p.Leu362Val)
c.1036C>G (p.Leu346Val)
c.961C>G (p.Leu321Val)
c.904C>G (p.Leu302Val)
3g.30672192C>TCA433058987TGFBR2c.1009C>T (p.Leu337=)
n.2605C>T
c.1084C>T (p.Leu362=)
c.1036C>T (p.Leu346=)
c.961C>T (p.Leu321=)
c.904C>T (p.Leu302=)
 dbSNP
3g.30672193T>ACA351808360TGFBR2c.1010T>A (p.Leu337Gln)
n.2606T>A
c.1085T>A (p.Leu362Gln)
c.1037T>A (p.Leu346Gln)
c.962T>A (p.Leu321Gln)
c.905T>A (p.Leu302Gln)
3g.30672193T>CCA351808361TGFBR2c.1010T>C (p.Leu337Pro)
n.2606T>C
c.1085T>C (p.Leu362Pro)
c.1037T>C (p.Leu346Pro)
c.962T>C (p.Leu321Pro)
c.905T>C (p.Leu302Pro)
3g.30672193T>GCA351808362TGFBR2c.1010T>G (p.Leu337Arg)
n.2606T>G
c.1085T>G (p.Leu362Arg)
c.1037T>G (p.Leu346Arg)
c.962T>G (p.Leu321Arg)
c.905T>G (p.Leu302Arg)
3g.30672194G>ACA433058988TGFBR2c.1011G>A (p.Leu337=)
n.2607G>A
c.1086G>A (p.Leu362=)
c.1038G>A (p.Leu346=)
c.963G>A (p.Leu321=)
c.906G>A (p.Leu302=)
3g.30672194G>CCA433058989TGFBR2c.1011G>C (p.Leu337=)
n.2607G>C
c.1086G>C (p.Leu362=)
c.1038G>C (p.Leu346=)
c.963G>C (p.Leu321=)
c.906G>C (p.Leu302=)
3g.30672194G>TCA433058990TGFBR2c.1011G>T (p.Leu337=)
n.2607G>T
c.1086G>T (p.Leu362=)
c.1038G>T (p.Leu346=)
c.963G>T (p.Leu321=)
c.906G>T (p.Leu302=)
3g.30672195A>CCA351808363TGFBR2c.1012A>C (p.Thr338Pro)
n.2608A>C
c.1087A>C (p.Thr363Pro)
c.1039A>C (p.Thr347Pro)
c.964A>C (p.Thr322Pro)
c.907A>C (p.Thr303Pro)
3g.30672195A>GCA351808364TGFBR2c.1012A>G (p.Thr338Ala)
n.2608A>G
c.1087A>G (p.Thr363Ala)
c.1039A>G (p.Thr347Ala)
c.964A>G (p.Thr322Ala)
c.907A>G (p.Thr303Ala)
3g.30672195A>TCA351808365TGFBR2c.1012A>T (p.Thr338Ser)
n.2608A>T
c.1087A>T (p.Thr363Ser)
c.1039A>T (p.Thr347Ser)
c.964A>T (p.Thr322Ser)
c.907A>T (p.Thr303Ser)
3g.30672196C>ACA71528554TGFBR2c.1013C>A (p.Thr338Lys)
n.2609C>A
c.1088C>A (p.Thr363Lys)
c.1040C>A (p.Thr347Lys)
c.965C>A (p.Thr322Lys)
c.908C>A (p.Thr303Lys)
 ClinVar dbSNP gnomAD v4
3g.30672196C=CA1354873176TGFBR2c.1013C= (p.Thr338=)
n.2609C=
c.1088C= (p.Thr363=)
c.1040C= (p.Thr347=)
c.965C= (p.Thr322=)
c.908C= (p.Thr303=)
3g.30672196C>GCA351808366TGFBR2c.1013C>G (p.Thr338Arg)
n.2609C>G
c.1088C>G (p.Thr363Arg)
c.1040C>G (p.Thr347Arg)
c.965C>G (p.Thr322Arg)
c.908C>G (p.Thr303Arg)
 dbSNP gnomAD v4
3g.30672196C>TCA71528567TGFBR2c.1013C>T (p.Thr338Met)
n.2609C>T
c.1088C>T (p.Thr363Met)
c.1040C>T (p.Thr347Met)
c.965C>T (p.Thr322Met)
c.908C>T (p.Thr303Met)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672197G>ACA045348TGFBR2c.1014G>A (p.Thr338=)
n.2610G>A
c.1089G>A (p.Thr363=)
c.1041G>A (p.Thr347=)
c.966G>A (p.Thr322=)
c.909G>A (p.Thr303=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672197G>CCA433058991TGFBR2c.1014G>C (p.Thr338=)
n.2610G>C
c.1089G>C (p.Thr363=)
c.1041G>C (p.Thr347=)
c.966G>C (p.Thr322=)
c.909G>C (p.Thr303=)
 ClinVar dbSNP gnomAD v4
3g.30672197G=CA1354873177TGFBR2c.1014G= (p.Thr338=)
n.2610G=
c.1089G= (p.Thr363=)
c.1041G= (p.Thr347=)
c.966G= (p.Thr322=)
c.909G= (p.Thr303=)
3g.30672197G>TCA045362TGFBR2c.1014G>T (p.Thr338=)
n.2610G>T
c.1089G>T (p.Thr363=)
c.1041G>T (p.Thr347=)
c.966G>T (p.Thr322=)
c.909G>T (p.Thr303=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672198C>ACA71528585TGFBR2c.1015C>A (p.Arg339=)
n.2611C>A
c.1090C>A (p.Arg364=)
c.1042C>A (p.Arg348=)
c.967C>A (p.Arg323=)
c.910C>A (p.Arg304=)
 dbSNP
3g.30672198C=CA1354873178TGFBR2c.1015C= (p.Arg339=)
n.2611C=
c.1090C= (p.Arg364=)
c.1042C= (p.Arg348=)
c.967C= (p.Arg323=)
c.910C= (p.Arg304=)
3g.30672198C>GCA351808367TGFBR2c.1015C>G (p.Arg339Gly)
n.2611C>G
c.1090C>G (p.Arg364Gly)
c.1042C>G (p.Arg348Gly)
c.967C>G (p.Arg323Gly)
c.910C>G (p.Arg304Gly)
 gnomAD v4
3g.30672198C>TCA045395TGFBR2c.1015C>T (p.Arg339Trp)
n.2611C>T
c.1090C>T (p.Arg364Trp)
c.1042C>T (p.Arg348Trp)
c.967C>T (p.Arg323Trp)
c.910C>T (p.Arg304Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672199G>ACA045405TGFBR2c.1016G>A (p.Arg339Gln)
n.2612G>A
c.1091G>A (p.Arg364Gln)
c.1043G>A (p.Arg348Gln)
c.968G>A (p.Arg323Gln)
c.911G>A (p.Arg304Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672199G>CCA020579TGFBR2c.1016G>C (p.Arg339Pro)
n.2612G>C
c.1091G>C (p.Arg364Pro)
c.1043G>C (p.Arg348Pro)
c.968G>C (p.Arg323Pro)
c.911G>C (p.Arg304Pro)
 ClinVar dbSNP
3g.30672199G=CA1354873179TGFBR2c.1016G= (p.Arg339=)
n.2612G=
c.1091G= (p.Arg364=)
c.1043G= (p.Arg348=)
c.968G= (p.Arg323=)
c.911G= (p.Arg304=)
3g.30672199G>TCA323392TGFBR2c.1016G>T (p.Arg339Leu)
n.2612G>T
c.1091G>T (p.Arg364Leu)
c.1043G>T (p.Arg348Leu)
c.968G>T (p.Arg323Leu)
c.911G>T (p.Arg304Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
3g.30672200G>ACA433058995TGFBR2c.1017G>A (p.Arg339=)
n.2613G>A
c.1092G>A (p.Arg364=)
c.1044G>A (p.Arg348=)
c.969G>A (p.Arg323=)
c.912G>A (p.Arg304=)
 dbSNP COSMIC
3g.30672200G>CCA433058997TGFBR2c.1017G>C (p.Arg339=)
n.2613G>C
c.1092G>C (p.Arg364=)
c.1044G>C (p.Arg348=)
c.969G>C (p.Arg323=)
c.912G>C (p.Arg304=)
 dbSNP
3g.30672200G=CA1354873180TGFBR2c.1017G= (p.Arg339=)
n.2613G=
c.1092G= (p.Arg364=)
c.1044G= (p.Arg348=)
c.969G= (p.Arg323=)
c.912G= (p.Arg304=)
3g.30672200G>TCA433058999TGFBR2c.1017G>T (p.Arg339=)
n.2613G>T
c.1092G>T (p.Arg364=)
c.1044G>T (p.Arg348=)
c.969G>T (p.Arg323=)
c.912G>T (p.Arg304=)
 dbSNP
3g.30672201C>ACA351808368TGFBR2c.1018C>A (p.His340Asn)
n.2614C>A
c.1093C>A (p.His365Asn)
c.1045C>A (p.His349Asn)
c.970C>A (p.His324Asn)
c.913C>A (p.His305Asn)
3g.30672201C>GCA351808369TGFBR2c.1018C>G (p.His340Asp)
n.2614C>G
c.1093C>G (p.His365Asp)
c.1045C>G (p.His349Asp)
c.970C>G (p.His324Asp)
c.913C>G (p.His305Asp)
3g.30672201C>TCA351808370TGFBR2c.1018C>T (p.His340Tyr)
n.2614C>T
c.1093C>T (p.His365Tyr)
c.1045C>T (p.His349Tyr)
c.970C>T (p.His324Tyr)
c.913C>T (p.His305Tyr)
 dbSNP
3g.30672202A=CA1354873181TGFBR2c.1019A= (p.His340=)
n.2615A=
c.1094A= (p.His365=)
c.1046A= (p.His349=)
c.971A= (p.His324=)
c.914A= (p.His305=)
3g.30672202A>CCA351808371TGFBR2c.1019A>C (p.His340Pro)
n.2615A>C
c.1094A>C (p.His365Pro)
c.1046A>C (p.His349Pro)
c.971A>C (p.His324Pro)
c.914A>C (p.His305Pro)
3g.30672202A>GCA351808372TGFBR2c.1019A>G (p.His340Arg)
n.2615A>G
c.1094A>G (p.His365Arg)
c.1046A>G (p.His349Arg)
c.971A>G (p.His324Arg)
c.914A>G (p.His305Arg)
 dbSNP gnomAD v3 gnomAD v4
3g.30672202A>TCA351808373TGFBR2c.1019A>T (p.His340Leu)
n.2615A>T
c.1094A>T (p.His365Leu)
c.1046A>T (p.His349Leu)
c.971A>T (p.His324Leu)
c.914A>T (p.His305Leu)
3g.30672203T>ACA351808374TGFBR2c.1020T>A (p.His340Gln)
n.2616T>A
c.1095T>A (p.His365Gln)
c.1047T>A (p.His349Gln)
c.972T>A (p.His324Gln)
c.915T>A (p.His305Gln)
3g.30672203T>CCA433059003TGFBR2c.1020T>C (p.His340=)
n.2616T>C
c.1095T>C (p.His365=)
c.1047T>C (p.His349=)
c.972T>C (p.His324=)
c.915T>C (p.His305=)
 dbSNP gnomAD v2 gnomAD v4
3g.30672203T>GCA351808375TGFBR2c.1020T>G (p.His340Gln)
n.2616T>G
c.1095T>G (p.His365Gln)
c.1047T>G (p.His349Gln)
c.972T>G (p.His324Gln)
c.915T>G (p.His305Gln)
3g.30672203T=CA1354873182TGFBR2c.1020T= (p.His340=)
n.2616T=
c.1095T= (p.His365=)
c.1047T= (p.His349=)
c.972T= (p.His324=)
c.915T= (p.His305=)
3g.30672204G>ACA351808376TGFBR2c.1021G>A (p.Val341Ile)
n.2617G>A
c.1096G>A (p.Val366Ile)
c.1048G>A (p.Val350Ile)
c.973G>A (p.Val325Ile)
c.916G>A (p.Val306Ile)
 dbSNP
3g.30672204G>CCA351808377TGFBR2c.1021G>C (p.Val341Leu)
n.2617G>C
c.1096G>C (p.Val366Leu)
c.1048G>C (p.Val350Leu)
c.973G>C (p.Val325Leu)
c.916G>C (p.Val306Leu)
 ClinVar
3g.30672204G>TCA351808378TGFBR2c.1021G>T (p.Val341Phe)
n.2617G>T
c.1096G>T (p.Val366Phe)
c.1048G>T (p.Val350Phe)
c.973G>T (p.Val325Phe)
c.916G>T (p.Val306Phe)
3g.30672205T>ACA351808381TGFBR2c.1022T>A (p.Val341Asp)
n.2618T>A
c.1097T>A (p.Val366Asp)
c.1049T>A (p.Val350Asp)
c.974T>A (p.Val325Asp)
c.917T>A (p.Val306Asp)
 dbSNP
3g.30672205T>CCA351808380TGFBR2c.1022T>C (p.Val341Ala)
n.2618T>C
c.1097T>C (p.Val366Ala)
c.1049T>C (p.Val350Ala)
c.974T>C (p.Val325Ala)
c.917T>C (p.Val306Ala)
3g.30672205T>GCA351808379TGFBR2c.1022T>G (p.Val341Gly)
n.2618T>G
c.1097T>G (p.Val366Gly)
c.1049T>G (p.Val350Gly)
c.974T>G (p.Val325Gly)
c.917T>G (p.Val306Gly)
 dbSNP
3g.30672206C>ACA433059005TGFBR2c.1023C>A (p.Val341=)
n.2619C>A
c.1098C>A (p.Val366=)
c.1050C>A (p.Val350=)
c.975C>A (p.Val325=)
c.918C>A (p.Val306=)
 dbSNP
3g.30672206C>GCA433059006TGFBR2c.1023C>G (p.Val341=)
n.2619C>G
c.1098C>G (p.Val366=)
c.1050C>G (p.Val350=)
c.975C>G (p.Val325=)
c.918C>G (p.Val306=)
3g.30672206C>TCA433059007TGFBR2c.1023C>T (p.Val341=)
n.2619C>T
c.1098C>T (p.Val366=)
c.1050C>T (p.Val350=)
c.975C>T (p.Val325=)
c.918C>T (p.Val306=)
 dbSNP gnomAD v4
3g.30672207A=CA1354873183TGFBR2c.1024A= (p.Ile342=)
n.2620A=
c.1099A= (p.Ile367=)
c.1051A= (p.Ile351=)
c.976A= (p.Ile326=)
c.919A= (p.Ile307=)
3g.30672207A>CCA351808382TGFBR2c.1024A>C (p.Ile342Leu)
n.2620A>C
c.1099A>C (p.Ile367Leu)
c.1051A>C (p.Ile351Leu)
c.976A>C (p.Ile326Leu)
c.919A>C (p.Ile307Leu)
3g.30672207A>GCA351808383TGFBR2c.1024A>G (p.Ile342Val)
n.2620A>G
c.1099A>G (p.Ile367Val)
c.1051A>G (p.Ile351Val)
c.976A>G (p.Ile326Val)
c.919A>G (p.Ile307Val)
3g.30672207A>TCA045424TGFBR2c.1024A>T (p.Ile342Phe)
n.2620A>T
c.1099A>T (p.Ile367Phe)
c.1051A>T (p.Ile351Phe)
c.976A>T (p.Ile326Phe)
c.919A>T (p.Ile307Phe)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672207dupCA2586965654TGFBR2c.1024dup (p.Ile342AsnfsTer23)
n.2620dup
c.1099dup (p.Ile367AsnfsTer23)
c.1051dup (p.Ile351AsnfsTer23)
c.976dup (p.Ile326AsnfsTer23)
c.919dup (p.Ile307AsnfsTer23)
3g.30672208T>ACA351808384TGFBR2c.1025T>A (p.Ile342Asn)
n.2621T>A
c.1100T>A (p.Ile367Asn)
c.1052T>A (p.Ile351Asn)
c.977T>A (p.Ile326Asn)
c.920T>A (p.Ile307Asn)
3g.30672208T>CCA351808385TGFBR2c.1025T>C (p.Ile342Thr)
n.2621T>C
c.1100T>C (p.Ile367Thr)
c.1052T>C (p.Ile351Thr)
c.977T>C (p.Ile326Thr)
c.920T>C (p.Ile307Thr)
3g.30672208T>GCA351808386TGFBR2c.1025T>G (p.Ile342Ser)
n.2621T>G
c.1100T>G (p.Ile367Ser)
c.1052T>G (p.Ile351Ser)
c.977T>G (p.Ile326Ser)
c.920T>G (p.Ile307Ser)
3g.30672209C>ACA433059009TGFBR2c.1026C>A (p.Ile342=)
n.2622C>A
c.1101C>A (p.Ile367=)
c.1053C>A (p.Ile351=)
c.978C>A (p.Ile326=)
c.921C>A (p.Ile307=)
 dbSNP
3g.30672209C>GCA351808387TGFBR2c.1026C>G (p.Ile342Met)
n.2622C>G
c.1101C>G (p.Ile367Met)
c.1053C>G (p.Ile351Met)
c.978C>G (p.Ile326Met)
c.921C>G (p.Ile307Met)
3g.30672209C>TCA433059010TGFBR2c.1026C>T (p.Ile342=)
n.2622C>T
c.1101C>T (p.Ile367=)
c.1053C>T (p.Ile351=)
c.978C>T (p.Ile326=)
c.921C>T (p.Ile307=)
3g.30672210A=CA1354873184TGFBR2c.1027A= (p.Ser343=)
n.2623A=
c.1102A= (p.Ser368=)
c.1054A= (p.Ser352=)
c.979A= (p.Ser327=)
c.922A= (p.Ser308=)
3g.30672210A>CCA351808388TGFBR2c.1027A>C (p.Ser343Arg)
n.2623A>C
c.1102A>C (p.Ser368Arg)
c.1054A>C (p.Ser352Arg)
c.979A>C (p.Ser327Arg)
c.922A>C (p.Ser308Arg)
3g.30672210A>GCA045437TGFBR2c.1027A>G (p.Ser343Gly)
n.2623A>G
c.1102A>G (p.Ser368Gly)
c.1054A>G (p.Ser352Gly)
c.979A>G (p.Ser327Gly)
c.922A>G (p.Ser308Gly)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672210A>TCA351808389TGFBR2c.1027A>T (p.Ser343Cys)
n.2623A>T
c.1102A>T (p.Ser368Cys)
c.1054A>T (p.Ser352Cys)
c.979A>T (p.Ser327Cys)
c.922A>T (p.Ser308Cys)
3g.30672211G>ACA351808390TGFBR2c.1028G>A (p.Ser343Asn)
n.2624G>A
c.1103G>A (p.Ser368Asn)
c.1055G>A (p.Ser352Asn)
c.980G>A (p.Ser327Asn)
c.923G>A (p.Ser308Asn)
 dbSNP
3g.30672211G>CCA351808391TGFBR2c.1028G>C (p.Ser343Thr)
n.2624G>C
c.1103G>C (p.Ser368Thr)
c.1055G>C (p.Ser352Thr)
c.980G>C (p.Ser327Thr)
c.923G>C (p.Ser308Thr)
3g.30672211G=CA1354873185TGFBR2c.1028G= (p.Ser343=)
n.2624G=
c.1103G= (p.Ser368=)
c.1055G= (p.Ser352=)
c.980G= (p.Ser327=)
c.923G= (p.Ser308=)
3g.30672211G>TCA351808392TGFBR2c.1028G>T (p.Ser343Ile)
n.2624G>T
c.1103G>T (p.Ser368Ile)
c.1055G>T (p.Ser352Ile)
c.980G>T (p.Ser327Ile)
c.923G>T (p.Ser308Ile)
 dbSNP
3g.30672212C>ACA351808393TGFBR2c.1029C>A (p.Ser343Arg)
n.2625C>A
c.1104C>A (p.Ser368Arg)
c.1056C>A (p.Ser352Arg)
c.981C>A (p.Ser327Arg)
c.924C>A (p.Ser308Arg)
3g.30672212C=CA1354873186TGFBR2c.1029C= (p.Ser343=)
n.2625C=
c.1104C= (p.Ser368=)
c.1056C= (p.Ser352=)
c.981C= (p.Ser327=)
c.924C= (p.Ser308=)
3g.30672212C>GCA351808394TGFBR2c.1029C>G (p.Ser343Arg)
n.2625C>G
c.1104C>G (p.Ser368Arg)
c.1056C>G (p.Ser352Arg)
c.981C>G (p.Ser327Arg)
c.924C>G (p.Ser308Arg)
3g.30672212C>TCA16611183TGFBR2c.1029C>T (p.Ser343=)
n.2625C>T
c.1104C>T (p.Ser368=)
c.1056C>T (p.Ser352=)
c.981C>T (p.Ser327=)
c.924C>T (p.Ser308=)
 ClinVar dbSNP
3g.30672213T>ACA351808395TGFBR2c.1030T>A (p.Trp344Arg)
n.2626T>A
c.1105T>A (p.Trp369Arg)
c.1057T>A (p.Trp353Arg)
c.982T>A (p.Trp328Arg)
c.925T>A (p.Trp309Arg)
3g.30672213T>CCA351808397TGFBR2c.1030T>C (p.Trp344Arg)
n.2626T>C
c.1105T>C (p.Trp369Arg)
c.1057T>C (p.Trp353Arg)
c.982T>C (p.Trp328Arg)
c.925T>C (p.Trp309Arg)
3g.30672213T>GCA351808396TGFBR2c.1030T>G (p.Trp344Gly)
n.2626T>G
c.1105T>G (p.Trp369Gly)
c.1057T>G (p.Trp353Gly)
c.982T>G (p.Trp328Gly)
c.925T>G (p.Trp309Gly)
3g.30672213_30672219delinsTGGGAGGCA1354873187TGFBR2c.1030_1036delinsTGGGAGG (p.Trp344=)
n.2626_2632delinsTGGGAGG
c.1105_1111delinsTGGGAGG (p.Trp369=)
c.1057_1063delinsTGGGAGG (p.Trp353=)
c.982_988delinsTGGGAGG (p.Trp328=)
c.925_931delinsTGGGAGG (p.Trp309=)
3g.30672214G>ACA351808398TGFBR2c.1031G>A (p.Trp344Ter)
n.2627G>A
c.1106G>A (p.Trp369Ter)
c.1058G>A (p.Trp353Ter)
c.983G>A (p.Trp328Ter)
c.926G>A (p.Trp309Ter)
3g.30672214G>CCA351808399TGFBR2c.1031G>C (p.Trp344Ser)
n.2627G>C
c.1106G>C (p.Trp369Ser)
c.1058G>C (p.Trp353Ser)
c.983G>C (p.Trp328Ser)
c.926G>C (p.Trp309Ser)
3g.30672214G>TCA351808400TGFBR2c.1031G>T (p.Trp344Leu)
n.2627G>T
c.1106G>T (p.Trp369Leu)
c.1058G>T (p.Trp353Leu)
c.983G>T (p.Trp328Leu)
c.926G>T (p.Trp309Leu)
3g.30672214_30672219delCA1046447381TGFBR2c.1031_1036del (p.Trp344_Asp346delinsTyr)
n.2627_2632del
c.1106_1111del (p.Trp369_Asp371delinsTyr)
c.1058_1063del (p.Trp353_Asp355delinsTyr)
c.983_988del (p.Trp328_Asp330delinsTyr)
c.926_931del (p.Trp309_Asp311delinsTyr)
 dbSNP gnomAD v3 gnomAD v4
3g.30672215_30672219delCA923726384TGFBR2c.1032_1036del (p.Trp344Ter)
n.2628_2632del
c.1107_1111del (p.Trp369Ter)
c.1059_1063del (p.Trp353Ter)
c.984_988del (p.Trp328Ter)
c.927_931del (p.Trp309Ter)
3g.30672215G>ACA351808401TGFBR2c.1032G>A (p.Trp344Ter)
n.2628G>A
c.1107G>A (p.Trp369Ter)
c.1059G>A (p.Trp353Ter)
c.984G>A (p.Trp328Ter)
c.927G>A (p.Trp309Ter)
 ClinVar gnomAD v4
3g.30672215G>CCA351808402TGFBR2c.1032G>C (p.Trp344Cys)
n.2628G>C
c.1107G>C (p.Trp369Cys)
c.1059G>C (p.Trp353Cys)
c.984G>C (p.Trp328Cys)
c.927G>C (p.Trp309Cys)
3g.30672215G>TCA351808403TGFBR2c.1032G>T (p.Trp344Cys)
n.2628G>T
c.1107G>T (p.Trp369Cys)
c.1059G>T (p.Trp353Cys)
c.984G>T (p.Trp328Cys)
c.927G>T (p.Trp309Cys)
3g.30672216G>ACA351808404TGFBR2c.1033G>A (p.Glu345Lys)
n.2629G>A
c.1108G>A (p.Glu370Lys)
c.1060G>A (p.Glu354Lys)
c.985G>A (p.Glu329Lys)
c.928G>A (p.Glu310Lys)
 dbSNP
3g.30672216G>CCA351808405TGFBR2c.1033G>C (p.Glu345Gln)
n.2629G>C
c.1108G>C (p.Glu370Gln)
c.1060G>C (p.Glu354Gln)
c.985G>C (p.Glu329Gln)
c.928G>C (p.Glu310Gln)
3g.30672216G>TCA351808406TGFBR2c.1033G>T (p.Glu345Ter)
n.2629G>T
c.1108G>T (p.Glu370Ter)
c.1060G>T (p.Glu354Ter)
c.985G>T (p.Glu329Ter)
c.928G>T (p.Glu310Ter)
3g.30672217A>CCA351808408TGFBR2c.1034A>C (p.Glu345Ala)
n.2630A>C
c.1109A>C (p.Glu370Ala)
c.1061A>C (p.Glu354Ala)
c.986A>C (p.Glu329Ala)
c.929A>C (p.Glu310Ala)
3g.30672217A>GCA351808409TGFBR2c.1034A>G (p.Glu345Gly)
n.2630A>G
c.1109A>G (p.Glu370Gly)
c.1061A>G (p.Glu354Gly)
c.986A>G (p.Glu329Gly)
c.929A>G (p.Glu310Gly)
 dbSNP
3g.30672217A>TCA351808407TGFBR2c.1034A>T (p.Glu345Val)
n.2630A>T
c.1109A>T (p.Glu370Val)
c.1061A>T (p.Glu354Val)
c.986A>T (p.Glu329Val)
c.929A>T (p.Glu310Val)
3g.30672218G>ACA433059019TGFBR2c.1035G>A (p.Glu345=)
n.2631G>A
c.1110G>A (p.Glu370=)
c.1062G>A (p.Glu354=)
c.987G>A (p.Glu329=)
c.930G>A (p.Glu310=)
 dbSNP
3g.30672218G>CCA351808410TGFBR2c.1035G>C (p.Glu345Asp)
n.2631G>C
c.1110G>C (p.Glu370Asp)
c.1062G>C (p.Glu354Asp)
c.987G>C (p.Glu329Asp)
c.930G>C (p.Glu310Asp)
3g.30672218G>TCA351808411TGFBR2c.1035G>T (p.Glu345Asp)
n.2631G>T
c.1110G>T (p.Glu370Asp)
c.1062G>T (p.Glu354Asp)
c.987G>T (p.Glu329Asp)
c.930G>T (p.Glu310Asp)
3g.30672219G>ACA351808412TGFBR2c.1036G>A (p.Asp346Asn)
n.2632G>A
c.1111G>A (p.Asp371Asn)
c.1063G>A (p.Asp355Asn)
c.988G>A (p.Asp330Asn)
c.931G>A (p.Asp311Asn)
 dbSNP
3g.30672219G>CCA351808413TGFBR2c.1036G>C (p.Asp346His)
n.2632G>C
c.1111G>C (p.Asp371His)
c.1063G>C (p.Asp355His)
c.988G>C (p.Asp330His)
c.931G>C (p.Asp311His)
3g.30672219G=CA1354873188TGFBR2c.1036G= (p.Asp346=)
n.2632G=
c.1111G= (p.Asp371=)
c.1063G= (p.Asp355=)
c.988G= (p.Asp330=)
c.931G= (p.Asp311=)
3g.30672219G>TCA351808414TGFBR2c.1036G>T (p.Asp346Tyr)
n.2632G>T
c.1111G>T (p.Asp371Tyr)
c.1063G>T (p.Asp355Tyr)
c.988G>T (p.Asp330Tyr)
c.931G>T (p.Asp311Tyr)
3g.30672219_30672220insCTCA1046447392TGFBR2c.1036_1037insCT (p.Asp346AlafsTer?)
n.2632_2633insCT
c.1111_1112insCT (p.Asp371AlafsTer?)
c.1063_1064insCT (p.Asp355AlafsTer?)
c.988_989insCT (p.Asp330AlafsTer?)
c.931_932insCT (p.Asp311AlafsTer?)
 dbSNP gnomAD v3 gnomAD v4
3g.30672220A>CCA351808415TGFBR2c.1037A>C (p.Asp346Ala)
n.2633A>C
c.1112A>C (p.Asp371Ala)
c.1064A>C (p.Asp355Ala)
c.989A>C (p.Asp330Ala)
c.932A>C (p.Asp311Ala)
3g.30672220A>GCA351808416TGFBR2c.1037A>G (p.Asp346Gly)
n.2633A>G
c.1112A>G (p.Asp371Gly)
c.1064A>G (p.Asp355Gly)
c.989A>G (p.Asp330Gly)
c.932A>G (p.Asp311Gly)
 dbSNP
3g.30672220A>TCA351808417TGFBR2c.1037A>T (p.Asp346Val)
n.2633A>T
c.1112A>T (p.Asp371Val)
c.1064A>T (p.Asp355Val)
c.989A>T (p.Asp330Val)
c.932A>T (p.Asp311Val)
 dbSNP
3g.30672220_30672221delinsACCA1354873189TGFBR2c.1037_1038delinsAC (p.Asp346=)
n.2633_2634delinsAC
c.1112_1113delinsAC (p.Asp371=)
c.1064_1065delinsAC (p.Asp355=)
c.989_990delinsAC (p.Asp330=)
c.932_933delinsAC (p.Asp311=)
3g.30672221C>ACA351808418TGFBR2c.1038C>A (p.Asp346Glu)
n.2634C>A
c.1113C>A (p.Asp371Glu)
c.1065C>A (p.Asp355Glu)
c.990C>A (p.Asp330Glu)
c.933C>A (p.Asp311Glu)
 dbSNP
3g.30672221C>GCA351808419TGFBR2c.1038C>G (p.Asp346Glu)
n.2634C>G
c.1113C>G (p.Asp371Glu)
c.1065C>G (p.Asp355Glu)
c.990C>G (p.Asp330Glu)
c.933C>G (p.Asp311Glu)
 dbSNP
3g.30672221C>TCA433059024TGFBR2c.1038C>T (p.Asp346=)
n.2634C>T
c.1113C>T (p.Asp371=)
c.1065C>T (p.Asp355=)
c.990C>T (p.Asp330=)
c.933C>T (p.Asp311=)
 dbSNP
3g.30672222delCA913188059TGFBR2c.1039del (p.Leu347CysfsTer?)
n.2635del
c.1114del (p.Leu372CysfsTer?)
c.1066del (p.Leu356CysfsTer?)
c.991del (p.Leu331CysfsTer?)
c.934del (p.Leu312CysfsTer?)
 ClinVar dbSNP
3g.30672222C>ACA351808420TGFBR2c.1039C>A (p.Leu347Met)
n.2635C>A
c.1114C>A (p.Leu372Met)
c.1066C>A (p.Leu356Met)
c.991C>A (p.Leu331Met)
c.934C>A (p.Leu312Met)
3g.30672222C=CA1354873190TGFBR2c.1039C= (p.Leu347=)
n.2635C=
c.1114C= (p.Leu372=)
c.1066C= (p.Leu356=)
c.991C= (p.Leu331=)
c.934C= (p.Leu312=)
3g.30672222C>GCA351808421TGFBR2c.1039C>G (p.Leu347Val)
n.2635C>G
c.1114C>G (p.Leu372Val)
c.1066C>G (p.Leu356Val)
c.991C>G (p.Leu331Val)
c.934C>G (p.Leu312Val)
3g.30672222C>TCA433059025TGFBR2c.1039C>T (p.Leu347=)
n.2635C>T
c.1114C>T (p.Leu372=)
c.1066C>T (p.Leu356=)
c.991C>T (p.Leu331=)
c.934C>T (p.Leu312=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672223T>ACA351808423TGFBR2c.1040T>A (p.Leu347Gln)
n.2636T>A
c.1115T>A (p.Leu372Gln)
c.1067T>A (p.Leu356Gln)
c.992T>A (p.Leu331Gln)
c.935T>A (p.Leu312Gln)
 ClinVar
3g.30672223T>CCA351808424TGFBR2c.1040T>C (p.Leu347Pro)
n.2636T>C
c.1115T>C (p.Leu372Pro)
c.1067T>C (p.Leu356Pro)
c.992T>C (p.Leu331Pro)
c.935T>C (p.Leu312Pro)
3g.30672223T>GCA351808422TGFBR2c.1040T>G (p.Leu347Arg)
n.2636T>G
c.1115T>G (p.Leu372Arg)
c.1067T>G (p.Leu356Arg)
c.992T>G (p.Leu331Arg)
c.935T>G (p.Leu312Arg)
3g.30672224G>ACA433059027TGFBR2c.1041G>A (p.Leu347=)
n.2637G>A
c.1116G>A (p.Leu372=)
c.1068G>A (p.Leu356=)
c.993G>A (p.Leu331=)
c.936G>A (p.Leu312=)
3g.30672224G>CCA433059029TGFBR2c.1041G>C (p.Leu347=)
n.2637G>C
c.1116G>C (p.Leu372=)
c.1068G>C (p.Leu356=)
c.993G>C (p.Leu331=)
c.936G>C (p.Leu312=)
 gnomAD v4
3g.30672224G>TCA433059031TGFBR2c.1041G>T (p.Leu347=)
n.2637G>T
c.1116G>T (p.Leu372=)
c.1068G>T (p.Leu356=)
c.993G>T (p.Leu331=)
c.936G>T (p.Leu312=)
3g.30672225C>ACA351808425TGFBR2c.1042C>A (p.Arg348Ser)
n.2638C>A
c.1117C>A (p.Arg373Ser)
c.1069C>A (p.Arg357Ser)
c.994C>A (p.Arg332Ser)
c.937C>A (p.Arg313Ser)
3g.30672225C=CA1354873191TGFBR2c.1042C= (p.Arg348=)
n.2638C=
c.1117C= (p.Arg373=)
c.1069C= (p.Arg357=)
c.994C= (p.Arg332=)
c.937C= (p.Arg313=)
3g.30672225C>GCA351808426TGFBR2c.1042C>G (p.Arg348Gly)
n.2638C>G
c.1117C>G (p.Arg373Gly)
c.1069C>G (p.Arg357Gly)
c.994C>G (p.Arg332Gly)
c.937C>G (p.Arg313Gly)
 dbSNP
3g.30672225C>TCA045456TGFBR2c.1042C>T (p.Arg348Cys)
n.2638C>T
c.1117C>T (p.Arg373Cys)
c.1069C>T (p.Arg357Cys)
c.994C>T (p.Arg332Cys)
c.937C>T (p.Arg313Cys)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672226G>ACA045468TGFBR2c.1043G>A (p.Arg348His)
n.2639G>A
c.1118G>A (p.Arg373His)
c.1070G>A (p.Arg357His)
c.995G>A (p.Arg332His)
c.938G>A (p.Arg313His)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.30672226G>CCA351808427TGFBR2c.1043G>C (p.Arg348Pro)
n.2639G>C
c.1118G>C (p.Arg373Pro)
c.1070G>C (p.Arg357Pro)
c.995G>C (p.Arg332Pro)
c.938G>C (p.Arg313Pro)
 dbSNP
3g.30672226G=CA1354873192TGFBR2c.1043G= (p.Arg348=)
n.2639G=
c.1118G= (p.Arg373=)
c.1070G= (p.Arg357=)
c.995G= (p.Arg332=)
c.938G= (p.Arg313=)
3g.30672226G>TCA351808428TGFBR2c.1043G>T (p.Arg348Leu)
n.2639G>T
c.1118G>T (p.Arg373Leu)
c.1070G>T (p.Arg357Leu)
c.995G>T (p.Arg332Leu)
c.938G>T (p.Arg313Leu)
 gnomAD v4
3g.30672227C>ACA433059033TGFBR2c.1044C>A (p.Arg348=)
n.2640C>A
c.1119C>A (p.Arg373=)
c.1071C>A (p.Arg357=)
c.996C>A (p.Arg332=)
c.939C>A (p.Arg313=)
 dbSNP
3g.30672227C>GCA433059034TGFBR2c.1044C>G (p.Arg348=)
n.2640C>G
c.1119C>G (p.Arg373=)
c.1071C>G (p.Arg357=)
c.996C>G (p.Arg332=)
c.939C>G (p.Arg313=)
 dbSNP
3g.30672227C>TCA433059036TGFBR2c.1044C>T (p.Arg348=)
n.2640C>T
c.1119C>T (p.Arg373=)
c.1071C>T (p.Arg357=)
c.996C>T (p.Arg332=)
c.939C>T (p.Arg313=)
 ClinVar gnomAD v4
3g.30672228A>CCA351808429TGFBR2c.1045A>C (p.Lys349Gln)
n.2641A>C
c.1120A>C (p.Lys374Gln)
c.1072A>C (p.Lys358Gln)
c.997A>C (p.Lys333Gln)
c.940A>C (p.Lys314Gln)
3g.30672228A>GCA351808431TGFBR2c.1045A>G (p.Lys349Glu)
n.2641A>G
c.1120A>G (p.Lys374Glu)
c.1072A>G (p.Lys358Glu)
c.997A>G (p.Lys333Glu)
c.940A>G (p.Lys314Glu)
 gnomAD v4
3g.30672228A>TCA351808430TGFBR2c.1045A>T (p.Lys349Ter)
n.2641A>T
c.1120A>T (p.Lys374Ter)
c.1072A>T (p.Lys358Ter)
c.997A>T (p.Lys333Ter)
c.940A>T (p.Lys314Ter)
3g.30672229A>CCA351808432TGFBR2c.1046A>C (p.Lys349Thr)
n.2642A>C
c.1121A>C (p.Lys374Thr)
c.1073A>C (p.Lys358Thr)
c.998A>C (p.Lys333Thr)
c.941A>C (p.Lys314Thr)
3g.30672229A>GCA351808433TGFBR2c.1046A>G (p.Lys349Arg)
n.2642A>G
c.1121A>G (p.Lys374Arg)
c.1073A>G (p.Lys358Arg)
c.998A>G (p.Lys333Arg)
c.941A>G (p.Lys314Arg)
3g.30672229A>TCA351808434TGFBR2c.1046A>T (p.Lys349Met)
n.2642A>T
c.1121A>T (p.Lys374Met)
c.1073A>T (p.Lys358Met)
c.998A>T (p.Lys333Met)
c.941A>T (p.Lys314Met)
3g.30672230G>ACA433059037TGFBR2c.1047G>A (p.Lys349=)
n.2643G>A
c.1122G>A (p.Lys374=)
c.1074G>A (p.Lys358=)
c.999G>A (p.Lys333=)
c.942G>A (p.Lys314=)
 ClinVar dbSNP
3g.30672230G>CCA351808435TGFBR2c.1047G>C (p.Lys349Asn)
n.2643G>C
c.1122G>C (p.Lys374Asn)
c.1074G>C (p.Lys358Asn)
c.999G>C (p.Lys333Asn)
c.942G>C (p.Lys314Asn)
 ClinVar dbSNP gnomAD v4
3g.30672230G>TCA351808436TGFBR2c.1047G>T (p.Lys349Asn)
n.2643G>T
c.1122G>T (p.Lys374Asn)
c.1074G>T (p.Lys358Asn)
c.999G>T (p.Lys333Asn)
c.942G>T (p.Lys314Asn)
3g.30672231C>ACA351808437TGFBR2c.1048C>A (p.Leu350Met)
n.2644C>A
c.1123C>A (p.Leu375Met)
c.1075C>A (p.Leu359Met)
c.1000C>A (p.Leu334Met)
c.943C>A (p.Leu315Met)
 dbSNP gnomAD v4
3g.30672231C=CA1354873193TGFBR2c.1048C= (p.Leu350=)
n.2644C=
c.1123C= (p.Leu375=)
c.1075C= (p.Leu359=)
c.1000C= (p.Leu334=)
c.943C= (p.Leu315=)
3g.30672231C>GCA351808438TGFBR2c.1048C>G (p.Leu350Val)
n.2644C>G
c.1123C>G (p.Leu375Val)
c.1075C>G (p.Leu359Val)
c.1000C>G (p.Leu334Val)
c.943C>G (p.Leu315Val)
3g.30672231C>TCA045484TGFBR2c.1048C>T (p.Leu350=)
n.2644C>T
c.1123C>T (p.Leu375=)
c.1075C>T (p.Leu359=)
c.1000C>T (p.Leu334=)
c.943C>T (p.Leu315=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672232T>ACA351808441TGFBR2c.1049T>A (p.Leu350Gln)
n.2645T>A
c.1124T>A (p.Leu375Gln)
c.1076T>A (p.Leu359Gln)
c.1001T>A (p.Leu334Gln)
c.944T>A (p.Leu315Gln)
 ClinVar gnomAD v4
3g.30672232T>CCA351808439TGFBR2c.1049T>C (p.Leu350Pro)
n.2645T>C
c.1124T>C (p.Leu375Pro)
c.1076T>C (p.Leu359Pro)
c.1001T>C (p.Leu334Pro)
c.944T>C (p.Leu315Pro)
 COSMIC COSMIC
3g.30672232T>GCA351808440TGFBR2c.1049T>G (p.Leu350Arg)
n.2645T>G
c.1124T>G (p.Leu375Arg)
c.1076T>G (p.Leu359Arg)
c.1001T>G (p.Leu334Arg)
c.944T>G (p.Leu315Arg)
3g.30672233G>ACA433059041TGFBR2c.1050G>A (p.Leu350=)
n.2646G>A
c.1125G>A (p.Leu375=)
c.1077G>A (p.Leu359=)
c.1002G>A (p.Leu334=)
c.945G>A (p.Leu315=)
 dbSNP
3g.30672233G>CCA433059043TGFBR2c.1050G>C (p.Leu350=)
n.2646G>C
c.1125G>C (p.Leu375=)
c.1077G>C (p.Leu359=)
c.1002G>C (p.Leu334=)
c.945G>C (p.Leu315=)
3g.30672233G>TCA433059045TGFBR2c.1050G>T (p.Leu350=)
n.2646G>T
c.1125G>T (p.Leu375=)
c.1077G>T (p.Leu359=)
c.1002G>T (p.Leu334=)
c.945G>T (p.Leu315=)
3g.30672234G>ACA351808442TGFBR2c.1051G>A (p.Gly351Ser)
n.2647G>A
c.1126G>A (p.Gly376Ser)
c.1078G>A (p.Gly360Ser)
c.1003G>A (p.Gly335Ser)
c.946G>A (p.Gly316Ser)
 dbSNP gnomAD v4
3g.30672234G>CCA351808443TGFBR2c.1051G>C (p.Gly351Arg)
n.2647G>C
c.1126G>C (p.Gly376Arg)
c.1078G>C (p.Gly360Arg)
c.1003G>C (p.Gly335Arg)
c.946G>C (p.Gly316Arg)
 ClinVar dbSNP
3g.30672234G=CA1354873194TGFBR2c.1051G= (p.Gly351=)
n.2647G=
c.1126G= (p.Gly376=)
c.1078G= (p.Gly360=)
c.1003G= (p.Gly335=)
c.946G= (p.Gly316=)
3g.30672234G>TCA351808444TGFBR2c.1051G>T (p.Gly351Cys)
n.2647G>T
c.1126G>T (p.Gly376Cys)
c.1078G>T (p.Gly360Cys)
c.1003G>T (p.Gly335Cys)
c.946G>T (p.Gly316Cys)
 dbSNP
3g.30672235G>ACA351866TGFBR2c.1052G>A (p.Gly351Asp)
n.2648G>A
c.1127G>A (p.Gly376Asp)
c.1079G>A (p.Gly360Asp)
c.1004G>A (p.Gly335Asp)
c.947G>A (p.Gly316Asp)
 ClinVar dbSNP
3g.30672235G>CCA351808445TGFBR2c.1052G>C (p.Gly351Ala)
n.2648G>C
c.1127G>C (p.Gly376Ala)
c.1079G>C (p.Gly360Ala)
c.1004G>C (p.Gly335Ala)
c.947G>C (p.Gly316Ala)
 dbSNP
3g.30672235G=CA1354873195TGFBR2c.1052G= (p.Gly351=)
n.2648G=
c.1127G= (p.Gly376=)
c.1079G= (p.Gly360=)
c.1004G= (p.Gly335=)
c.947G= (p.Gly316=)
3g.30672235G>TCA351808446TGFBR2c.1052G>T (p.Gly351Val)
n.2648G>T
c.1127G>T (p.Gly376Val)
c.1079G>T (p.Gly360Val)
c.1004G>T (p.Gly335Val)
c.947G>T (p.Gly316Val)
 dbSNP
3g.30672236C>ACA433059047TGFBR2c.1053C>A (p.Gly351=)
n.2649C>A
c.1128C>A (p.Gly376=)
c.1080C>A (p.Gly360=)
c.1005C>A (p.Gly335=)
c.948C>A (p.Gly316=)
 ClinVar dbSNP gnomAD v4
3g.30672236C=CA1354873196TGFBR2c.1053C= (p.Gly351=)
n.2649C=
c.1128C= (p.Gly376=)
c.1080C= (p.Gly360=)
c.1005C= (p.Gly335=)
c.948C= (p.Gly316=)
3g.30672236C>GCA433059048TGFBR2c.1053C>G (p.Gly351=)
n.2649C>G
c.1128C>G (p.Gly376=)
c.1080C>G (p.Gly360=)
c.1005C>G (p.Gly335=)
c.948C>G (p.Gly316=)
3g.30672236C>TCA433059049TGFBR2c.1053C>T (p.Gly351=)
n.2649C>T
c.1128C>T (p.Gly376=)
c.1080C>T (p.Gly360=)
c.1005C>T (p.Gly335=)
c.948C>T (p.Gly316=)
 dbSNP gnomAD v2
3g.30672237A>CCA351808447TGFBR2c.1054A>C (p.Ser352Arg)
n.2650A>C
c.1129A>C (p.Ser377Arg)
c.1081A>C (p.Ser361Arg)
c.1006A>C (p.Ser336Arg)
c.949A>C (p.Ser317Arg)
3g.30672237A>GCA351808448TGFBR2c.1054A>G (p.Ser352Gly)
n.2650A>G
c.1129A>G (p.Ser377Gly)
c.1081A>G (p.Ser361Gly)
c.1006A>G (p.Ser336Gly)
c.949A>G (p.Ser317Gly)
 dbSNP
3g.30672237A>TCA351808449TGFBR2c.1054A>T (p.Ser352Cys)
n.2650A>T
c.1129A>T (p.Ser377Cys)
c.1081A>T (p.Ser361Cys)
c.1006A>T (p.Ser336Cys)
c.949A>T (p.Ser317Cys)
 dbSNP
3g.30672238G>ACA351808450TGFBR2c.1055G>A (p.Ser352Asn)
n.2651G>A
c.1130G>A (p.Ser377Asn)
c.1082G>A (p.Ser361Asn)
c.1007G>A (p.Ser336Asn)
c.950G>A (p.Ser317Asn)
 dbSNP gnomAD v4
3g.30672238G>CCA351808451TGFBR2c.1055G>C (p.Ser352Thr)
n.2651G>C
c.1130G>C (p.Ser377Thr)
c.1082G>C (p.Ser361Thr)
c.1007G>C (p.Ser336Thr)
c.950G>C (p.Ser317Thr)
 dbSNP
3g.30672238G>TCA351808452TGFBR2c.1055G>T (p.Ser352Ile)
n.2651G>T
c.1130G>T (p.Ser377Ile)
c.1082G>T (p.Ser361Ile)
c.1007G>T (p.Ser336Ile)
c.950G>T (p.Ser317Ile)
3g.30672239C>ACA351808453TGFBR2c.1056C>A (p.Ser352Arg)
n.2652C>A
c.1131C>A (p.Ser377Arg)
c.1083C>A (p.Ser361Arg)
c.1008C>A (p.Ser336Arg)
c.951C>A (p.Ser317Arg)
 dbSNP
3g.30672239C=CA1354873197TGFBR2c.1056C= (p.Ser352=)
n.2652C=
c.1131C= (p.Ser377=)
c.1083C= (p.Ser361=)
c.1008C= (p.Ser336=)
c.951C= (p.Ser317=)
3g.30672239C>GCA71528616TGFBR2c.1056C>G (p.Ser352Arg)
n.2652C>G
c.1131C>G (p.Ser377Arg)
c.1083C>G (p.Ser361Arg)
c.1008C>G (p.Ser336Arg)
c.951C>G (p.Ser317Arg)
 ClinVar dbSNP gnomAD v4
3g.30672239C>TCA433059050TGFBR2c.1056C>T (p.Ser352=)
n.2652C>T
c.1131C>T (p.Ser377=)
c.1083C>T (p.Ser361=)
c.1008C>T (p.Ser336=)
c.951C>T (p.Ser317=)
 dbSNP
3g.30672240T>ACA351808454TGFBR2c.1057T>A (p.Ser353Thr)
n.2653T>A
c.1132T>A (p.Ser378Thr)
c.1084T>A (p.Ser362Thr)
c.1009T>A (p.Ser337Thr)
c.952T>A (p.Ser318Thr)
 dbSNP
3g.30672240T>CCA351808455TGFBR2c.1057T>C (p.Ser353Pro)
n.2653T>C
c.1132T>C (p.Ser378Pro)
c.1084T>C (p.Ser362Pro)
c.1009T>C (p.Ser337Pro)
c.952T>C (p.Ser318Pro)
 dbSNP
3g.30672240T>GCA351808456TGFBR2c.1057T>G (p.Ser353Ala)
n.2653T>G
c.1132T>G (p.Ser378Ala)
c.1084T>G (p.Ser362Ala)
c.1009T>G (p.Ser337Ala)
c.952T>G (p.Ser318Ala)
3g.30672241C>ACA351808457TGFBR2c.1058C>A (p.Ser353Tyr)
n.2654C>A
c.1133C>A (p.Ser378Tyr)
c.1085C>A (p.Ser362Tyr)
c.1010C>A (p.Ser337Tyr)
c.953C>A (p.Ser318Tyr)
3g.30672241C=CA1354873198TGFBR2c.1058C= (p.Ser353=)
n.2654C=
c.1133C= (p.Ser378=)
c.1085C= (p.Ser362=)
c.1010C= (p.Ser337=)
c.953C= (p.Ser318=)
3g.30672241C>GCA351808458TGFBR2c.1058C>G (p.Ser353Cys)
n.2654C>G
c.1133C>G (p.Ser378Cys)
c.1085C>G (p.Ser362Cys)
c.1010C>G (p.Ser337Cys)
c.953C>G (p.Ser318Cys)
 dbSNP
3g.30672241C>TCA351808459TGFBR2c.1058C>T (p.Ser353Phe)
n.2654C>T
c.1133C>T (p.Ser378Phe)
c.1085C>T (p.Ser362Phe)
c.1010C>T (p.Ser337Phe)
c.953C>T (p.Ser318Phe)
 ClinVar dbSNP COSMIC
3g.30672242C>ACA433059057TGFBR2c.1059C>A (p.Ser353=)
n.2655C>A
c.1134C>A (p.Ser378=)
c.1086C>A (p.Ser362=)
c.1011C>A (p.Ser337=)
c.954C>A (p.Ser318=)
 ClinVar dbSNP
3g.30672242C>GCA433059059TGFBR2c.1059C>G (p.Ser353=)
n.2655C>G
c.1134C>G (p.Ser378=)
c.1086C>G (p.Ser362=)
c.1011C>G (p.Ser337=)
c.954C>G (p.Ser318=)
 dbSNP
3g.30672242C>TCA433059061TGFBR2c.1059C>T (p.Ser353=)
n.2655C>T
c.1134C>T (p.Ser378=)
c.1086C>T (p.Ser362=)
c.1011C>T (p.Ser337=)
c.954C>T (p.Ser318=)
 ClinVar dbSNP
3g.30672243C>ACA045505TGFBR2c.1060C>A (p.Leu354Ile)
n.2656C>A
c.1135C>A (p.Leu379Ile)
c.1087C>A (p.Leu363Ile)
c.1012C>A (p.Leu338Ile)
c.955C>A (p.Leu319Ile)
 dbSNP ExAC
3g.30672243C=CA1354873199TGFBR2c.1060C= (p.Leu354=)
n.2656C=
c.1135C= (p.Leu379=)
c.1087C= (p.Leu363=)
c.1012C= (p.Leu338=)
c.955C= (p.Leu319=)
3g.30672243C>GCA351808460TGFBR2c.1060C>G (p.Leu354Val)
n.2656C>G
c.1135C>G (p.Leu379Val)
c.1087C>G (p.Leu363Val)
c.1012C>G (p.Leu338Val)
c.955C>G (p.Leu319Val)
 dbSNP
3g.30672243C>TCA351808461TGFBR2c.1060C>T (p.Leu354Phe)
n.2656C>T
c.1135C>T (p.Leu379Phe)
c.1087C>T (p.Leu363Phe)
c.1012C>T (p.Leu338Phe)
c.955C>T (p.Leu319Phe)
 dbSNP
3g.30672244T>ACA351808462TGFBR2c.1061T>A (p.Leu354His)
n.2657T>A
c.1136T>A (p.Leu379His)
c.1088T>A (p.Leu363His)
c.1013T>A (p.Leu338His)
c.956T>A (p.Leu319His)
 dbSNP
3g.30672244T>CCA351808463TGFBR2c.1061T>C (p.Leu354Pro)
n.2657T>C
c.1136T>C (p.Leu379Pro)
c.1088T>C (p.Leu363Pro)
c.1013T>C (p.Leu338Pro)
c.956T>C (p.Leu319Pro)
3g.30672244T>GCA351808464TGFBR2c.1061T>G (p.Leu354Arg)
n.2657T>G
c.1136T>G (p.Leu379Arg)
c.1088T>G (p.Leu363Arg)
c.1013T>G (p.Leu338Arg)
c.956T>G (p.Leu319Arg)
 COSMIC COSMIC
3g.30672245C>ACA433059070TGFBR2c.1062C>A (p.Leu354=)
n.2658C>A
c.1137C>A (p.Leu379=)
c.1089C>A (p.Leu363=)
c.1014C>A (p.Leu338=)
c.957C>A (p.Leu319=)
3g.30672245C=CA1354873200TGFBR2c.1062C= (p.Leu354=)
n.2658C=
c.1137C= (p.Leu379=)
c.1089C= (p.Leu363=)
c.1014C= (p.Leu338=)
c.957C= (p.Leu319=)
3g.30672245C>GCA433059069TGFBR2c.1062C>G (p.Leu354=)
n.2658C>G
c.1137C>G (p.Leu379=)
c.1089C>G (p.Leu363=)
c.1014C>G (p.Leu338=)
c.957C>G (p.Leu319=)
 dbSNP
3g.30672245C>TCA020586TGFBR2c.1062C>T (p.Leu354=)
n.2658C>T
c.1137C>T (p.Leu379=)
c.1089C>T (p.Leu363=)
c.1014C>T (p.Leu338=)
c.957C>T (p.Leu319=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672246G>ACA16604494TGFBR2c.1063G>A (p.Ala355Thr)
n.2659G>A
c.1138G>A (p.Ala380Thr)
c.1090G>A (p.Ala364Thr)
c.1015G>A (p.Ala339Thr)
c.958G>A (p.Ala320Thr)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672246G>CCA020590TGFBR2c.1063G>C (p.Ala355Pro)
n.2659G>C
c.1138G>C (p.Ala380Pro)
c.1090G>C (p.Ala364Pro)
c.1015G>C (p.Ala339Pro)
c.958G>C (p.Ala320Pro)
 ClinVar dbSNP
3g.30672246G=CA1354873201TGFBR2c.1063G= (p.Ala355=)
n.2659G=
c.1138G= (p.Ala380=)
c.1090G= (p.Ala364=)
c.1015G= (p.Ala339=)
c.958G= (p.Ala320=)
3g.30672246G>TCA045538TGFBR2c.1063G>T (p.Ala355Ser)
n.2659G>T
c.1138G>T (p.Ala380Ser)
c.1090G>T (p.Ala364Ser)
c.1015G>T (p.Ala339Ser)
c.958G>T (p.Ala320Ser)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672247C>ACA351808465TGFBR2c.1064C>A (p.Ala355Asp)
n.2660C>A
c.1139C>A (p.Ala380Asp)
c.1091C>A (p.Ala364Asp)
c.1016C>A (p.Ala339Asp)
c.959C>A (p.Ala320Asp)
 dbSNP
3g.30672247C=CA1354873202TGFBR2c.1064C= (p.Ala355=)
n.2660C=
c.1139C= (p.Ala380=)
c.1091C= (p.Ala364=)
c.1016C= (p.Ala339=)
c.959C= (p.Ala320=)
3g.30672247C>GCA351808466TGFBR2c.1064C>G (p.Ala355Gly)
n.2660C>G
c.1139C>G (p.Ala380Gly)
c.1091C>G (p.Ala364Gly)
c.1016C>G (p.Ala339Gly)
c.959C>G (p.Ala320Gly)
 dbSNP
3g.30672247C>TCA045550TGFBR2c.1064C>T (p.Ala355Val)
n.2660C>T
c.1139C>T (p.Ala380Val)
c.1091C>T (p.Ala364Val)
c.1016C>T (p.Ala339Val)
c.959C>T (p.Ala320Val)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672249dupCA645535107TGFBR2c.1066dup (p.Arg356ProfsTer9)
n.2662dup
c.1141dup (p.Arg381ProfsTer9)
c.1093dup (p.Arg365ProfsTer9)
c.1018dup (p.Arg340ProfsTer9)
c.961dup (p.Arg321ProfsTer9)
 gnomAD v4 COSMIC
3g.30672248C>ACA433059074TGFBR2c.1065C>A (p.Ala355=)
n.2661C>A
c.1140C>A (p.Ala380=)
c.1092C>A (p.Ala364=)
c.1017C>A (p.Ala339=)
c.960C>A (p.Ala320=)
 dbSNP
3g.30672248C>GCA433059076TGFBR2c.1065C>G (p.Ala355=)
n.2661C>G
c.1140C>G (p.Ala380=)
c.1092C>G (p.Ala364=)
c.1017C>G (p.Ala339=)
c.960C>G (p.Ala320=)
 dbSNP
3g.30672248C>TCA433059077TGFBR2c.1065C>T (p.Ala355=)
n.2661C>T
c.1140C>T (p.Ala380=)
c.1092C>T (p.Ala364=)
c.1017C>T (p.Ala339=)
c.960C>T (p.Ala320=)
 dbSNP
3g.30672249C>ACA433059078TGFBR2c.1066C>A (p.Arg356=)
n.2662C>A
c.1141C>A (p.Arg381=)
c.1093C>A (p.Arg365=)
c.1018C>A (p.Arg340=)
c.961C>A (p.Arg321=)
3g.30672249C=CA1354873203TGFBR2c.1066C= (p.Arg356=)
n.2662C=
c.1141C= (p.Arg381=)
c.1093C= (p.Arg365=)
c.1018C= (p.Arg340=)
c.961C= (p.Arg321=)
3g.30672249C>GCA322326TGFBR2c.1066C>G (p.Arg356Gly)
n.2662C>G
c.1141C>G (p.Arg381Gly)
c.1093C>G (p.Arg365Gly)
c.1018C>G (p.Arg340Gly)
c.961C>G (p.Arg321Gly)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672249C>TCA045560TGFBR2c.1066C>T (p.Arg356Trp)
n.2662C>T
c.1141C>T (p.Arg381Trp)
c.1093C>T (p.Arg365Trp)
c.1018C>T (p.Arg340Trp)
c.961C>T (p.Arg321Trp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.30672250G>ACA045577TGFBR2c.1067G>A (p.Arg356Gln)
n.2663G>A
c.1142G>A (p.Arg381Gln)
c.1094G>A (p.Arg365Gln)
c.1019G>A (p.Arg340Gln)
c.962G>A (p.Arg321Gln)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC
3g.30672250G>CCA020594TGFBR2c.1067G>C (p.Arg356Pro)
n.2663G>C
c.1142G>C (p.Arg381Pro)
c.1094G>C (p.Arg365Pro)
c.1019G>C (p.Arg340Pro)
c.962G>C (p.Arg321Pro)
 ClinVar dbSNP gnomAD v4
3g.30672250G=CA1354873204TGFBR2c.1067G= (p.Arg356=)
n.2663G=
c.1142G= (p.Arg381=)
c.1094G= (p.Arg365=)
c.1019G= (p.Arg340=)
c.962G= (p.Arg321=)
3g.30672250G>TCA351808467TGFBR2c.1067G>T (p.Arg356Leu)
n.2663G>T
c.1142G>T (p.Arg381Leu)
c.1094G>T (p.Arg365Leu)
c.1019G>T (p.Arg340Leu)
c.962G>T (p.Arg321Leu)
3g.30672250_30672251insCCA433059083TGFBR2c.1067_1068insC (p.Ile358AspfsTer7)
n.2663_2664insC
c.1142_1143insC (p.Ile383AspfsTer7)
c.1094_1095insC (p.Ile367AspfsTer7)
c.1019_1020insC (p.Ile342AspfsTer7)
c.962_963insC (p.Ile323AspfsTer7)
3g.30672251G>ACA433059084TGFBR2c.1068G>A (p.Arg356=)
n.2664G>A
c.1143G>A (p.Arg381=)
c.1095G>A (p.Arg365=)
c.1020G>A (p.Arg340=)
c.963G>A (p.Arg321=)
 dbSNP
3g.30672251G>CCA433059085TGFBR2c.1068G>C (p.Arg356=)
n.2664G>C
c.1143G>C (p.Arg381=)
c.1095G>C (p.Arg365=)
c.1020G>C (p.Arg340=)
c.963G>C (p.Arg321=)
 dbSNP gnomAD v2 gnomAD v4
3g.30672251G=CA1354873205TGFBR2c.1068G= (p.Arg356=)
n.2664G=
c.1143G= (p.Arg381=)
c.1095G= (p.Arg365=)
c.1020G= (p.Arg340=)
c.963G= (p.Arg321=)
3g.30672251G>TCA433059086TGFBR2c.1068G>T (p.Arg356=)
n.2664G>T
c.1143G>T (p.Arg381=)
c.1095G>T (p.Arg365=)
c.1020G>T (p.Arg340=)
c.963G>T (p.Arg321=)
 dbSNP
3g.30672252G>ACA351808468TGFBR2c.1069G>A (p.Gly357Arg)
n.2665G>A
c.1144G>A (p.Gly382Arg)
c.1096G>A (p.Gly366Arg)
c.1021G>A (p.Gly341Arg)
c.964G>A (p.Gly322Arg)
3g.30672252G>CCA351808469TGFBR2c.1069G>C (p.Gly357Arg)
n.2665G>C
c.1144G>C (p.Gly382Arg)
c.1096G>C (p.Gly366Arg)
c.1021G>C (p.Gly341Arg)
c.964G>C (p.Gly322Arg)
3g.30672252G=CA1354873206TGFBR2c.1069G= (p.Gly357=)
n.2665G=
c.1144G= (p.Gly382=)
c.1096G= (p.Gly366=)
c.1021G= (p.Gly341=)
c.964G= (p.Gly322=)
3g.30672252G>TCA020598TGFBR2c.1069G>T (p.Gly357Trp)
n.2665G>T
c.1144G>T (p.Gly382Trp)
c.1096G>T (p.Gly366Trp)
c.1021G>T (p.Gly341Trp)
c.964G>T (p.Gly322Trp)
 ClinVar dbSNP
3g.30672253G>ACA351808471TGFBR2c.1070G>A (p.Gly357Glu)
n.2666G>A
c.1145G>A (p.Gly382Glu)
c.1097G>A (p.Gly366Glu)
c.1022G>A (p.Gly341Glu)
c.965G>A (p.Gly322Glu)
 dbSNP
3g.30672253G>CCA045607TGFBR2c.1070G>C (p.Gly357Ala)
n.2666G>C
c.1145G>C (p.Gly382Ala)
c.1097G>C (p.Gly366Ala)
c.1022G>C (p.Gly341Ala)
c.965G>C (p.Gly322Ala)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672253G=CA1354873207TGFBR2c.1070G= (p.Gly357=)
n.2666G=
c.1145G= (p.Gly382=)
c.1097G= (p.Gly366=)
c.1022G= (p.Gly341=)
c.965G= (p.Gly322=)
3g.30672253G>TCA351808470TGFBR2c.1070G>T (p.Gly357Val)
n.2666G>T
c.1145G>T (p.Gly382Val)
c.1097G>T (p.Gly366Val)
c.1022G>T (p.Gly341Val)
c.965G>T (p.Gly322Val)
3g.30672254G>ACA433059090TGFBR2c.1071G>A (p.Gly357=)
n.2667G>A
c.1146G>A (p.Gly382=)
c.1098G>A (p.Gly366=)
c.1023G>A (p.Gly341=)
c.966G>A (p.Gly322=)
 ClinVar dbSNP gnomAD v4
3g.30672254G>CCA433059091TGFBR2c.1071G>C (p.Gly357=)
n.2667G>C
c.1146G>C (p.Gly382=)
c.1098G>C (p.Gly366=)
c.1023G>C (p.Gly341=)
c.966G>C (p.Gly322=)
 dbSNP gnomAD v4
3g.30672254G=CA1354873208TGFBR2c.1071G= (p.Gly357=)
n.2667G=
c.1146G= (p.Gly382=)
c.1098G= (p.Gly366=)
c.1023G= (p.Gly341=)
c.966G= (p.Gly322=)
3g.30672254G>TCA433059092TGFBR2c.1071G>T (p.Gly357=)
n.2667G>T
c.1146G>T (p.Gly382=)
c.1098G>T (p.Gly366=)
c.1023G>T (p.Gly341=)
c.966G>T (p.Gly322=)
 dbSNP gnomAD v3 gnomAD v4
3g.30672255A=CA1354873209TGFBR2c.1072A= (p.Ile358=)
n.2668A=
c.1147A= (p.Ile383=)
c.1099A= (p.Ile367=)
c.1024A= (p.Ile342=)
c.967A= (p.Ile323=)
3g.30672255A>CCA351808472TGFBR2c.1072A>C (p.Ile358Leu)
n.2668A>C
c.1147A>C (p.Ile383Leu)
c.1099A>C (p.Ile367Leu)
c.1024A>C (p.Ile342Leu)
c.967A>C (p.Ile323Leu)
 dbSNP
3g.30672255A>GCA351808473TGFBR2c.1072A>G (p.Ile358Val)
n.2668A>G
c.1147A>G (p.Ile383Val)
c.1099A>G (p.Ile367Val)
c.1024A>G (p.Ile342Val)
c.967A>G (p.Ile323Val)
 dbSNP gnomAD v3 gnomAD v4
3g.30672255A>TCA351808474TGFBR2c.1072A>T (p.Ile358Phe)
n.2668A>T
c.1147A>T (p.Ile383Phe)
c.1099A>T (p.Ile367Phe)
c.1024A>T (p.Ile342Phe)
c.967A>T (p.Ile323Phe)
 dbSNP gnomAD v4
3g.30672256T>ACA351808475TGFBR2c.1073T>A (p.Ile358Asn)
n.2669T>A
c.1148T>A (p.Ile383Asn)
c.1100T>A (p.Ile367Asn)
c.1025T>A (p.Ile342Asn)
c.968T>A (p.Ile323Asn)
3g.30672256T>CCA351808476TGFBR2c.1073T>C (p.Ile358Thr)
n.2669T>C
c.1148T>C (p.Ile383Thr)
c.1100T>C (p.Ile367Thr)
c.1025T>C (p.Ile342Thr)
c.968T>C (p.Ile323Thr)
 dbSNP gnomAD v4
3g.30672256T>GCA351808477TGFBR2c.1073T>G (p.Ile358Ser)
n.2669T>G
c.1148T>G (p.Ile383Ser)
c.1100T>G (p.Ile367Ser)
c.1025T>G (p.Ile342Ser)
c.968T>G (p.Ile323Ser)
 dbSNP
3g.30672256T=CA1354873210TGFBR2c.1073T= (p.Ile358=)
n.2669T=
c.1148T= (p.Ile383=)
c.1100T= (p.Ile367=)
c.1025T= (p.Ile342=)
c.968T= (p.Ile323=)
3g.30672257T>ACA433059095TGFBR2c.1074T>A (p.Ile358=)
n.2670T>A
c.1149T>A (p.Ile383=)
c.1101T>A (p.Ile367=)
c.1026T>A (p.Ile342=)
c.969T>A (p.Ile323=)
 dbSNP
3g.30672257T>CCA433059096TGFBR2c.1074T>C (p.Ile358=)
n.2670T>C
c.1149T>C (p.Ile383=)
c.1101T>C (p.Ile367=)
c.1026T>C (p.Ile342=)
c.969T>C (p.Ile323=)
3g.30672257T>GCA351808478TGFBR2c.1074T>G (p.Ile358Met)
n.2670T>G
c.1149T>G (p.Ile383Met)
c.1101T>G (p.Ile367Met)
c.1026T>G (p.Ile342Met)
c.969T>G (p.Ile323Met)
3g.30672258G>ACA351808479TGFBR2c.1075G>A (p.Ala359Thr)
n.2671G>A
c.1150G>A (p.Ala384Thr)
c.1102G>A (p.Ala368Thr)
c.1027G>A (p.Ala343Thr)
c.970G>A (p.Ala324Thr)
 dbSNP
3g.30672258G>CCA351808480TGFBR2c.1075G>C (p.Ala359Pro)
n.2671G>C
c.1150G>C (p.Ala384Pro)
c.1102G>C (p.Ala368Pro)
c.1027G>C (p.Ala343Pro)
c.970G>C (p.Ala324Pro)
 dbSNP
3g.30672258G>TCA351808481TGFBR2c.1075G>T (p.Ala359Ser)
n.2671G>T
c.1150G>T (p.Ala384Ser)
c.1102G>T (p.Ala368Ser)
c.1027G>T (p.Ala343Ser)
c.970G>T (p.Ala324Ser)
 gnomAD v4
3g.30672259C>ACA351808482TGFBR2c.1076C>A (p.Ala359Asp)
n.2672C>A
c.1151C>A (p.Ala384Asp)
c.1103C>A (p.Ala368Asp)
c.1028C>A (p.Ala343Asp)
c.971C>A (p.Ala324Asp)
 dbSNP
3g.30672259C>GCA351808483TGFBR2c.1076C>G (p.Ala359Gly)
n.2672C>G
c.1151C>G (p.Ala384Gly)
c.1103C>G (p.Ala368Gly)
c.1028C>G (p.Ala343Gly)
c.971C>G (p.Ala324Gly)
 dbSNP
3g.30672259C>TCA351808484TGFBR2c.1076C>T (p.Ala359Val)
n.2672C>T
c.1151C>T (p.Ala384Val)
c.1103C>T (p.Ala368Val)
c.1028C>T (p.Ala343Val)
c.971C>T (p.Ala324Val)
 dbSNP
3g.30672260T>ACA432917567TGFBR2c.1077T>A (p.Ala359=)
n.2673T>A
c.1152T>A (p.Ala384=)
c.1104T>A (p.Ala368=)
c.1029T>A (p.Ala343=)
c.972T>A (p.Ala324=)
 dbSNP
3g.30672260T>CCA432917568TGFBR2c.1077T>C (p.Ala359=)
n.2673T>C
c.1152T>C (p.Ala384=)
c.1104T>C (p.Ala368=)
c.1029T>C (p.Ala343=)
c.972T>C (p.Ala324=)
 ClinVar dbSNP
3g.30672260T>GCA432917566TGFBR2c.1077T>G (p.Ala359=)
n.2673T>G
c.1152T>G (p.Ala384=)
c.1104T>G (p.Ala368=)
c.1029T>G (p.Ala343=)
c.972T>G (p.Ala324=)
3g.30672260T=CA1354873211TGFBR2c.1077T= (p.Ala359=)
n.2673T=
c.1152T= (p.Ala384=)
c.1104T= (p.Ala368=)
c.1029T= (p.Ala343=)
c.972T= (p.Ala324=)
3g.30672261C>ACA351808486TGFBR2c.1078C>A (p.His360Asn)
n.2674C>A
c.1153C>A (p.His385Asn)
c.1105C>A (p.His369Asn)
c.1030C>A (p.His344Asn)
c.973C>A (p.His325Asn)
 dbSNP
3g.30672261C=CA1354873212TGFBR2c.1078C= (p.His360=)
n.2674C=
c.1153C= (p.His385=)
c.1105C= (p.His369=)
c.1030C= (p.His344=)
c.973C= (p.His325=)
3g.30672261C>GCA045619TGFBR2c.1078C>G (p.His360Asp)
n.2674C>G
c.1153C>G (p.His385Asp)
c.1105C>G (p.His369Asp)
c.1030C>G (p.His344Asp)
c.973C>G (p.His325Asp)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672261C>TCA351808485TGFBR2c.1078C>T (p.His360Tyr)
n.2674C>T
c.1153C>T (p.His385Tyr)
c.1105C>T (p.His369Tyr)
c.1030C>T (p.His344Tyr)
c.973C>T (p.His325Tyr)
 ClinVar dbSNP
3g.30672262A>CCA351808489TGFBR2c.1079A>C (p.His360Pro)
n.2675A>C
c.1154A>C (p.His385Pro)
c.1106A>C (p.His369Pro)
c.1031A>C (p.His344Pro)
c.974A>C (p.His325Pro)
 dbSNP
3g.30672262A>GCA351808487TGFBR2c.1079A>G (p.His360Arg)
n.2675A>G
c.1154A>G (p.His385Arg)
c.1106A>G (p.His369Arg)
c.1031A>G (p.His344Arg)
c.974A>G (p.His325Arg)
 dbSNP
3g.30672262A>TCA351808488TGFBR2c.1079A>T (p.His360Leu)
n.2675A>T
c.1154A>T (p.His385Leu)
c.1106A>T (p.His369Leu)
c.1031A>T (p.His344Leu)
c.974A>T (p.His325Leu)
 dbSNP
3g.30672262_30672265delinsACCTCA1354873213TGFBR2c.1079_1082delinsACCT (p.His360=)
n.2675_2678delinsACCT
c.1154_1157delinsACCT (p.His385=)
c.1106_1109delinsACCT (p.His369=)
c.1031_1034delinsACCT (p.His344=)
c.974_977delinsACCT (p.His325=)
3g.30672263C>ACA351808490TGFBR2c.1080C>A (p.His360Gln)
n.2676C>A
c.1155C>A (p.His385Gln)
c.1107C>A (p.His369Gln)
c.1032C>A (p.His344Gln)
c.975C>A (p.His325Gln)
 dbSNP gnomAD v4
3g.30672263C>GCA351808491TGFBR2c.1080C>G (p.His360Gln)
n.2676C>G
c.1155C>G (p.His385Gln)
c.1107C>G (p.His369Gln)
c.1032C>G (p.His344Gln)
c.975C>G (p.His325Gln)
 dbSNP
3g.30672263C>TCA432917569TGFBR2c.1080C>T (p.His360=)
n.2676C>T
c.1155C>T (p.His385=)
c.1107C>T (p.His369=)
c.1032C>T (p.His344=)
c.975C>T (p.His325=)
 ClinVar dbSNP gnomAD v4
3g.30672265_30672267delCA020601TGFBR2c.1082_1084del (p.Leu361del)
n.2678_2680del
c.1157_1159del (p.Leu386del)
c.1109_1111del (p.Leu370del)
c.1034_1036del (p.Leu345del)
c.977_979del (p.Leu326del)
 ClinVar dbSNP
3g.30672264C>ACA351808492TGFBR2c.1081C>A (p.Leu361Ile)
n.2677C>A
c.1156C>A (p.Leu386Ile)
c.1108C>A (p.Leu370Ile)
c.1033C>A (p.Leu345Ile)
c.976C>A (p.Leu326Ile)
 dbSNP
3g.30672264C>GCA351808493TGFBR2c.1081C>G (p.Leu361Val)
n.2677C>G
c.1156C>G (p.Leu386Val)
c.1108C>G (p.Leu370Val)
c.1033C>G (p.Leu345Val)
c.976C>G (p.Leu326Val)
 dbSNP
3g.30672264C>TCA351808494TGFBR2c.1081C>T (p.Leu361Phe)
n.2677C>T
c.1156C>T (p.Leu386Phe)
c.1108C>T (p.Leu370Phe)
c.1033C>T (p.Leu345Phe)
c.976C>T (p.Leu326Phe)
 dbSNP COSMIC COSMIC
3g.30672265T>ACA351808495TGFBR2c.1082T>A (p.Leu361His)
n.2678T>A
c.1157T>A (p.Leu386His)
c.1109T>A (p.Leu370His)
c.1034T>A (p.Leu345His)
c.977T>A (p.Leu326His)
 COSMIC COSMIC
3g.30672265T>CCA351808496TGFBR2c.1082T>C (p.Leu361Pro)
n.2678T>C
c.1157T>C (p.Leu386Pro)
c.1109T>C (p.Leu370Pro)
c.1034T>C (p.Leu345Pro)
c.977T>C (p.Leu326Pro)
 ClinVar
3g.30672265T>GCA351808497TGFBR2c.1082T>G (p.Leu361Arg)
n.2678T>G
c.1157T>G (p.Leu386Arg)
c.1109T>G (p.Leu370Arg)
c.1034T>G (p.Leu345Arg)
c.977T>G (p.Leu326Arg)
 COSMIC COSMIC
3g.30672266C>ACA432917572TGFBR2c.1083C>A (p.Leu361=)
n.2679C>A
c.1158C>A (p.Leu386=)
c.1110C>A (p.Leu370=)
c.1035C>A (p.Leu345=)
c.978C>A (p.Leu326=)
 dbSNP
3g.30672266C>GCA432917570TGFBR2c.1083C>G (p.Leu361=)
n.2679C>G
c.1158C>G (p.Leu386=)
c.1110C>G (p.Leu370=)
c.1035C>G (p.Leu345=)
c.978C>G (p.Leu326=)
 ClinVar dbSNP
3g.30672266C>TCA432917571TGFBR2c.1083C>T (p.Leu361=)
n.2679C>T
c.1158C>T (p.Leu386=)
c.1110C>T (p.Leu370=)
c.1035C>T (p.Leu345=)
c.978C>T (p.Leu326=)
 dbSNP gnomAD v4
3g.30672267C>ACA351808500TGFBR2c.1084C>A (p.His362Asn)
n.2680C>A
c.1159C>A (p.His387Asn)
c.1111C>A (p.His371Asn)
c.1036C>A (p.His346Asn)
c.979C>A (p.His327Asn)
 dbSNP
3g.30672267C>GCA351808499TGFBR2c.1084C>G (p.His362Asp)
n.2680C>G
c.1159C>G (p.His387Asp)
c.1111C>G (p.His371Asp)
c.1036C>G (p.His346Asp)
c.979C>G (p.His327Asp)
3g.30672267C>TCA351808498TGFBR2c.1084C>T (p.His362Tyr)
n.2680C>T
c.1159C>T (p.His387Tyr)
c.1111C>T (p.His371Tyr)
c.1036C>T (p.His346Tyr)
c.979C>T (p.His327Tyr)
 dbSNP COSMIC COSMIC
3g.30672268A=CA1354873214TGFBR2c.1085A= (p.His362=)
n.2681A=
c.1160A= (p.His387=)
c.1112A= (p.His371=)
c.1037A= (p.His346=)
c.980A= (p.His327=)
3g.30672268A>CCA351808501TGFBR2c.1085A>C (p.His362Pro)
n.2681A>C
c.1160A>C (p.His387Pro)
c.1112A>C (p.His371Pro)
c.1037A>C (p.His346Pro)
c.980A>C (p.His327Pro)
 dbSNP
3g.30672268A>GCA324658TGFBR2c.1085A>G (p.His362Arg)
n.2681A>G
c.1160A>G (p.His387Arg)
c.1112A>G (p.His371Arg)
c.1037A>G (p.His346Arg)
c.980A>G (p.His327Arg)
 ClinVar dbSNP
3g.30672268A>TCA351808502TGFBR2c.1085A>T (p.His362Leu)
n.2681A>T
c.1160A>T (p.His387Leu)
c.1112A>T (p.His371Leu)
c.1037A>T (p.His346Leu)
c.980A>T (p.His327Leu)
 dbSNP
3g.30672269C>ACA351808503TGFBR2c.1086C>A (p.His362Gln)
n.2682C>A
c.1161C>A (p.His387Gln)
c.1113C>A (p.His371Gln)
c.1038C>A (p.His346Gln)
c.981C>A (p.His327Gln)
 dbSNP
3g.30672269C>GCA351808504TGFBR2c.1086C>G (p.His362Gln)
n.2682C>G
c.1161C>G (p.His387Gln)
c.1113C>G (p.His371Gln)
c.1038C>G (p.His346Gln)
c.981C>G (p.His327Gln)
 dbSNP
3g.30672269C>TCA432917573TGFBR2c.1086C>T (p.His362=)
n.2682C>T
c.1161C>T (p.His387=)
c.1113C>T (p.His371=)
c.1038C>T (p.His346=)
c.981C>T (p.His327=)
 dbSNP gnomAD v4
3g.30672270A>CCA351808505TGFBR2c.1087A>C (p.Ser363Arg)
n.2683A>C
c.1162A>C (p.Ser388Arg)
c.1114A>C (p.Ser372Arg)
c.1039A>C (p.Ser347Arg)
c.982A>C (p.Ser328Arg)
3g.30672270A>GCA351808506TGFBR2c.1087A>G (p.Ser363Gly)
n.2683A>G
c.1162A>G (p.Ser388Gly)
c.1114A>G (p.Ser372Gly)
c.1039A>G (p.Ser347Gly)
c.982A>G (p.Ser328Gly)
 ClinVar dbSNP gnomAD v4
3g.30672270A>TCA351808507TGFBR2c.1087A>T (p.Ser363Cys)
n.2683A>T
c.1162A>T (p.Ser388Cys)
c.1114A>T (p.Ser372Cys)
c.1039A>T (p.Ser347Cys)
c.982A>T (p.Ser328Cys)
 dbSNP
3g.30672271G>ACA351808508TGFBR2c.1088G>A (p.Ser363Asn)
n.2684G>A
c.1163G>A (p.Ser388Asn)
c.1115G>A (p.Ser372Asn)
c.1040G>A (p.Ser347Asn)
c.983G>A (p.Ser328Asn)
3g.30672271G>CCA351808509TGFBR2c.1088G>C (p.Ser363Thr)
n.2684G>C
c.1163G>C (p.Ser388Thr)
c.1115G>C (p.Ser372Thr)
c.1040G>C (p.Ser347Thr)
c.983G>C (p.Ser328Thr)
3g.30672271G>TCA351808510TGFBR2c.1088G>T (p.Ser363Ile)
n.2684G>T
c.1163G>T (p.Ser388Ile)
c.1115G>T (p.Ser372Ile)
c.1040G>T (p.Ser347Ile)
c.983G>T (p.Ser328Ile)
3g.30672272T>ACA351808511TGFBR2c.1089T>A (p.Ser363Arg)
n.2685T>A
c.1164T>A (p.Ser388Arg)
c.1116T>A (p.Ser372Arg)
c.1041T>A (p.Ser347Arg)
c.984T>A (p.Ser328Arg)
 dbSNP
3g.30672272T>CCA432917574TGFBR2c.1089T>C (p.Ser363=)
n.2685T>C
c.1164T>C (p.Ser388=)
c.1116T>C (p.Ser372=)
c.1041T>C (p.Ser347=)
c.984T>C (p.Ser328=)
 dbSNP gnomAD v4
3g.30672272T>GCA351808512TGFBR2c.1089T>G (p.Ser363Arg)
n.2685T>G
c.1164T>G (p.Ser388Arg)
c.1116T>G (p.Ser372Arg)
c.1041T>G (p.Ser347Arg)
c.984T>G (p.Ser328Arg)
 dbSNP
3g.30672273G>ACA351808514TGFBR2c.1090G>A (p.Asp364Asn)
n.2686G>A
c.1165G>A (p.Asp389Asn)
c.1117G>A (p.Asp373Asn)
c.1042G>A (p.Asp348Asn)
c.985G>A (p.Asp329Asn)
 dbSNP COSMIC COSMIC
3g.30672273G>CCA351808515TGFBR2c.1090G>C (p.Asp364His)
n.2686G>C
c.1165G>C (p.Asp389His)
c.1117G>C (p.Asp373His)
c.1042G>C (p.Asp348His)
c.985G>C (p.Asp329His)
 dbSNP gnomAD v2 gnomAD v4
3g.30672273G=CA1354873215TGFBR2c.1090G= (p.Asp364=)
n.2686G=
c.1165G= (p.Asp389=)
c.1117G= (p.Asp373=)
c.1042G= (p.Asp348=)
c.985G= (p.Asp329=)
3g.30672273G>TCA351808513TGFBR2c.1090G>T (p.Asp364Tyr)
n.2686G>T
c.1165G>T (p.Asp389Tyr)
c.1117G>T (p.Asp373Tyr)
c.1042G>T (p.Asp348Tyr)
c.985G>T (p.Asp329Tyr)
 dbSNP
3g.30672274A=CA1354873216TGFBR2c.1091A= (p.Asp364=)
n.2687A=
c.1166A= (p.Asp389=)
c.1118A= (p.Asp373=)
c.1043A= (p.Asp348=)
c.986A= (p.Asp329=)
3g.30672274A>CCA351808516TGFBR2c.1091A>C (p.Asp364Ala)
n.2687A>C
c.1166A>C (p.Asp389Ala)
c.1118A>C (p.Asp373Ala)
c.1043A>C (p.Asp348Ala)
c.986A>C (p.Asp329Ala)
 dbSNP
3g.30672274A>GCA351808517TGFBR2c.1091A>G (p.Asp364Gly)
n.2687A>G
c.1166A>G (p.Asp389Gly)
c.1118A>G (p.Asp373Gly)
c.1043A>G (p.Asp348Gly)
c.986A>G (p.Asp329Gly)
 dbSNP
3g.30672274A>TCA351808518TGFBR2c.1091A>T (p.Asp364Val)
n.2687A>T
c.1166A>T (p.Asp389Val)
c.1118A>T (p.Asp373Val)
c.1043A>T (p.Asp348Val)
c.986A>T (p.Asp329Val)
 dbSNP
3g.30672275T>ACA351808519TGFBR2c.1092T>A (p.Asp364Glu)
n.2688T>A
c.1167T>A (p.Asp389Glu)
c.1119T>A (p.Asp373Glu)
c.1044T>A (p.Asp348Glu)
c.987T>A (p.Asp329Glu)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
3g.30672275T>CCA045631TGFBR2c.1092T>C (p.Asp364=)
n.2688T>C
c.1167T>C (p.Asp389=)
c.1119T>C (p.Asp373=)
c.1044T>C (p.Asp348=)
c.987T>C (p.Asp329=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672275T>GCA351808520TGFBR2c.1092T>G (p.Asp364Glu)
n.2688T>G
c.1167T>G (p.Asp389Glu)
c.1119T>G (p.Asp373Glu)
c.1044T>G (p.Asp348Glu)
c.987T>G (p.Asp329Glu)
 dbSNP
3g.30672275T=CA1354873217TGFBR2c.1092T= (p.Asp364=)
n.2688T=
c.1167T= (p.Asp389=)
c.1119T= (p.Asp373=)
c.1044T= (p.Asp348=)
c.987T= (p.Asp329=)
3g.30672276C>ACA351808521TGFBR2c.1093C>A (p.His365Asn)
n.2689C>A
c.1168C>A (p.His390Asn)
c.1120C>A (p.His374Asn)
c.1045C>A (p.His349Asn)
c.988C>A (p.His330Asn)
 dbSNP
3g.30672276C>GCA351808522TGFBR2c.1093C>G (p.His365Asp)
n.2689C>G
c.1168C>G (p.His390Asp)
c.1120C>G (p.His374Asp)
c.1045C>G (p.His349Asp)
c.988C>G (p.His330Asp)
 dbSNP COSMIC COSMIC
3g.30672276C>TCA351808523TGFBR2c.1093C>T (p.His365Tyr)
n.2689C>T
c.1168C>T (p.His390Tyr)
c.1120C>T (p.His374Tyr)
c.1045C>T (p.His349Tyr)
c.988C>T (p.His330Tyr)
 dbSNP
3g.30672277A>CCA351808524TGFBR2c.1094A>C (p.His365Pro)
n.2690A>C
c.1169A>C (p.His390Pro)
c.1121A>C (p.His374Pro)
c.1046A>C (p.His349Pro)
c.989A>C (p.His330Pro)
3g.30672277A>GCA351808525TGFBR2c.1094A>G (p.His365Arg)
n.2690A>G
c.1169A>G (p.His390Arg)
c.1121A>G (p.His374Arg)
c.1046A>G (p.His349Arg)
c.989A>G (p.His330Arg)
 dbSNP
3g.30672277A>TCA351808526TGFBR2c.1094A>T (p.His365Leu)
n.2690A>T
c.1169A>T (p.His390Leu)
c.1121A>T (p.His374Leu)
c.1046A>T (p.His349Leu)
c.989A>T (p.His330Leu)
 dbSNP
3g.30672278C>ACA351808527TGFBR2c.1095C>A (p.His365Gln)
n.2691C>A
c.1170C>A (p.His390Gln)
c.1122C>A (p.His374Gln)
c.1047C>A (p.His349Gln)
c.990C>A (p.His330Gln)
 dbSNP
3g.30672278C>GCA351808528TGFBR2c.1095C>G (p.His365Gln)
n.2691C>G
c.1170C>G (p.His390Gln)
c.1122C>G (p.His374Gln)
c.1047C>G (p.His349Gln)
c.990C>G (p.His330Gln)
 dbSNP gnomAD v4
3g.30672278C>TCA432917575TGFBR2c.1095C>T (p.His365=)
n.2691C>T
c.1170C>T (p.His390=)
c.1122C>T (p.His374=)
c.1047C>T (p.His349=)
c.990C>T (p.His330=)
3g.30672279A=CA1354873218TGFBR2c.1096A= (p.Thr366=)
n.2692A=
c.1171A= (p.Thr391=)
c.1123A= (p.Thr375=)
c.1048A= (p.Thr350=)
c.991A= (p.Thr331=)
3g.30672279A>CCA351808530TGFBR2c.1096A>C (p.Thr366Pro)
n.2692A>C
c.1171A>C (p.Thr391Pro)
c.1123A>C (p.Thr375Pro)
c.1048A>C (p.Thr350Pro)
c.991A>C (p.Thr331Pro)
 dbSNP
3g.30672279A>GCA045643TGFBR2c.1096A>G (p.Thr366Ala)
n.2692A>G
c.1171A>G (p.Thr391Ala)
c.1123A>G (p.Thr375Ala)
c.1048A>G (p.Thr350Ala)
c.991A>G (p.Thr331Ala)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672279A>TCA351808529TGFBR2c.1096A>T (p.Thr366Ser)
n.2692A>T
c.1171A>T (p.Thr391Ser)
c.1123A>T (p.Thr375Ser)
c.1048A>T (p.Thr350Ser)
c.991A>T (p.Thr331Ser)
 dbSNP
3g.30672280C>ACA351808531TGFBR2c.1097C>A (p.Thr366Asn)
n.2693C>A
c.1172C>A (p.Thr391Asn)
c.1124C>A (p.Thr375Asn)
c.1049C>A (p.Thr350Asn)
c.992C>A (p.Thr331Asn)
 dbSNP gnomAD v4
3g.30672280C=CA1354873219TGFBR2c.1097C= (p.Thr366=)
n.2693C=
c.1172C= (p.Thr391=)
c.1124C= (p.Thr375=)
c.1049C= (p.Thr350=)
c.992C= (p.Thr331=)
3g.30672280C>GCA351808532TGFBR2c.1097C>G (p.Thr366Ser)
n.2693C>G
c.1172C>G (p.Thr391Ser)
c.1124C>G (p.Thr375Ser)
c.1049C>G (p.Thr350Ser)
c.992C>G (p.Thr331Ser)
 dbSNP
3g.30672280C>TCA351808533TGFBR2c.1097C>T (p.Thr366Ile)
n.2693C>T
c.1172C>T (p.Thr391Ile)
c.1124C>T (p.Thr375Ile)
c.1049C>T (p.Thr350Ile)
c.992C>T (p.Thr331Ile)
 ClinVar dbSNP gnomAD v4
3g.30672281T>ACA432917578TGFBR2c.1098T>A (p.Thr366=)
n.2694T>A
c.1173T>A (p.Thr391=)
c.1125T>A (p.Thr375=)
c.1050T>A (p.Thr350=)
c.993T>A (p.Thr331=)
 COSMIC COSMIC
3g.30672281T>CCA432917576TGFBR2c.1098T>C (p.Thr366=)
n.2694T>C
c.1173T>C (p.Thr391=)
c.1125T>C (p.Thr375=)
c.1050T>C (p.Thr350=)
c.993T>C (p.Thr331=)
3g.30672281T>GCA432917577TGFBR2c.1098T>G (p.Thr366=)
n.2694T>G
c.1173T>G (p.Thr391=)
c.1125T>G (p.Thr375=)
c.1050T>G (p.Thr350=)
c.993T>G (p.Thr331=)
3g.30672282C>ACA351808534TGFBR2c.1099C>A (p.Pro367Thr)
n.2695C>A
c.1174C>A (p.Pro392Thr)
c.1126C>A (p.Pro376Thr)
c.1051C>A (p.Pro351Thr)
c.994C>A (p.Pro332Thr)
 dbSNP gnomAD v4
3g.30672282C>GCA351808535TGFBR2c.1099C>G (p.Pro367Ala)
n.2695C>G
c.1174C>G (p.Pro392Ala)
c.1126C>G (p.Pro376Ala)
c.1051C>G (p.Pro351Ala)
c.994C>G (p.Pro332Ala)
3g.30672282C>TCA351808536TGFBR2c.1099C>T (p.Pro367Ser)
n.2695C>T
c.1174C>T (p.Pro392Ser)
c.1126C>T (p.Pro376Ser)
c.1051C>T (p.Pro351Ser)
c.994C>T (p.Pro332Ser)
3g.30672283C>ACA351808537TGFBR2c.1100C>A (p.Pro367Gln)
n.2696C>A
c.1175C>A (p.Pro392Gln)
c.1127C>A (p.Pro376Gln)
c.1052C>A (p.Pro351Gln)
c.995C>A (p.Pro332Gln)
 dbSNP
3g.30672283C=CA1354873220TGFBR2c.1100C= (p.Pro367=)
n.2696C=
c.1175C= (p.Pro392=)
c.1127C= (p.Pro376=)
c.1052C= (p.Pro351=)
c.995C= (p.Pro332=)
3g.30672283C>GCA351808538TGFBR2c.1100C>G (p.Pro367Arg)
n.2696C>G
c.1175C>G (p.Pro392Arg)
c.1127C>G (p.Pro376Arg)
c.1052C>G (p.Pro351Arg)
c.995C>G (p.Pro332Arg)
 dbSNP
3g.30672283C>TCA351808539TGFBR2c.1100C>T (p.Pro367Leu)
n.2696C>T
c.1175C>T (p.Pro392Leu)
c.1127C>T (p.Pro376Leu)
c.1052C>T (p.Pro351Leu)
c.995C>T (p.Pro332Leu)
 ClinVar dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC
3g.30672284A=CA1354873221TGFBR2c.1101A= (p.Pro367=)
n.2697A=
c.1176A= (p.Pro392=)
c.1128A= (p.Pro376=)
c.1053A= (p.Pro351=)
c.996A= (p.Pro332=)
3g.30672284A>CCA432917579TGFBR2c.1101A>C (p.Pro367=)
n.2697A>C
c.1176A>C (p.Pro392=)
c.1128A>C (p.Pro376=)
c.1053A>C (p.Pro351=)
c.996A>C (p.Pro332=)
 dbSNP
3g.30672284A>GCA045668TGFBR2c.1101A>G (p.Pro367=)
n.2697A>G
c.1176A>G (p.Pro392=)
c.1128A>G (p.Pro376=)
c.1053A>G (p.Pro351=)
c.996A>G (p.Pro332=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672284A>TCA432917580TGFBR2c.1101A>T (p.Pro367=)
n.2697A>T
c.1176A>T (p.Pro392=)
c.1128A>T (p.Pro376=)
c.1053A>T (p.Pro351=)
c.996A>T (p.Pro332=)
 dbSNP
3g.30672285T>ACA351808540TGFBR2c.1102T>A (p.Cys368Ser)
n.2698T>A
c.1177T>A (p.Cys393Ser)
c.1129T>A (p.Cys377Ser)
c.1054T>A (p.Cys352Ser)
c.997T>A (p.Cys333Ser)
 ClinVar dbSNP
3g.30672285T>CCA351808541TGFBR2c.1102T>C (p.Cys368Arg)
n.2698T>C
c.1177T>C (p.Cys393Arg)
c.1129T>C (p.Cys377Arg)
c.1054T>C (p.Cys352Arg)
c.997T>C (p.Cys333Arg)
 ClinVar dbSNP
3g.30672285T>GCA351808542TGFBR2c.1102T>G (p.Cys368Gly)
n.2698T>G
c.1177T>G (p.Cys393Gly)
c.1129T>G (p.Cys377Gly)
c.1054T>G (p.Cys352Gly)
c.997T>G (p.Cys333Gly)
 dbSNP
3g.30672286G>ACA351808543TGFBR2c.1103G>A (p.Cys368Tyr)
n.2699G>A
c.1178G>A (p.Cys393Tyr)
c.1130G>A (p.Cys377Tyr)
c.1055G>A (p.Cys352Tyr)
c.998G>A (p.Cys333Tyr)
 dbSNP gnomAD v4
3g.30672286G>CCA351808545TGFBR2c.1103G>C (p.Cys368Ser)
n.2699G>C
c.1178G>C (p.Cys393Ser)
c.1130G>C (p.Cys377Ser)
c.1055G>C (p.Cys352Ser)
c.998G>C (p.Cys333Ser)
 dbSNP
3g.30672286G>TCA351808544TGFBR2c.1103G>T (p.Cys368Phe)
n.2699G>T
c.1178G>T (p.Cys393Phe)
c.1130G>T (p.Cys377Phe)
c.1055G>T (p.Cys352Phe)
c.998G>T (p.Cys333Phe)
3g.30672287T>ACA351808546TGFBR2c.1104T>A (p.Cys368Ter)
n.2700T>A
c.1179T>A (p.Cys393Ter)
c.1131T>A (p.Cys377Ter)
c.1056T>A (p.Cys352Ter)
c.999T>A (p.Cys333Ter)
3g.30672287T>CCA432917581TGFBR2c.1104T>C (p.Cys368=)
n.2700T>C
c.1179T>C (p.Cys393=)
c.1131T>C (p.Cys377=)
c.1056T>C (p.Cys352=)
c.999T>C (p.Cys333=)
3g.30672287T>GCA351808547TGFBR2c.1104T>G (p.Cys368Trp)
n.2700T>G
c.1179T>G (p.Cys393Trp)
c.1131T>G (p.Cys377Trp)
c.1056T>G (p.Cys352Trp)
c.999T>G (p.Cys333Trp)
3g.30672288G>ACA351808548TGFBR2c.1105G>A (p.Gly369Arg)
n.2701G>A
c.1180G>A (p.Gly394Arg)
c.1132G>A (p.Gly378Arg)
c.1057G>A (p.Gly353Arg)
c.1000G>A (p.Gly334Arg)
 dbSNP
3g.30672288G>CCA045693TGFBR2c.1105G>C (p.Gly369Arg)
n.2701G>C
c.1180G>C (p.Gly394Arg)
c.1132G>C (p.Gly378Arg)
c.1057G>C (p.Gly353Arg)
c.1000G>C (p.Gly334Arg)
 dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672288G=CA1354873222TGFBR2c.1105G= (p.Gly369=)
n.2701G=
c.1180G= (p.Gly394=)
c.1132G= (p.Gly378=)
c.1057G= (p.Gly353=)
c.1000G= (p.Gly334=)
3g.30672288G>TCA351808549TGFBR2c.1105G>T (p.Gly369Trp)
n.2701G>T
c.1180G>T (p.Gly394Trp)
c.1132G>T (p.Gly378Trp)
c.1057G>T (p.Gly353Trp)
c.1000G>T (p.Gly334Trp)
 dbSNP gnomAD v2 gnomAD v4
3g.30672290delCA2702373804TGFBR2c.1107del (p.Arg370GlyfsTer18)
n.2703del
c.1182del (p.Arg395GlyfsTer18)
c.1134del (p.Arg379GlyfsTer18)
c.1059del (p.Arg354GlyfsTer18)
c.1002del (p.Arg335GlyfsTer18)
 dbSNP

Number of alleles fetched