Chr Mutation (hg38) CAid Gene Transcript Linkouts
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
3g.30672289G>ACA351808550TGFBR2c.1106G>A (p.Gly369Glu)
n.2702G>A
c.1181G>A (p.Gly394Glu)
c.1133G>A (p.Gly378Glu)
c.1058G>A (p.Gly353Glu)
c.1001G>A (p.Gly334Glu)
 dbSNP gnomAD v4
3g.30672289G>CCA351808552TGFBR2c.1106G>C (p.Gly369Ala)
n.2702G>C
c.1181G>C (p.Gly394Ala)
c.1133G>C (p.Gly378Ala)
c.1058G>C (p.Gly353Ala)
c.1001G>C (p.Gly334Ala)
 dbSNP
3g.30672289G>TCA351808551TGFBR2c.1106G>T (p.Gly369Val)
n.2702G>T
c.1181G>T (p.Gly394Val)
c.1133G>T (p.Gly378Val)
c.1058G>T (p.Gly353Val)
c.1001G>T (p.Gly334Val)
 dbSNP
3g.30672290G>ACA71528749TGFBR2c.1107G>A (p.Gly369=)
n.2703G>A
c.1182G>A (p.Gly394=)
c.1134G>A (p.Gly378=)
c.1059G>A (p.Gly353=)
c.1002G>A (p.Gly334=)
 dbSNP gnomAD v4
3g.30672290G>CCA432917583TGFBR2c.1107G>C (p.Gly369=)
n.2703G>C
c.1182G>C (p.Gly394=)
c.1134G>C (p.Gly378=)
c.1059G>C (p.Gly353=)
c.1002G>C (p.Gly334=)
 dbSNP
3g.30672290G=CA1354873223TGFBR2c.1107G= (p.Gly369=)
n.2703G=
c.1182G= (p.Gly394=)
c.1134G= (p.Gly378=)
c.1059G= (p.Gly353=)
c.1002G= (p.Gly334=)
3g.30672290G>TCA432917582TGFBR2c.1107G>T (p.Gly369=)
n.2703G>T
c.1182G>T (p.Gly394=)
c.1134G>T (p.Gly378=)
c.1059G>T (p.Gly353=)
c.1002G>T (p.Gly334=)
3g.30672291A>CCA432917584TGFBR2c.1108A>C (p.Arg370=)
n.2704A>C
c.1183A>C (p.Arg395=)
c.1135A>C (p.Arg379=)
c.1060A>C (p.Arg354=)
c.1003A>C (p.Arg335=)
3g.30672291A>GCA351808553TGFBR2c.1108A>G (p.Arg370Gly)
n.2704A>G
c.1183A>G (p.Arg395Gly)
c.1135A>G (p.Arg379Gly)
c.1060A>G (p.Arg354Gly)
c.1003A>G (p.Arg335Gly)
 dbSNP
3g.30672291A>TCA351808554TGFBR2c.1108A>T (p.Arg370Trp)
n.2704A>T
c.1183A>T (p.Arg395Trp)
c.1135A>T (p.Arg379Trp)
c.1060A>T (p.Arg354Trp)
c.1003A>T (p.Arg335Trp)
 dbSNP
3g.30672292G>ACA351808555TGFBR2c.1109G>A (p.Arg370Lys)
n.2705G>A
c.1184G>A (p.Arg395Lys)
c.1136G>A (p.Arg379Lys)
c.1061G>A (p.Arg354Lys)
c.1004G>A (p.Arg335Lys)
 dbSNP gnomAD v2 gnomAD v4
3g.30672292G>CCA351808556TGFBR2c.1109G>C (p.Arg370Thr)
n.2705G>C
c.1184G>C (p.Arg395Thr)
c.1136G>C (p.Arg379Thr)
c.1061G>C (p.Arg354Thr)
c.1004G>C (p.Arg335Thr)
 ClinVar dbSNP
3g.30672292G=CA1354873224TGFBR2c.1109G= (p.Arg370=)
n.2705G=
c.1184G= (p.Arg395=)
c.1136G= (p.Arg379=)
c.1061G= (p.Arg354=)
c.1004G= (p.Arg335=)
3g.30672292G>TCA045705TGFBR2c.1109G>T (p.Arg370Met)
n.2705G>T
c.1184G>T (p.Arg395Met)
c.1136G>T (p.Arg379Met)
c.1061G>T (p.Arg354Met)
c.1004G>T (p.Arg335Met)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672293G>ACA432917585TGFBR2c.1110G>A (p.Arg370=)
n.2706G>A
c.1185G>A (p.Arg395=)
c.1137G>A (p.Arg379=)
c.1062G>A (p.Arg354=)
c.1005G>A (p.Arg335=)
3g.30672293G>CCA351808557TGFBR2c.1110G>C (p.Arg370Ser)
n.2706G>C
c.1185G>C (p.Arg395Ser)
c.1137G>C (p.Arg379Ser)
c.1062G>C (p.Arg354Ser)
c.1005G>C (p.Arg335Ser)
 ClinVar
3g.30672293G>TCA351808558TGFBR2c.1110G>T (p.Arg370Ser)
n.2706G>T
c.1185G>T (p.Arg395Ser)
c.1137G>T (p.Arg379Ser)
c.1062G>T (p.Arg354Ser)
c.1005G>T (p.Arg335Ser)
3g.30672294C>ACA351808559TGFBR2c.1111C>A (p.Pro371Thr)
n.2707C>A
c.1186C>A (p.Pro396Thr)
c.1138C>A (p.Pro380Thr)
c.1063C>A (p.Pro355Thr)
c.1006C>A (p.Pro336Thr)
 dbSNP gnomAD v4
3g.30672294C>GCA351808560TGFBR2c.1111C>G (p.Pro371Ala)
n.2707C>G
c.1186C>G (p.Pro396Ala)
c.1138C>G (p.Pro380Ala)
c.1063C>G (p.Pro355Ala)
c.1006C>G (p.Pro336Ala)
 dbSNP
3g.30672294C>TCA351808561TGFBR2c.1111C>T (p.Pro371Ser)
n.2707C>T
c.1186C>T (p.Pro396Ser)
c.1138C>T (p.Pro380Ser)
c.1063C>T (p.Pro355Ser)
c.1006C>T (p.Pro336Ser)
 dbSNP
3g.30672295C>ACA351808562TGFBR2c.1112C>A (p.Pro371His)
n.2708C>A
c.1187C>A (p.Pro396His)
c.1139C>A (p.Pro380His)
c.1064C>A (p.Pro355His)
c.1007C>A (p.Pro336His)
 dbSNP
3g.30672295C>GCA351808563TGFBR2c.1112C>G (p.Pro371Arg)
n.2708C>G
c.1187C>G (p.Pro396Arg)
c.1139C>G (p.Pro380Arg)
c.1064C>G (p.Pro355Arg)
c.1007C>G (p.Pro336Arg)
 dbSNP
3g.30672295C>TCA351808564TGFBR2c.1112C>T (p.Pro371Leu)
n.2708C>T
c.1187C>T (p.Pro396Leu)
c.1139C>T (p.Pro380Leu)
c.1064C>T (p.Pro355Leu)
c.1007C>T (p.Pro336Leu)
 dbSNP
3g.30672296C>ACA432917586TGFBR2c.1113C>A (p.Pro371=)
n.2709C>A
c.1188C>A (p.Pro396=)
c.1140C>A (p.Pro380=)
c.1065C>A (p.Pro355=)
c.1008C>A (p.Pro336=)
 dbSNP gnomAD v2 gnomAD v4
3g.30672296C=CA1354873225TGFBR2c.1113C= (p.Pro371=)
n.2709C=
c.1188C= (p.Pro396=)
c.1140C= (p.Pro380=)
c.1065C= (p.Pro355=)
c.1008C= (p.Pro336=)
3g.30672296C>GCA432917587TGFBR2c.1113C>G (p.Pro371=)
n.2709C>G
c.1188C>G (p.Pro396=)
c.1140C>G (p.Pro380=)
c.1065C>G (p.Pro355=)
c.1008C>G (p.Pro336=)
 ClinVar dbSNP
3g.30672296C>TCA432917588TGFBR2c.1113C>T (p.Pro371=)
n.2709C>T
c.1188C>T (p.Pro396=)
c.1140C>T (p.Pro380=)
c.1065C>T (p.Pro355=)
c.1008C>T (p.Pro336=)
 dbSNP
3g.30672297A>CCA351808565TGFBR2c.1114A>C (p.Lys372Gln)
n.2710A>C
c.1189A>C (p.Lys397Gln)
c.1141A>C (p.Lys381Gln)
c.1066A>C (p.Lys356Gln)
c.1009A>C (p.Lys337Gln)
3g.30672297A>GCA351808566TGFBR2c.1114A>G (p.Lys372Glu)
n.2710A>G
c.1189A>G (p.Lys397Glu)
c.1141A>G (p.Lys381Glu)
c.1066A>G (p.Lys356Glu)
c.1009A>G (p.Lys337Glu)
 ClinVar dbSNP
3g.30672297A>TCA351808567TGFBR2c.1114A>T (p.Lys372Ter)
n.2710A>T
c.1189A>T (p.Lys397Ter)
c.1141A>T (p.Lys381Ter)
c.1066A>T (p.Lys356Ter)
c.1009A>T (p.Lys337Ter)
 dbSNP
3g.30672298A=CA1354873226TGFBR2c.1115A= (p.Lys372=)
n.2711A=
c.1190A= (p.Lys397=)
c.1142A= (p.Lys381=)
c.1067A= (p.Lys356=)
c.1010A= (p.Lys337=)
3g.30672298A>CCA351808568TGFBR2c.1115A>C (p.Lys372Thr)
n.2711A>C
c.1190A>C (p.Lys397Thr)
c.1142A>C (p.Lys381Thr)
c.1067A>C (p.Lys356Thr)
c.1010A>C (p.Lys337Thr)
3g.30672298A>GCA351808569TGFBR2c.1115A>G (p.Lys372Arg)
n.2711A>G
c.1190A>G (p.Lys397Arg)
c.1142A>G (p.Lys381Arg)
c.1067A>G (p.Lys356Arg)
c.1010A>G (p.Lys337Arg)
 ClinVar dbSNP gnomAD v3 gnomAD v4
3g.30672298A>TCA351808570TGFBR2c.1115A>T (p.Lys372Met)
n.2711A>T
c.1190A>T (p.Lys397Met)
c.1142A>T (p.Lys381Met)
c.1067A>T (p.Lys356Met)
c.1010A>T (p.Lys337Met)
 dbSNP
3g.30672298_30672299insAGTGCTGCA2702373825TGFBR2c.1115_1116insAGTGCTG (p.Met373ValfsTer27)
n.2711_2712insAGTGCTG
c.1190_1191insAGTGCTG (p.Met398ValfsTer27)
c.1142_1143insAGTGCTG (p.Met382ValfsTer27)
c.1067_1068insAGTGCTG (p.Met357ValfsTer27)
c.1010_1011insAGTGCTG (p.Met338ValfsTer27)
 dbSNP
3g.30672299G>ACA045718TGFBR2c.1116G>A (p.Lys372=)
n.2712G>A
c.1191G>A (p.Lys397=)
c.1143G>A (p.Lys381=)
c.1068G>A (p.Lys356=)
c.1011G>A (p.Lys337=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672299G>CCA351808571TGFBR2c.1116G>C (p.Lys372Asn)
n.2712G>C
c.1191G>C (p.Lys397Asn)
c.1143G>C (p.Lys381Asn)
c.1068G>C (p.Lys356Asn)
c.1011G>C (p.Lys337Asn)
 dbSNP
3g.30672299G=CA1354873227TGFBR2c.1116G= (p.Lys372=)
n.2712G=
c.1191G= (p.Lys397=)
c.1143G= (p.Lys381=)
c.1068G= (p.Lys356=)
c.1011G= (p.Lys337=)
3g.30672299G>TCA351808572TGFBR2c.1116G>T (p.Lys372Asn)
n.2712G>T
c.1191G>T (p.Lys397Asn)
c.1143G>T (p.Lys381Asn)
c.1068G>T (p.Lys356Asn)
c.1011G>T (p.Lys337Asn)
 dbSNP
3g.30672300A>CCA351808573TGFBR2c.1117A>C (p.Met373Leu)
n.2713A>C
c.1192A>C (p.Met398Leu)
c.1144A>C (p.Met382Leu)
c.1069A>C (p.Met357Leu)
c.1012A>C (p.Met338Leu)
 dbSNP
3g.30672300A>GCA351808574TGFBR2c.1117A>G (p.Met373Val)
n.2713A>G
c.1192A>G (p.Met398Val)
c.1144A>G (p.Met382Val)
c.1069A>G (p.Met357Val)
c.1012A>G (p.Met338Val)
 ClinVar dbSNP COSMIC COSMIC
3g.30672300A>TCA351808575TGFBR2c.1117A>T (p.Met373Leu)
n.2713A>T
c.1192A>T (p.Met398Leu)
c.1144A>T (p.Met382Leu)
c.1069A>T (p.Met357Leu)
c.1012A>T (p.Met338Leu)
 dbSNP
3g.30672301T>ACA351808576TGFBR2c.1118T>A (p.Met373Lys)
n.2714T>A
c.1193T>A (p.Met398Lys)
c.1145T>A (p.Met382Lys)
c.1070T>A (p.Met357Lys)
c.1013T>A (p.Met338Lys)
 ClinVar dbSNP gnomAD v4
3g.30672301T>CCA351808577TGFBR2c.1118T>C (p.Met373Thr)
n.2714T>C
c.1193T>C (p.Met398Thr)
c.1145T>C (p.Met382Thr)
c.1070T>C (p.Met357Thr)
c.1013T>C (p.Met338Thr)
3g.30672301T>GCA351808578TGFBR2c.1118T>G (p.Met373Arg)
n.2714T>G
c.1193T>G (p.Met398Arg)
c.1145T>G (p.Met382Arg)
c.1070T>G (p.Met357Arg)
c.1013T>G (p.Met338Arg)
 dbSNP
3g.30672301T=CA1354873228TGFBR2c.1118T= (p.Met373=)
n.2714T=
c.1193T= (p.Met398=)
c.1145T= (p.Met382=)
c.1070T= (p.Met357=)
c.1013T= (p.Met338=)
3g.30672302G>ACA020605TGFBR2c.1119G>A (p.Met373Ile)
n.2715G>A
c.1194G>A (p.Met398Ile)
c.1146G>A (p.Met382Ile)
c.1071G>A (p.Met357Ile)
c.1014G>A (p.Met338Ile)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672302G>CCA351808579TGFBR2c.1119G>C (p.Met373Ile)
n.2715G>C
c.1194G>C (p.Met398Ile)
c.1146G>C (p.Met382Ile)
c.1071G>C (p.Met357Ile)
c.1014G>C (p.Met338Ile)
3g.30672302G=CA1354873229TGFBR2c.1119G= (p.Met373=)
n.2715G=
c.1194G= (p.Met398=)
c.1146G= (p.Met382=)
c.1071G= (p.Met357=)
c.1014G= (p.Met338=)
3g.30672302G>TCA351808580TGFBR2c.1119G>T (p.Met373Ile)
n.2715G>T
c.1194G>T (p.Met398Ile)
c.1146G>T (p.Met382Ile)
c.1071G>T (p.Met357Ile)
c.1014G>T (p.Met338Ile)
3g.30672303C>ACA351808581TGFBR2c.1120C>A (p.Pro374Thr)
n.2716C>A
c.1195C>A (p.Pro399Thr)
c.1147C>A (p.Pro383Thr)
c.1072C>A (p.Pro358Thr)
c.1015C>A (p.Pro339Thr)
 dbSNP
3g.30672303C=CA1354873230TGFBR2c.1120C= (p.Pro374=)
n.2716C=
c.1195C= (p.Pro399=)
c.1147C= (p.Pro383=)
c.1072C= (p.Pro358=)
c.1015C= (p.Pro339=)
3g.30672303C>GCA351808582TGFBR2c.1120C>G (p.Pro374Ala)
n.2716C>G
c.1195C>G (p.Pro399Ala)
c.1147C>G (p.Pro383Ala)
c.1072C>G (p.Pro358Ala)
c.1015C>G (p.Pro339Ala)
 dbSNP gnomAD v4
3g.30672303C>TCA320627TGFBR2c.1120C>T (p.Pro374Ser)
n.2716C>T
c.1195C>T (p.Pro399Ser)
c.1147C>T (p.Pro383Ser)
c.1072C>T (p.Pro358Ser)
c.1015C>T (p.Pro339Ser)
 ClinVar dbSNP gnomAD v4
3g.30672304C>ACA351808584TGFBR2c.1121C>A (p.Pro374His)
n.2717C>A
c.1196C>A (p.Pro399His)
c.1148C>A (p.Pro383His)
c.1073C>A (p.Pro358His)
c.1016C>A (p.Pro339His)
 dbSNP gnomAD v4 COSMIC COSMIC
3g.30672304C=CA1354873231TGFBR2c.1121C= (p.Pro374=)
n.2717C=
c.1196C= (p.Pro399=)
c.1148C= (p.Pro383=)
c.1073C= (p.Pro358=)
c.1016C= (p.Pro339=)
3g.30672304C>GCA351808583TGFBR2c.1121C>G (p.Pro374Arg)
n.2717C>G
c.1196C>G (p.Pro399Arg)
c.1148C>G (p.Pro383Arg)
c.1073C>G (p.Pro358Arg)
c.1016C>G (p.Pro339Arg)
 dbSNP
3g.30672304C>TCA16604508TGFBR2c.1121C>T (p.Pro374Leu)
n.2717C>T
c.1196C>T (p.Pro399Leu)
c.1148C>T (p.Pro383Leu)
c.1073C>T (p.Pro358Leu)
c.1016C>T (p.Pro339Leu)
 ClinVar dbSNP COSMIC COSMIC
3g.30672305C>ACA432917589TGFBR2c.1122C>A (p.Pro374=)
n.2718C>A
c.1197C>A (p.Pro399=)
c.1149C>A (p.Pro383=)
c.1074C>A (p.Pro358=)
c.1017C>A (p.Pro339=)
 dbSNP
3g.30672305C>GCA432917590TGFBR2c.1122C>G (p.Pro374=)
n.2718C>G
c.1197C>G (p.Pro399=)
c.1149C>G (p.Pro383=)
c.1074C>G (p.Pro358=)
c.1017C>G (p.Pro339=)
 dbSNP
3g.30672305C>TCA432917591TGFBR2c.1122C>T (p.Pro374=)
n.2718C>T
c.1197C>T (p.Pro399=)
c.1149C>T (p.Pro383=)
c.1074C>T (p.Pro358=)
c.1017C>T (p.Pro339=)
 gnomAD v4
3g.30672306A=CA1354873232TGFBR2c.1123A= (p.Ile375=)
n.2719A=
c.1198A= (p.Ile400=)
c.1150A= (p.Ile384=)
c.1075A= (p.Ile359=)
c.1018A= (p.Ile340=)
3g.30672306A>CCA351808586TGFBR2c.1123A>C (p.Ile375Leu)
n.2719A>C
c.1198A>C (p.Ile400Leu)
c.1150A>C (p.Ile384Leu)
c.1075A>C (p.Ile359Leu)
c.1018A>C (p.Ile340Leu)
 dbSNP
3g.30672306A>GCA71528768TGFBR2c.1123A>G (p.Ile375Val)
n.2719A>G
c.1198A>G (p.Ile400Val)
c.1150A>G (p.Ile384Val)
c.1075A>G (p.Ile359Val)
c.1018A>G (p.Ile340Val)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672306A>TCA351808585TGFBR2c.1123A>T (p.Ile375Phe)
n.2719A>T
c.1198A>T (p.Ile400Phe)
c.1150A>T (p.Ile384Phe)
c.1075A>T (p.Ile359Phe)
c.1018A>T (p.Ile340Phe)
 dbSNP
3g.30672307T>ACA351808587TGFBR2c.1124T>A (p.Ile375Asn)
n.2720T>A
c.1199T>A (p.Ile400Asn)
c.1151T>A (p.Ile384Asn)
c.1076T>A (p.Ile359Asn)
c.1019T>A (p.Ile340Asn)
 dbSNP
3g.30672307T>CCA351808588TGFBR2c.1124T>C (p.Ile375Thr)
n.2720T>C
c.1199T>C (p.Ile400Thr)
c.1151T>C (p.Ile384Thr)
c.1076T>C (p.Ile359Thr)
c.1019T>C (p.Ile340Thr)
3g.30672307T>GCA351808589TGFBR2c.1124T>G (p.Ile375Ser)
n.2720T>G
c.1199T>G (p.Ile400Ser)
c.1151T>G (p.Ile384Ser)
c.1076T>G (p.Ile359Ser)
c.1019T>G (p.Ile340Ser)
 dbSNP
3g.30672308C>ACA432917592TGFBR2c.1125C>A (p.Ile375=)
n.2721C>A
c.1200C>A (p.Ile400=)
c.1152C>A (p.Ile384=)
c.1077C>A (p.Ile359=)
c.1020C>A (p.Ile340=)
 dbSNP COSMIC COSMIC
3g.30672308C=CA1354873233TGFBR2c.1125C= (p.Ile375=)
n.2721C=
c.1200C= (p.Ile400=)
c.1152C= (p.Ile384=)
c.1077C= (p.Ile359=)
c.1020C= (p.Ile340=)
3g.30672308C>GCA351808590TGFBR2c.1125C>G (p.Ile375Met)
n.2721C>G
c.1200C>G (p.Ile400Met)
c.1152C>G (p.Ile384Met)
c.1077C>G (p.Ile359Met)
c.1020C>G (p.Ile340Met)
 dbSNP gnomAD v4
3g.30672308C>TCA045745TGFBR2c.1125C>T (p.Ile375=)
n.2721C>T
c.1200C>T (p.Ile400=)
c.1152C>T (p.Ile384=)
c.1077C>T (p.Ile359=)
c.1020C>T (p.Ile340=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672309G>ACA045758TGFBR2c.1126G>A (p.Val376Met)
n.2722G>A
c.1201G>A (p.Val401Met)
c.1153G>A (p.Val385Met)
c.1078G>A (p.Val360Met)
c.1021G>A (p.Val341Met)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
3g.30672309G>CCA351808591TGFBR2c.1126G>C (p.Val376Leu)
n.2722G>C
c.1201G>C (p.Val401Leu)
c.1153G>C (p.Val385Leu)
c.1078G>C (p.Val360Leu)
c.1021G>C (p.Val341Leu)
 ClinVar dbSNP
3g.30672309G=CA1354873234TGFBR2c.1126G= (p.Val376=)
n.2722G=
c.1201G= (p.Val401=)
c.1153G= (p.Val385=)
c.1078G= (p.Val360=)
c.1021G= (p.Val341=)
3g.30672309G>TCA351808592TGFBR2c.1126G>T (p.Val376Leu)
n.2722G>T
c.1201G>T (p.Val401Leu)
c.1153G>T (p.Val385Leu)
c.1078G>T (p.Val360Leu)
c.1021G>T (p.Val341Leu)
 ClinVar
3g.30672310T>ACA351808593TGFBR2c.1127T>A (p.Val376Glu)
n.2723T>A
c.1202T>A (p.Val401Glu)
c.1154T>A (p.Val385Glu)
c.1079T>A (p.Val360Glu)
c.1022T>A (p.Val341Glu)
 dbSNP
3g.30672310T>CCA351808594TGFBR2c.1127T>C (p.Val376Ala)
n.2723T>C
c.1202T>C (p.Val401Ala)
c.1154T>C (p.Val385Ala)
c.1079T>C (p.Val360Ala)
c.1022T>C (p.Val341Ala)
 dbSNP
3g.30672310T>GCA351808595TGFBR2c.1127T>G (p.Val376Gly)
n.2723T>G
c.1202T>G (p.Val401Gly)
c.1154T>G (p.Val385Gly)
c.1079T>G (p.Val360Gly)
c.1022T>G (p.Val341Gly)
 dbSNP
3g.30672311G>ACA16604405TGFBR2c.1128G>A (p.Val376=)
n.2724G>A
c.1203G>A (p.Val401=)
c.1155G>A (p.Val385=)
c.1080G>A (p.Val360=)
c.1023G>A (p.Val341=)
 ClinVar dbSNP gnomAD v4
3g.30672311G>CCA432917593TGFBR2c.1128G>C (p.Val376=)
n.2724G>C
c.1203G>C (p.Val401=)
c.1155G>C (p.Val385=)
c.1080G>C (p.Val360=)
c.1023G>C (p.Val341=)
 dbSNP
3g.30672311G=CA1354873235TGFBR2c.1128G= (p.Val376=)
n.2724G=
c.1203G= (p.Val401=)
c.1155G= (p.Val385=)
c.1080G= (p.Val360=)
c.1023G= (p.Val341=)
3g.30672311G>TCA432917594TGFBR2c.1128G>T (p.Val376=)
n.2724G>T
c.1203G>T (p.Val401=)
c.1155G>T (p.Val385=)
c.1080G>T (p.Val360=)
c.1023G>T (p.Val341=)
3g.30672312delCA2580069247TGFBR2c.1129del (p.His377ThrfsTer11)
n.2725del
c.1204del (p.His402ThrfsTer11)
c.1156del (p.His386ThrfsTer11)
c.1081del (p.His361ThrfsTer11)
c.1024del (p.His342ThrfsTer11)
 ClinVar gnomAD v4
3g.30672312C>ACA351808598TGFBR2c.1129C>A (p.His377Asn)
n.2725C>A
c.1204C>A (p.His402Asn)
c.1156C>A (p.His386Asn)
c.1081C>A (p.His361Asn)
c.1024C>A (p.His342Asn)
 dbSNP
3g.30672312C>GCA351808596TGFBR2c.1129C>G (p.His377Asp)
n.2725C>G
c.1204C>G (p.His402Asp)
c.1156C>G (p.His386Asp)
c.1081C>G (p.His361Asp)
c.1024C>G (p.His342Asp)
 ClinVar dbSNP
3g.30672312C>TCA351808597TGFBR2c.1129C>T (p.His377Tyr)
n.2725C>T
c.1204C>T (p.His402Tyr)
c.1156C>T (p.His386Tyr)
c.1081C>T (p.His361Tyr)
c.1024C>T (p.His342Tyr)
 dbSNP
3g.30672313A=CA1354873236TGFBR2c.1130A= (p.His377=)
n.2726A=
c.1205A= (p.His402=)
c.1157A= (p.His386=)
c.1082A= (p.His361=)
c.1025A= (p.His342=)
3g.30672313A>CCA351808599TGFBR2c.1130A>C (p.His377Pro)
n.2726A>C
c.1205A>C (p.His402Pro)
c.1157A>C (p.His386Pro)
c.1082A>C (p.His361Pro)
c.1025A>C (p.His342Pro)
 ClinVar dbSNP
3g.30672313A>GCA351808600TGFBR2c.1130A>G (p.His377Arg)
n.2726A>G
c.1205A>G (p.His402Arg)
c.1157A>G (p.His386Arg)
c.1082A>G (p.His361Arg)
c.1025A>G (p.His342Arg)
 ClinVar dbSNP
3g.30672313A>TCA351808601TGFBR2c.1130A>T (p.His377Leu)
n.2726A>T
c.1205A>T (p.His402Leu)
c.1157A>T (p.His386Leu)
c.1082A>T (p.His361Leu)
c.1025A>T (p.His342Leu)
 dbSNP
3g.30672314C>ACA351808602TGFBR2c.1131C>A (p.His377Gln)
n.2727C>A
c.1206C>A (p.His402Gln)
c.1158C>A (p.His386Gln)
c.1083C>A (p.His361Gln)
c.1026C>A (p.His342Gln)
 dbSNP
3g.30672314C>GCA351808603TGFBR2c.1131C>G (p.His377Gln)
n.2727C>G
c.1206C>G (p.His402Gln)
c.1158C>G (p.His386Gln)
c.1083C>G (p.His361Gln)
c.1026C>G (p.His342Gln)
 dbSNP
3g.30672314C>TCA432917595TGFBR2c.1131C>T (p.His377=)
n.2727C>T
c.1206C>T (p.His402=)
c.1158C>T (p.His386=)
c.1083C>T (p.His361=)
c.1026C>T (p.His342=)
 dbSNP COSMIC COSMIC
3g.30672315A>CCA432917596TGFBR2c.1132A>C (p.Arg378=)
n.2728A>C
c.1207A>C (p.Arg403=)
c.1159A>C (p.Arg387=)
c.1084A>C (p.Arg362=)
c.1027A>C (p.Arg343=)
 gnomAD v4
3g.30672315A>GCA351808604TGFBR2c.1132A>G (p.Arg378Gly)
n.2728A>G
c.1207A>G (p.Arg403Gly)
c.1159A>G (p.Arg387Gly)
c.1084A>G (p.Arg362Gly)
c.1027A>G (p.Arg343Gly)
 COSMIC COSMIC
3g.30672315A>TCA351808605TGFBR2c.1132A>T (p.Arg378Trp)
n.2728A>T
c.1207A>T (p.Arg403Trp)
c.1159A>T (p.Arg387Trp)
c.1084A>T (p.Arg362Trp)
c.1027A>T (p.Arg343Trp)
3g.30672316G>ACA351808606TGFBR2c.1133G>A (p.Arg378Lys)
n.2729G>A
c.1208G>A (p.Arg403Lys)
c.1160G>A (p.Arg387Lys)
c.1085G>A (p.Arg362Lys)
c.1028G>A (p.Arg343Lys)
 ClinVar dbSNP
3g.30672316G>CCA351808607TGFBR2c.1133G>C (p.Arg378Thr)
n.2729G>C
c.1208G>C (p.Arg403Thr)
c.1160G>C (p.Arg387Thr)
c.1085G>C (p.Arg362Thr)
c.1028G>C (p.Arg343Thr)
 dbSNP
3g.30672316G>TCA351808608TGFBR2c.1133G>T (p.Arg378Met)
n.2729G>T
c.1208G>T (p.Arg403Met)
c.1160G>T (p.Arg387Met)
c.1085G>T (p.Arg362Met)
c.1028G>T (p.Arg343Met)
 dbSNP COSMIC
3g.30672317G>ACA432917597TGFBR2c.1134G>A (p.Arg378=)
n.2730G>A
c.1209G>A (p.Arg403=)
c.1161G>A (p.Arg387=)
c.1086G>A (p.Arg362=)
c.1029G>A (p.Arg343=)
 ClinVar dbSNP
3g.30672317G>CCA351808609TGFBR2c.1134G>C (p.Arg378Ser)
n.2730G>C
c.1209G>C (p.Arg403Ser)
c.1161G>C (p.Arg387Ser)
c.1086G>C (p.Arg362Ser)
c.1029G>C (p.Arg343Ser)
 ClinVar dbSNP
3g.30672317G=CA1354873238TGFBR2c.1134G= (p.Arg378=)
n.2730G=
c.1209G= (p.Arg403=)
c.1161G= (p.Arg387=)
c.1086G= (p.Arg362=)
c.1029G= (p.Arg343=)
3g.30672317G>TCA351808610TGFBR2c.1134G>T (p.Arg378Ser)
n.2730G>T
c.1209G>T (p.Arg403Ser)
c.1161G>T (p.Arg387Ser)
c.1086G>T (p.Arg362Ser)
c.1029G>T (p.Arg343Ser)
 ClinVar dbSNP
3g.30672317_30672323delinsGGACCTCCA1354873237TGFBR2c.1134_1140delinsGGACCTC (p.Arg378=)
n.2730_2736delinsGGACCTC
c.1209_1215delinsGGACCTC (p.Arg403=)
c.1161_1167delinsGGACCTC (p.Arg387=)
c.1086_1092delinsGGACCTC (p.Arg362=)
c.1029_1035delinsGGACCTC (p.Arg343=)
3g.30672318G>ACA351808612TGFBR2c.1135G>A (p.Asp379Asn)
n.2731G>A
c.1210G>A (p.Asp404Asn)
c.1162G>A (p.Asp388Asn)
c.1087G>A (p.Asp363Asn)
c.1030G>A (p.Asp344Asn)
 dbSNP
3g.30672318G>CCA351808613TGFBR2c.1135G>C (p.Asp379His)
n.2731G>C
c.1210G>C (p.Asp404His)
c.1162G>C (p.Asp388His)
c.1087G>C (p.Asp363His)
c.1030G>C (p.Asp344His)
 dbSNP
3g.30672318G>TCA351808611TGFBR2c.1135G>T (p.Asp379Tyr)
n.2731G>T
c.1210G>T (p.Asp404Tyr)
c.1162G>T (p.Asp388Tyr)
c.1087G>T (p.Asp363Tyr)
c.1030G>T (p.Asp344Tyr)
 COSMIC COSMIC
3g.30672318_30672323delCA658657280TGFBR2c.1135_1140del (p.Asp379_Leu380del)
n.2731_2736del
c.1210_1215del (p.Asp404_Leu405del)
c.1162_1167del (p.Asp388_Leu389del)
c.1087_1092del (p.Asp363_Leu364del)
c.1030_1035del (p.Asp344_Leu345del)
 ClinVar dbSNP
3g.30672319A=CA1354873239TGFBR2c.1136A= (p.Asp379=)
n.2732A=
c.1211A= (p.Asp404=)
c.1163A= (p.Asp388=)
c.1088A= (p.Asp363=)
c.1031A= (p.Asp344=)
3g.30672319A>CCA351808614TGFBR2c.1136A>C (p.Asp379Ala)
n.2732A>C
c.1211A>C (p.Asp404Ala)
c.1163A>C (p.Asp388Ala)
c.1088A>C (p.Asp363Ala)
c.1031A>C (p.Asp344Ala)
 dbSNP
3g.30672319A>GCA351808615TGFBR2c.1136A>G (p.Asp379Gly)
n.2732A>G
c.1211A>G (p.Asp404Gly)
c.1163A>G (p.Asp388Gly)
c.1088A>G (p.Asp363Gly)
c.1031A>G (p.Asp344Gly)
 dbSNP
3g.30672319A>TCA10587568TGFBR2c.1136A>T (p.Asp379Val)
n.2732A>T
c.1211A>T (p.Asp404Val)
c.1163A>T (p.Asp388Val)
c.1088A>T (p.Asp363Val)
c.1031A>T (p.Asp344Val)
 ClinVar dbSNP
3g.30672320C>ACA351808616TGFBR2c.1137C>A (p.Asp379Glu)
n.2733C>A
c.1212C>A (p.Asp404Glu)
c.1164C>A (p.Asp388Glu)
c.1089C>A (p.Asp363Glu)
c.1032C>A (p.Asp344Glu)
3g.30672320C=CA1354873240TGFBR2c.1137C= (p.Asp379=)
n.2733C=
c.1212C= (p.Asp404=)
c.1164C= (p.Asp388=)
c.1089C= (p.Asp363=)
c.1032C= (p.Asp344=)
3g.30672320C>GCA351808617TGFBR2c.1137C>G (p.Asp379Glu)
n.2733C>G
c.1212C>G (p.Asp404Glu)
c.1164C>G (p.Asp388Glu)
c.1089C>G (p.Asp363Glu)
c.1032C>G (p.Asp344Glu)
3g.30672320C>TCA432917598TGFBR2c.1137C>T (p.Asp379=)
n.2733C>T
c.1212C>T (p.Asp404=)
c.1164C>T (p.Asp388=)
c.1089C>T (p.Asp363=)
c.1032C>T (p.Asp344=)
 ClinVar dbSNP gnomAD v2 gnomAD v4
3g.30672321C>ACA351808618TGFBR2c.1138C>A (p.Leu380Ile)
n.2734C>A
c.1213C>A (p.Leu405Ile)
c.1165C>A (p.Leu389Ile)
c.1090C>A (p.Leu364Ile)
c.1033C>A (p.Leu345Ile)
 dbSNP
3g.30672321C>GCA351808619TGFBR2c.1138C>G (p.Leu380Val)
n.2734C>G
c.1213C>G (p.Leu405Val)
c.1165C>G (p.Leu389Val)
c.1090C>G (p.Leu364Val)
c.1033C>G (p.Leu345Val)
 dbSNP
3g.30672321C>TCA351808620TGFBR2c.1138C>T (p.Leu380Phe)
n.2734C>T
c.1213C>T (p.Leu405Phe)
c.1165C>T (p.Leu389Phe)
c.1090C>T (p.Leu364Phe)
c.1033C>T (p.Leu345Phe)
 dbSNP
3g.30672322T>ACA351808621TGFBR2c.1139T>A (p.Leu380His)
n.2735T>A
c.1214T>A (p.Leu405His)
c.1166T>A (p.Leu389His)
c.1091T>A (p.Leu364His)
c.1034T>A (p.Leu345His)
 dbSNP
3g.30672322T>CCA351808622TGFBR2c.1139T>C (p.Leu380Pro)
n.2735T>C
c.1214T>C (p.Leu405Pro)
c.1166T>C (p.Leu389Pro)
c.1091T>C (p.Leu364Pro)
c.1034T>C (p.Leu345Pro)
 dbSNP
3g.30672322T>GCA351808623TGFBR2c.1139T>G (p.Leu380Arg)
n.2735T>G
c.1214T>G (p.Leu405Arg)
c.1166T>G (p.Leu389Arg)
c.1091T>G (p.Leu364Arg)
c.1034T>G (p.Leu345Arg)
3g.30672323C>ACA432917599TGFBR2c.1140C>A (p.Leu380=)
n.2736C>A
c.1215C>A (p.Leu405=)
c.1167C>A (p.Leu389=)
c.1092C>A (p.Leu364=)
c.1035C>A (p.Leu345=)
 dbSNP
3g.30672323C=CA1354873241TGFBR2c.1140C= (p.Leu380=)
n.2736C=
c.1215C= (p.Leu405=)
c.1167C= (p.Leu389=)
c.1092C= (p.Leu364=)
c.1035C= (p.Leu345=)
3g.30672323C>GCA432917600TGFBR2c.1140C>G (p.Leu380=)
n.2736C>G
c.1215C>G (p.Leu405=)
c.1167C>G (p.Leu389=)
c.1092C>G (p.Leu364=)
c.1035C>G (p.Leu345=)
 dbSNP
3g.30672323C>TCA045767TGFBR2c.1140C>T (p.Leu380=)
n.2736C>T
c.1215C>T (p.Leu405=)
c.1167C>T (p.Leu389=)
c.1092C>T (p.Leu364=)
c.1035C>T (p.Leu345=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.30672324A>CCA351808624TGFBR2c.1141A>C (p.Lys381Gln)
n.2737A>C
c.1216A>C (p.Lys406Gln)
c.1168A>C (p.Lys390Gln)
c.1093A>C (p.Lys365Gln)
c.1036A>C (p.Lys346Gln)
3g.30672324A>GCA351808625TGFBR2c.1141A>G (p.Lys381Glu)
n.2737A>G
c.1216A>G (p.Lys406Glu)
c.1168A>G (p.Lys390Glu)
c.1093A>G (p.Lys365Glu)
c.1036A>G (p.Lys346Glu)
3g.30672324A>TCA351808626TGFBR2c.1141A>T (p.Lys381Ter)
n.2737A>T
c.1216A>T (p.Lys406Ter)
c.1168A>T (p.Lys390Ter)
c.1093A>T (p.Lys365Ter)
c.1036A>T (p.Lys346Ter)
 dbSNP
3g.30672325A=CA1354873242TGFBR2c.1142A= (p.Lys381=)
n.2738A=
c.1217A= (p.Lys406=)
c.1169A= (p.Lys390=)
c.1094A= (p.Lys365=)
c.1037A= (p.Lys346=)
3g.30672325A>CCA351808629TGFBR2c.1142A>C (p.Lys381Thr)
n.2738A>C
c.1217A>C (p.Lys406Thr)
c.1169A>C (p.Lys390Thr)
c.1094A>C (p.Lys365Thr)
c.1037A>C (p.Lys346Thr)
3g.30672325A>GCA351808627TGFBR2c.1142A>G (p.Lys381Arg)
n.2738A>G
c.1217A>G (p.Lys406Arg)
c.1169A>G (p.Lys390Arg)
c.1094A>G (p.Lys365Arg)
c.1037A>G (p.Lys346Arg)
 ClinVar dbSNP
3g.30672325A>TCA351808628TGFBR2c.1142A>T (p.Lys381Met)
n.2738A>T
c.1217A>T (p.Lys406Met)
c.1169A>T (p.Lys390Met)
c.1094A>T (p.Lys365Met)
c.1037A>T (p.Lys346Met)
 dbSNP
3g.30672326G>ACA432917601TGFBR2c.1143G>A (p.Lys381=)
n.2739G>A
c.1218G>A (p.Lys406=)
c.1170G>A (p.Lys390=)
c.1095G>A (p.Lys365=)
c.1038G>A (p.Lys346=)
 dbSNP
3g.30672326G>CCA351808630TGFBR2c.1143G>C (p.Lys381Asn)
n.2739G>C
c.1218G>C (p.Lys406Asn)
c.1170G>C (p.Lys390Asn)
c.1095G>C (p.Lys365Asn)
c.1038G>C (p.Lys346Asn)
 ClinVar dbSNP COSMIC COSMIC
3g.30672326G>TCA351808631TGFBR2c.1143G>T (p.Lys381Asn)
n.2739G>T
c.1218G>T (p.Lys406Asn)
c.1170G>T (p.Lys390Asn)
c.1095G>T (p.Lys365Asn)
c.1038G>T (p.Lys346Asn)

Number of alleles fetched