ClinVar Miner

List of variants in gene TGFBR2 reported as likely benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_001024847.2(TGFBR2):c.111C>T (p.Ala37=) rs149757320
NM_001024847.2(TGFBR2):c.118G>A (p.Asp40Asn) rs61732532
NM_001024847.2(TGFBR2):c.136A>C (p.Ser46Arg) rs200111443
NM_003242.5(TGFBR2):c.1525-11delT rs1064795299
NM_003242.5(TGFBR2):c.454+17_454+47del31ins22
NM_003242.6(TGFBR2):c.*11G>A rs886038529
NM_003242.6(TGFBR2):c.-31G>A rs767154664
NM_003242.6(TGFBR2):c.1014G>A (p.Thr338=) rs764720370
NM_003242.6(TGFBR2):c.1015C>T (p.Arg339Trp) rs761991787
NM_003242.6(TGFBR2):c.1062C>T (p.Leu354=) rs113194608
NM_003242.6(TGFBR2):c.1092T>C (p.Asp364=) rs149195553
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192
NM_003242.6(TGFBR2):c.1128G>A (p.Val376=) rs1057523953
NM_003242.6(TGFBR2):c.1158C>T (p.Leu386=) rs757158964
NM_003242.6(TGFBR2):c.1159G>A (p.Val387Met) rs35766612
NM_003242.6(TGFBR2):c.1159G>T (p.Val387Leu) rs35766612
NM_003242.6(TGFBR2):c.115A>T (p.Thr39Ser) rs780280433
NM_003242.6(TGFBR2):c.1185G>C (p.Leu395=) rs193922663
NM_003242.6(TGFBR2):c.1208G>A (p.Arg403His) rs143095746
NM_003242.6(TGFBR2):c.1254+12C>T rs763098114
NM_003242.6(TGFBR2):c.1254+8A>G rs200630803
NM_003242.6(TGFBR2):c.1452C>T (p.Val484=) rs185502982
NM_003242.6(TGFBR2):c.1464G>A (p.Lys488=) rs753282415
NM_003242.6(TGFBR2):c.1525-5T>C rs770896804
NM_003242.6(TGFBR2):c.1525-6C>G rs748388518
NM_003242.6(TGFBR2):c.1548G>A (p.Thr516=) rs140662877
NM_003242.6(TGFBR2):c.1569C>T (p.His523=) rs760107571
NM_003242.6(TGFBR2):c.1602G>A (p.Val534=) rs140818646
NM_003242.6(TGFBR2):c.263+17A>C rs34771516
NM_003242.6(TGFBR2):c.263+7_263+9delinsGAC rs1064794518
NM_003242.6(TGFBR2):c.297A>G (p.Thr99=) rs727504343
NM_003242.6(TGFBR2):c.437A>G (p.Asn146Ser) rs863223836
NM_003242.6(TGFBR2):c.455-4T>C rs11466512
NM_003242.6(TGFBR2):c.617C>T (p.Thr206Met) rs150022335
NM_003242.6(TGFBR2):c.639C>T (p.Ser213=) rs200332401
NM_003242.6(TGFBR2):c.690G>A (p.Thr230=) rs201560560
NM_003242.6(TGFBR2):c.81C>T (p.His27=) rs1057520957
NM_003242.6(TGFBR2):c.933G>A (p.Glu311=) rs754003334
NM_003242.6(TGFBR2):c.94+16202A>G rs375610471
NM_003242.6(TGFBR2):c.94+16308T>C rs770994456
NM_003242.6(TGFBR2):c.944C>T (p.Thr315Met) rs34833812
NM_003242.6(TGFBR2):c.95-20A>G rs371326218

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.