ClinVar Miner

List of variants in gene TGFBR2 reported as likely benign by Color

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 18
Download table as spreadsheet
NM_001024847.2(TGFBR2):c.118G>A (p.Asp40Asn) rs61732532
NM_001024847.2(TGFBR2):c.129C>T (p.Ile43=) rs143701368
NM_003242.6(TGFBR2):c.1116G>A (p.Lys372=) rs753782498
NM_003242.6(TGFBR2):c.1119G>A (p.Met373Ile) rs35719192
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.1208G>A (p.Arg403His) rs143095746
NM_003242.6(TGFBR2):c.1255-15C>G rs563937625
NM_003242.6(TGFBR2):c.1335C>T (p.Thr445=) rs546058122
NM_003242.6(TGFBR2):c.1525-7G>A rs377499122
NM_003242.6(TGFBR2):c.1626G>A (p.Glu542=) rs375226321
NM_003242.6(TGFBR2):c.207C>T (p.Ser69=) rs1559456575
NM_003242.6(TGFBR2):c.455-5A>G rs747104789
NM_003242.6(TGFBR2):c.528G>A (p.Leu176=) rs1303407125
NM_003242.6(TGFBR2):c.708C>T (p.Asn236=) rs141554621
NM_003242.6(TGFBR2):c.95-7T>C rs764533083
NM_003242.6(TGFBR2):c.984C>T (p.His328=) rs193922666
NM_003242.6(TGFBR2):c.9G>A (p.Arg3=) rs1559443648

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.