ClinVar Miner

List of variants in gene BCOR reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 31
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001123385.2(BCOR):c.2424T>C (p.Leu808=) rs142968718 0.00085
NM_001123385.2(BCOR):c.2423T>A (p.Leu808His) rs151125150 0.00083
NM_001123385.2(BCOR):c.3533G>A (p.Ser1178Asn) rs375639152 0.00076
NM_001123385.2(BCOR):c.4488A>C (p.Ala1496=) rs138741225 0.00076
NM_001123385.2(BCOR):c.3802A>G (p.Arg1268Gly) rs140897453 0.00058
NM_001123385.2(BCOR):c.2035G>A (p.Val679Ile) rs144722432 0.00053
NM_001123385.2(BCOR):c.4724T>C (p.Met1575Thr) rs142595337 0.00043
NM_001123385.2(BCOR):c.3378C>T (p.His1126=) rs137923016 0.00030
NM_001123385.2(BCOR):c.5001G>A (p.Ser1667=) rs375878497 0.00012
NM_001123385.2(BCOR):c.4320T>C (p.Pro1440=) rs753786462 0.00011
NM_001123385.2(BCOR):c.3491G>A (p.Arg1164Gln) rs769057299 0.00006
NM_001123385.2(BCOR):c.4890C>T (p.Asp1630=) rs750330961 0.00006
NM_001123385.2(BCOR):c.1620G>A (p.Arg540=) rs144347073 0.00005
NM_001123385.2(BCOR):c.4152C>T (p.Tyr1384=) rs750973796 0.00005
NM_001123385.2(BCOR):c.179C>T (p.Thr60Met) rs202121665 0.00004
NM_001123385.2(BCOR):c.1651G>A (p.Asp551Asn) rs372463512 0.00003
NM_001123385.2(BCOR):c.2512C>T (p.Pro838Ser) rs148571491 0.00003
NM_001123385.2(BCOR):c.4053C>T (p.Thr1351=) rs781252900 0.00003
NM_001123385.2(BCOR):c.1707C>T (p.Ser569=) rs1438078198 0.00001
NM_001123385.2(BCOR):c.1779C>T (p.Ser593=)
NM_001123385.2(BCOR):c.2288G>T (p.Arg763Leu) rs139011455
NM_001123385.2(BCOR):c.3120C>T (p.Asp1040=)
NM_001123385.2(BCOR):c.3305T>C (p.Val1102Ala) rs111622737
NM_001123385.2(BCOR):c.3305T>G (p.Val1102Gly) rs111622737
NM_001123385.2(BCOR):c.3348C>T (p.Pro1116=)
NM_001123385.2(BCOR):c.3801C>G (p.Asn1267Lys)
NM_001123385.2(BCOR):c.3893C>T (p.Ser1298Phe)
NM_001123385.2(BCOR):c.4281A>T (p.Pro1427=)
NM_001123385.2(BCOR):c.4891G>A (p.Asp1631Asn)
NM_001123385.2(BCOR):c.4908G>A (p.Val1636=)
NM_001123385.2(BCOR):c.86+6T>C

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.