ClinVar Miner

List of variants in gene BRCA2 reported by Cancer Molecular Diagnostics Core, Tianjin Medical University Cancer Institute and Hospital

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000059.4(BRCA2):c.112G>A (p.Glu38Lys) rs1555280344
NM_000059.4(BRCA2):c.266C>A (p.Pro89Gln) rs748609599
NM_000059.4(BRCA2):c.2719A>G (p.Lys907Glu) rs876659600
NM_000059.4(BRCA2):c.3883C>T (p.Gln1295Ter) rs879255309
NM_000059.4(BRCA2):c.4025G>A (p.Ser1342Asn) rs1270552356
NM_000059.4(BRCA2):c.6149dup (p.Asn2051fs) rs1555284566
NM_000059.4(BRCA2):c.8165C>T (p.Thr2722Ile) rs80359062
NM_000059.4(BRCA2):c.8465_8472del (p.Ile2822fs) rs1555287661
NM_000059.4(BRCA2):c.8477A>T (p.Tyr2826Phe) rs1555287666
NM_000059.4(BRCA2):c.8713dup (p.Tyr2905fs) rs1555288169

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.