ClinVar Miner

List of variants in gene BRAT1 reported as likely pathogenic by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152743.4(BRAT1):c.283-2A>T rs147005619 0.00006
NM_152743.4(BRAT1):c.1016-1G>C
NM_152743.4(BRAT1):c.1135-1G>T
NM_152743.4(BRAT1):c.1322-2A>G rs2128390167
NM_152743.4(BRAT1):c.1371_1395+16del rs1224820591
NM_152743.4(BRAT1):c.1395+2T>A rs1779105755
NM_152743.4(BRAT1):c.1499-1G>T rs1778987915
NM_152743.4(BRAT1):c.1598-1G>A
NM_152743.4(BRAT1):c.1710del (p.Gln571fs) rs756489141
NM_152743.4(BRAT1):c.283-1G>A
NM_152743.4(BRAT1):c.283-2A>G
NM_152743.4(BRAT1):c.804-1G>T
NM_152743.4(BRAT1):c.924-1G>A

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.