ClinVar Miner

List of variants in gene BRAT1 reported as benign for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_152743.4(BRAT1):c.128-10A>G rs2164688 0.46043
NM_152743.4(BRAT1):c.2388A>G (p.Glu796=) rs1043291 0.45840
NM_152743.4(BRAT1):c.924-149A>G rs3735104 0.45674
NM_152743.4(BRAT1):c.1932A>G (p.Arg644=) rs4719552 0.45541
NM_152743.4(BRAT1):c.1771-36C>A rs4721763 0.45462
NM_152743.4(BRAT1):c.1396-169G>C rs77056351 0.18535
NM_152743.4(BRAT1):c.-16-100G>A rs1866019 0.15447
NM_152743.4(BRAT1):c.699G>A (p.Thr233=) rs61753095 0.15251
NM_152743.4(BRAT1):c.1771-57C>T rs4721764 0.15244
NM_152743.4(BRAT1):c.430+20A>G rs34720091 0.12399
NM_152743.4(BRAT1):c.*12G>C rs1043294 0.12370
NM_152743.4(BRAT1):c.1931G>A (p.Arg644Gln) rs4719553 0.12363
NM_152743.4(BRAT1):c.803+59C>T rs13240450 0.12357
NM_152743.4(BRAT1):c.923+254C>T rs34108550 0.12345
NM_152743.4(BRAT1):c.1016-124C>T rs34947605 0.12344
NM_152743.4(BRAT1):c.1321+18G>A rs62442586 0.12338
NM_152743.4(BRAT1):c.-16-257G>A rs11773376 0.12318
NM_152743.4(BRAT1):c.128-38G>A rs6942871 0.09492
NM_152743.4(BRAT1):c.1923G>A (p.Ala641=) rs2917726 0.04425
NM_152743.4(BRAT1):c.1988G>A (p.Gly663Asp) rs61627394 0.04216
NM_152743.4(BRAT1):c.1798C>T (p.Leu600Phe) rs56727079 0.03653
NM_152743.4(BRAT1):c.1396-171T>C rs77045513 0.03625
NM_152743.4(BRAT1):c.128-220G>A rs6946899 0.03515
NM_152743.4(BRAT1):c.1395+44G>A rs115986733 0.02945
NM_152743.4(BRAT1):c.1598-56G>A rs75535462 0.02936
NM_152743.4(BRAT1):c.803+28G>A rs77887835 0.02821
NM_152743.4(BRAT1):c.2209C>T (p.Arg737Trp) rs60152725 0.02491
NM_152743.4(BRAT1):c.282+185G>A rs114060228 0.02349
NM_152743.4(BRAT1):c.1770+79G>A rs111436909 0.02167
NM_152743.4(BRAT1):c.854G>A (p.Arg285Gln) rs77213198 0.02022
NM_152743.4(BRAT1):c.924-14G>A rs113638677 0.02010
NM_152743.4(BRAT1):c.1636G>T (p.Val546Leu) rs34656552 0.01960
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320 0.01143
NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser) rs77015302 0.01031
NM_152743.4(BRAT1):c.924-13C>T rs73287544 0.00979
NM_152743.4(BRAT1):c.1135-8C>A rs113613637 0.00936
NM_152743.4(BRAT1):c.962T>G (p.Leu321Arg) rs150942467 0.00675
NM_152743.4(BRAT1):c.993G>A (p.Thr331=) rs76646873 0.00653
NM_152743.4(BRAT1):c.1884C>T (p.Ala628=) rs142346283 0.00625
NM_152743.4(BRAT1):c.866G>C (p.Cys289Ser) rs140451075 0.00598
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932 0.00249
NM_152743.4(BRAT1):c.1659C>T (p.Leu553=) rs61746940 0.00205
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616 0.00198
NM_152743.4(BRAT1):c.2208G>T (p.Leu736=) rs61753093 0.00159
NM_152743.4(BRAT1):c.1135-72G>A rs112257671
NM_152743.4(BRAT1):c.127+226G>A rs11974537
NM_152743.4(BRAT1):c.1396-235C>T rs77651117
NM_152743.4(BRAT1):c.2169T>A (p.Leu723=) rs150300694
NM_152743.4(BRAT1):c.282+304_282+305insTCTCTTCCTGGGATGGAGACAGGAGTCGTAGCTGCCCCATGGCCTCCG rs779685636
NM_152743.4(BRAT1):c.283-308del rs1185029266
NM_152743.4(BRAT1):c.431-102dup rs147960160
NM_152743.4(BRAT1):c.431-88_431-61del rs11267702

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.