ClinVar Miner

List of variants in gene BRAT1 reported as benign by GeneDx

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Gene type:
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Total variants: 48
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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.1932A>G (p.Arg644=) rs4719552 0.45541
NM_152743.4(BRAT1):c.924-149A>G rs3735104 0.44812
NM_152743.4(BRAT1):c.1771-36C>A rs4721763 0.44596
NM_152743.4(BRAT1):c.1396-169G>C rs77056351 0.18535
NM_152743.4(BRAT1):c.699G>A (p.Thr233=) rs61753095 0.15210
NM_152743.4(BRAT1):c.1771-57C>T rs4721764 0.15200
NM_152743.4(BRAT1):c.-16-100G>A rs1866019 0.14909
NM_152743.4(BRAT1):c.1396-235C>T rs77651117 0.12532
NM_152743.4(BRAT1):c.*12G>C rs1043294 0.12370
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.430+20A>G rs34720091 0.12208
NM_152743.4(BRAT1):c.1931G>A (p.Arg644Gln) rs4719553 0.12177
NM_152743.4(BRAT1):c.803+59C>T rs13240450 0.12169
NM_152743.4(BRAT1):c.1321+18G>A rs62442586 0.12144
NM_152743.4(BRAT1):c.-16-257G>A rs11773376 0.12123
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 0.04139
NM_152743.4(BRAT1):c.1396-171T>C rs77045513 0.03625
NM_152743.4(BRAT1):c.128-220G>A rs6946899 0.03259
NM_152743.4(BRAT1):c.803+28G>A rs77887835 0.02975
NM_152743.4(BRAT1):c.1395+44G>A rs115986733 0.02945
NM_152743.4(BRAT1):c.1598-56G>A rs75535462 0.02708
NM_152743.4(BRAT1):c.854G>A (p.Arg285Gln) rs77213198 0.02626
NM_152743.4(BRAT1):c.2209C>T (p.Arg737Trp) rs60152725 0.02491
NM_152743.4(BRAT1):c.282+185G>A rs114060228 0.02170
NM_152743.4(BRAT1):c.1770+79G>A rs111436909 0.02017
NM_152743.4(BRAT1):c.1636G>T (p.Val546Leu) rs34656552 0.01960
NM_152743.4(BRAT1):c.924-14G>A rs113638677 0.01870
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320 0.01143
NM_152743.4(BRAT1):c.924-13C>T rs73287544 0.00979
NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser) rs77015302 0.00966
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.866G>C (p.Cys289Ser) rs140451075 0.00577
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932 0.00248
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616 0.00198
NM_152743.4(BRAT1):c.1135-72G>A rs112257671
NM_152743.4(BRAT1):c.127+226G>A rs11974537
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

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