ClinVar Miner

List of variants in gene BRAT1 reported by Athena Diagnostics Inc

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Gene type:
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Total variants: 39
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HGVS dbSNP
NM_152743.4(BRAT1):c.1032G>A (p.Thr344=) rs371220513
NM_152743.4(BRAT1):c.1087G>A (p.Gly363Ser) rs967919052
NM_152743.4(BRAT1):c.1206C>T (p.Asp402=) rs7807895
NM_152743.4(BRAT1):c.1267G>A (p.Val423Ile) rs141807337
NM_152743.4(BRAT1):c.1451C>G (p.Thr484Ser) rs200248064
NM_152743.4(BRAT1):c.1484C>T (p.Pro495Leu) rs577945739
NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser) rs147745609
NM_152743.4(BRAT1):c.1579C>T (p.Leu527=) rs151161353
NM_152743.4(BRAT1):c.1636G>T (p.Val546Leu) rs34656552
NM_152743.4(BRAT1):c.1659C>T (p.Leu553=) rs61746940
NM_152743.4(BRAT1):c.1702G>A (p.Ala568Thr) rs141709461
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320
NM_152743.4(BRAT1):c.1792C>T (p.His598Tyr) rs201523118
NM_152743.4(BRAT1):c.1798C>T (p.Leu600Phe) rs56727079
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp) rs61753094
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616
NM_152743.4(BRAT1):c.1884C>T (p.Ala628=) rs142346283
NM_152743.4(BRAT1):c.1923G>A (p.Ala641=) rs2917726
NM_152743.4(BRAT1):c.1931_1932delinsAG (p.Arg644Gln) rs71531463
NM_152743.4(BRAT1):c.1932A>G (p.Arg644=) rs4719552
NM_152743.4(BRAT1):c.2029G>A (p.Val677Met) rs141726264
NM_152743.4(BRAT1):c.2041G>A (p.Glu681Lys) rs145833100
NM_152743.4(BRAT1):c.2169T>A (p.Leu723=) rs150300694
NM_152743.4(BRAT1):c.2208G>T (p.Leu736=) rs61753093
NM_152743.4(BRAT1):c.2209C>T (p.Arg737Trp) rs60152725
NM_152743.4(BRAT1):c.2329A>G (p.Arg777Gly) rs773571503
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932
NM_152743.4(BRAT1):c.2388A>G (p.Glu796=) rs1043291
NM_152743.4(BRAT1):c.346G>A (p.Val116Ile) rs750543404
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val) rs140833277
NM_152743.4(BRAT1):c.578C>T (p.Ala193Val) rs144841598
NM_152743.4(BRAT1):c.626C>T (p.Ala209Val) rs112960104
NM_152743.4(BRAT1):c.699G>A (p.Thr233=) rs61753095
NM_152743.4(BRAT1):c.811G>A (p.Val271Met) rs746527927
NM_152743.4(BRAT1):c.814T>C (p.Phe272Leu) rs1562577958
NM_152743.4(BRAT1):c.854G>A (p.Arg285Gln) rs77213198
NM_152743.4(BRAT1):c.866G>C (p.Cys289Ser) rs140451075
NM_152743.4(BRAT1):c.962T>G (p.Leu321Arg) rs150942467
NM_152743.4(BRAT1):c.993G>A (p.Thr331=) rs76646873

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