ClinVar Miner

List of variants in gene BRAT1 reported as uncertain significance for not provided

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Total variants: 27
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HGVS dbSNP
NM_152743.4(BRAT1):c.1087G>A (p.Gly363Ser) rs967919052
NM_152743.4(BRAT1):c.1267G>A (p.Val423Ile) rs141807337
NM_152743.4(BRAT1):c.1280G>A (p.Arg427Gln) rs375466838
NM_152743.4(BRAT1):c.1340C>T (p.Thr447Met) rs368808380
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.1522C>T (p.Arg508Cys) rs751548415
NM_152743.4(BRAT1):c.158C>G (p.Pro53Arg) rs368397368
NM_152743.4(BRAT1):c.1702G>A (p.Ala568Thr) rs141709461
NM_152743.4(BRAT1):c.1792C>T (p.His598Tyr) rs201523118
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp) rs61753094
NM_152743.4(BRAT1):c.1879G>A (p.Ala627Thr) rs750400556
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.2329A>G (p.Arg777Gly) rs773571503
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932
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.491C>T (p.Ala164Val) rs771600489
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.652C>G (p.Leu218Val) rs1471856951
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.853C>T (p.Arg285Trp) rs1301692811
NM_152743.4(BRAT1):c.983T>C (p.Leu328Pro) rs1291695271

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