ClinVar Miner

List of variants in gene BRAT1 reported as benign

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP
NM_152743.4(BRAT1):c.1134+14G>A
NM_152743.4(BRAT1):c.1135-8C>A rs113613637
NM_152743.4(BRAT1):c.1196G>A (p.Arg399Gln) rs371360176
NM_152743.4(BRAT1):c.1206C>T (p.Asp402=) rs7807895
NM_152743.4(BRAT1):c.128-10A>G
NM_152743.4(BRAT1):c.1305G>T (p.Thr435=) rs145506790
NM_152743.4(BRAT1):c.1321+18G>A
NM_152743.4(BRAT1):c.1499-8C>T rs370879134
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.166G>A (p.Val56Met) rs148548421
NM_152743.4(BRAT1):c.1689G>A (p.Ala563=) rs146276208
NM_152743.4(BRAT1):c.1701C>T (p.Thr567=) rs199766692
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320
NM_152743.4(BRAT1):c.1740C>T (p.Pro580=) rs200084998
NM_152743.4(BRAT1):c.1798C>T (p.Leu600Phe) rs56727079
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616
NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser) rs77015302
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.1931G>A (p.Arg644Gln)
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.1988G>A (p.Gly663Asp)
NM_152743.4(BRAT1):c.2052A>G (p.Pro684=) rs775271322
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.2250C>T (p.Ala750=) rs543555790
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.282+9G>A rs192133446
NM_152743.4(BRAT1):c.430+20A>G
NM_152743.4(BRAT1):c.431G>A (p.Gly144Asp) rs199745325
NM_152743.4(BRAT1):c.560C>G (p.Pro187Arg)
NM_152743.4(BRAT1):c.566G>T (p.Gly189Val) rs531827528
NM_152743.4(BRAT1):c.675C>T (p.Phe225=) rs139443843
NM_152743.4(BRAT1):c.699G>A (p.Thr233=) rs61753095
NM_152743.4(BRAT1):c.762C>T (p.Pro254=) rs143192367
NM_152743.4(BRAT1):c.825C>T (p.Ser275=) rs141320181
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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