ClinVar Miner

List of variants in gene BRAT1 reported as benign by Athena Diagnostics Inc

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Gene type:
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Total variants: 20
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HGVS dbSNP gnomAD frequency
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.699G>A (p.Thr233=) rs61753095 0.15251
NM_152743.4(BRAT1):c.1923G>A (p.Ala641=) rs2917726 0.04425
NM_152743.4(BRAT1):c.1798C>T (p.Leu600Phe) rs56727079 0.03653
NM_152743.4(BRAT1):c.2209C>T (p.Arg737Trp) rs60152725 0.02491
NM_152743.4(BRAT1):c.854G>A (p.Arg285Gln) rs77213198 0.02022
NM_152743.4(BRAT1):c.1636G>T (p.Val546Leu) rs34656552 0.01960
NM_152743.4(BRAT1):c.1206C>T (p.Asp402=) rs7807895 0.01413
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320 0.01143
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.1579C>T (p.Leu527=) rs151161353 0.00126
NM_152743.4(BRAT1):c.1931_1932delinsAG (p.Arg644Gln) rs71531463
NM_152743.4(BRAT1):c.2169T>A (p.Leu723=) rs150300694

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