ClinVar Miner

List of variants in gene BRAT1 reported as benign for not provided

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Gene type:
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Total variants: 17
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HGVS dbSNP
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.1701C>T (p.Thr567=) rs199766692
NM_152743.4(BRAT1):c.1726G>A (p.Gly576Ser) rs61740320
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.1884C>T (p.Ala628=) rs142346283
NM_152743.4(BRAT1):c.1923G>A (p.Ala641=) rs2917726
NM_152743.4(BRAT1):c.1932A>G (p.Arg644=) rs4719552
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.2353C>T (p.Arg785Trp) rs61729932
NM_152743.4(BRAT1):c.2388A>G (p.Glu796=) rs1043291
NM_152743.4(BRAT1):c.699G>A (p.Thr233=) rs61753095
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.993G>A (p.Thr331=) rs76646873

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