ClinVar Miner

List of variants in gene BRWD3 reported as likely benign by Ambry Genetics

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Gene type:
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Total variants: 25
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HGVS dbSNP gnomAD frequency
NM_153252.5(BRWD3):c.33G>A (p.Glu11=) rs139071237 0.00422
NM_153252.5(BRWD3):c.2346T>C (p.Cys782=) rs183513696 0.00033
NM_153252.5(BRWD3):c.2184G>A (p.Ala728=) rs369118921 0.00026
NM_153252.5(BRWD3):c.3318A>G (p.Pro1106=) rs140203774 0.00011
NM_153252.5(BRWD3):c.4088A>G (p.Gln1363Arg) rs143824970 0.00004
NM_153252.5(BRWD3):c.1962G>A (p.Leu654=) rs1234088480 0.00001
NM_153252.5(BRWD3):c.1227G>A (p.Met409Ile)
NM_153252.5(BRWD3):c.1233C>T (p.Gly411=)
NM_153252.5(BRWD3):c.1490G>A (p.Arg497Gln)
NM_153252.5(BRWD3):c.1506G>T (p.Arg502=)
NM_153252.5(BRWD3):c.1761A>G (p.Pro587=) rs1569261058
NM_153252.5(BRWD3):c.225T>C (p.Ile75=)
NM_153252.5(BRWD3):c.2502C>T (p.Asp834=)
NM_153252.5(BRWD3):c.2542A>G (p.Ser848Gly)
NM_153252.5(BRWD3):c.309G>C (p.Gln103His)
NM_153252.5(BRWD3):c.3578G>A (p.Arg1193Gln)
NM_153252.5(BRWD3):c.381A>G (p.Arg127=) rs1569289747
NM_153252.5(BRWD3):c.3837C>T (p.Asp1279=)
NM_153252.5(BRWD3):c.3875G>A (p.Arg1292Gln)
NM_153252.5(BRWD3):c.3936A>G (p.Leu1312=)
NM_153252.5(BRWD3):c.4234A>C (p.Ile1412Leu)
NM_153252.5(BRWD3):c.4546G>C (p.Asp1516His)
NM_153252.5(BRWD3):c.4573G>A (p.Gly1525Ser)
NM_153252.5(BRWD3):c.4651C>G (p.Gln1551Glu)
NM_153252.5(BRWD3):c.4872C>T (p.Asp1624=)

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