ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as likely benign for not provided

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Total variants: 20
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HGVS dbSNP
NM_002878.3(RAD51D):c.12C>G (p.Leu4=) rs786203193
NM_002878.3(RAD51D):c.145-4G>A rs201361465
NM_002878.3(RAD51D):c.146C>T (p.Ala49Val) rs140317560
NM_002878.3(RAD51D):c.223C>T (p.Leu75=) rs746929682
NM_002878.3(RAD51D):c.263+1323C>A
NM_002878.3(RAD51D):c.263+1816C>T
NM_002878.3(RAD51D):c.263+1855G>A
NM_002878.3(RAD51D):c.263+1857_263+1858insT
NM_002878.3(RAD51D):c.263+7G>A rs56218020
NM_002878.3(RAD51D):c.26G>C (p.Cys9Ser) rs140825795
NM_002878.3(RAD51D):c.39C>G (p.Thr13=) rs146448657
NM_002878.3(RAD51D):c.576+19C>T rs749835057
NM_002878.3(RAD51D):c.577-211T>C
NM_002878.3(RAD51D):c.667+20C>T rs373473666
NM_002878.3(RAD51D):c.66C>T (p.Ser22=) rs876660902
NM_002878.3(RAD51D):c.82+128C>T
NM_002878.3(RAD51D):c.82+5_82+12del
NM_002878.3(RAD51D):c.879G>C (p.Ala293=) rs368209468
NM_002878.3(RAD51D):c.903+53C>T
NM_002878.3(RAD51D):c.904-3C>T rs45478491

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