ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as pathogenic for Hereditary cancer-predisposing syndrome

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Total variants: 35
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HGVS dbSNP
NM_002878.3(RAD51D):c.140_141insAA (p.Tyr47Terfs) rs587782736
NM_002878.3(RAD51D):c.178C>T (p.Gln60Ter) rs1555570285
NM_002878.3(RAD51D):c.185_200del16 (p.Ser62Leufs) rs786202179
NM_002878.3(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.3(RAD51D):c.210_229dup (p.Thr77Ilefs) rs1555570266
NM_002878.3(RAD51D):c.216C>A (p.Tyr72Ter) rs148690585
NM_002878.3(RAD51D):c.270_271dupTA (p.Lys91Ilefs) rs753862052
NM_002878.3(RAD51D):c.270_271insTA (p.Lys91Terfs) rs730881943
NM_002878.3(RAD51D):c.2dup (p.Met1Ilefs) rs772306012
NM_002878.3(RAD51D):c.326dupC (p.Gly110Argfs) rs730882119
NM_002878.3(RAD51D):c.330dupT (p.Ser111Terfs) rs786202434
NM_002878.3(RAD51D):c.343C>T (p.Gln115Ter) rs1555568473
NM_002878.3(RAD51D):c.357_360delTATG (p.Cys119Trpfs) rs876658297
NM_002878.3(RAD51D):c.363delA (p.Ala122Glnfs) rs730881935
NM_002878.3(RAD51D):c.442C>T (p.Gln148Ter) rs773906955
NM_002878.3(RAD51D):c.451C>T (p.Gln151Ter) rs587781756
NM_002878.3(RAD51D):c.463C>T (p.Gln155Ter) rs1555568293
NM_002878.3(RAD51D):c.478C>T (p.Gln160Ter) rs1057521922
NM_002878.3(RAD51D):c.547C>T (p.Gln183Ter) rs587782695
NM_002878.3(RAD51D):c.556C>T (p.Arg186Ter) rs387906843
NM_002878.3(RAD51D):c.564delT (p.Val189Trpfs) rs786202750
NM_002878.3(RAD51D):c.623dup (p.Thr209Hisfs) rs1555567610
NM_002878.3(RAD51D):c.649G>T (p.Gly217Ter) rs775365939
NM_002878.3(RAD51D):c.649_655delGGAGGTCinsTGAGGTT (p.Gly217Ter) rs587781527
NM_002878.3(RAD51D):c.655C>T (p.Gln219Ter) rs771007945
NM_002878.3(RAD51D):c.664delG (p.Glu222Lysfs) rs1555567586
NM_002878.3(RAD51D):c.671T>A (p.Leu224Ter)
NM_002878.3(RAD51D):c.694C>T (p.Arg232Ter) rs587780104
NM_002878.3(RAD51D):c.748delC (p.His250Thrfs) rs587780105
NM_002878.3(RAD51D):c.757C>T (p.Arg253Ter) rs137886232
NM_002878.3(RAD51D):c.803G>A (p.Trp268Ter) rs750219200
NM_002878.3(RAD51D):c.81delA (p.Val28Trpfs) rs1064793952
NM_002878.3(RAD51D):c.94_95delGT (p.Val32Phefs) rs786203137
NM_002878.3:c.254delG
NM_002878.3:c.508del

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