ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported as uncertain significance by Preventiongenetics, part of Exact Sciences

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Total variants: 15
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.864C>T (p.Gly288=) rs138557828 0.00009
NM_002878.4(RAD51D):c.973G>A (p.Gly325Ser) rs587780106 0.00008
NM_002878.4(RAD51D):c.793G>A (p.Gly265Arg) rs140285068 0.00004
NM_002878.4(RAD51D):c.796C>T (p.Arg266Cys) rs587781813 0.00004
NM_002878.4(RAD51D):c.263+1612del rs750282687 0.00002
NM_002878.4(RAD51D):c.607G>A (p.Val203Met) rs730881947 0.00001
NM_002878.4(RAD51D):c.758G>A (p.Arg253Gln) rs1060502963 0.00001
NM_002878.4(RAD51D):c.136T>C (p.Ser46Pro) rs980673532
NM_002878.4(RAD51D):c.190T>C (p.Phe64Leu) rs371182137
NM_002878.4(RAD51D):c.263+1558A>G
NM_002878.4(RAD51D):c.263+1G>A rs1555570242
NM_002878.4(RAD51D):c.680T>C (p.Met227Thr) rs773485482
NM_002878.4(RAD51D):c.833T>C (p.Leu278Pro) rs1567724873
NM_002878.4(RAD51D):c.979C>T (p.Gln327Ter) rs786203974

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