ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported by PreventionGenetics, part of Exact Sciences

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Total variants: 53
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.234C>T (p.Ser78=) rs9901455 0.15951
NM_002878.4(RAD51D):c.494G>A (p.Arg165Gln) rs4796033 0.11973
NM_002878.4(RAD51D):c.698A>G (p.Glu233Gly) rs28363284 0.01102
NM_002878.4(RAD51D):c.695G>A (p.Arg232Gln) rs28363283 0.00457
NM_002878.4(RAD51D):c.873C>T (p.Arg291=) rs140848654 0.00399
NM_002878.4(RAD51D):c.666A>G (p.Glu222=) rs114012742 0.00131
NM_002878.4(RAD51D):c.263+1588A>G rs180869630 0.00123
NM_002878.4(RAD51D):c.146C>T (p.Ala49Val) rs140317560 0.00116
NM_002878.4(RAD51D):c.263+1509C>T rs201506572 0.00116
NM_002878.4(RAD51D):c.919G>A (p.Glu307Lys) rs115031549 0.00083
NM_002878.4(RAD51D):c.263+1570T>A rs376472075 0.00078
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.263+1605G>A rs147933658 0.00023
NM_002878.4(RAD51D):c.434G>A (p.Arg145His) rs147264215 0.00023
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile) rs138969595 0.00021
NM_002878.4(RAD51D):c.39C>G (p.Thr13=) rs146448657 0.00018
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
NM_002878.4(RAD51D):c.263+1474C>T rs201720876 0.00016
NM_002878.4(RAD51D):c.196G>A (p.Val66Met) rs56026142 0.00009
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.145-4G>A rs201361465 0.00006
NM_002878.4(RAD51D):c.307A>G (p.Thr103Ala) rs781378161 0.00005
NM_002878.4(RAD51D):c.346-10C>T rs779972784 0.00005
NM_002878.4(RAD51D):c.667+20C>T rs373473666 0.00004
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.481-8C>T rs762247126 0.00003
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter) rs387906843 0.00003
NM_002878.4(RAD51D):c.765G>A (p.Arg255=) rs751833940 0.00003
NM_002878.4(RAD51D):c.878C>T (p.Ala293Val) rs769732230 0.00003
NM_002878.4(RAD51D):c.263+1612del rs750282687 0.00002
NM_002878.4(RAD51D):c.108G>A (p.Leu36=) rs755962971 0.00001
NM_002878.4(RAD51D):c.12C>G (p.Leu4=) rs786203193 0.00001
NM_002878.4(RAD51D):c.576+19C>T rs749835057 0.00001
NM_002878.4(RAD51D):c.607G>A (p.Val203Met) rs730881947 0.00001
NM_002878.4(RAD51D):c.621G>T (p.Ser207=) rs749859221 0.00001
NM_002878.4(RAD51D):c.758G>A (p.Arg253Gln) rs1060502963 0.00001
NM_002878.4(RAD51D):c.900A>G (p.Arg300=) rs370634278 0.00001
NM_002878.4(RAD51D):c.-7G>A rs553444507
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+1475G>A
NM_002878.4(RAD51D):c.263+1558A>G
NM_002878.4(RAD51D):c.263+1628G>A
NM_002878.4(RAD51D):c.263+1G>A rs1555570242
NM_002878.4(RAD51D):c.340dup (p.Thr114fs)
NM_002878.4(RAD51D):c.342T>C (p.Thr114=)
NM_002878.4(RAD51D):c.348A>T (p.Val116=) rs1233886388
NM_002878.4(RAD51D):c.598G>A (p.Val200Met) rs1567726600
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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