ClinVar Miner

List of variants in gene combination RAD51D, RAD51L3-RFFL reported by Counsyl

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 71
Download table as spreadsheet
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.771C>T (p.Ser257=) rs146212490 0.00206
NM_002878.4(RAD51D):c.-99T>C rs533209845 0.00193
NM_002878.4(RAD51D):c.481-7G>A rs145832514 0.00171
NM_002878.4(RAD51D):c.568G>A (p.Ala190Thr) rs80116829 0.00167
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.263+1570T>A rs376472075 0.00078
NM_002878.4(RAD51D):c.932T>A (p.Ile311Asn) rs145309168 0.00041
NM_002878.4(RAD51D):c.904-11T>A rs374449943 0.00038
NM_002878.4(RAD51D):c.26G>C (p.Cys9Ser) rs140825795 0.00037
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
NM_002878.4(RAD51D):c.413A>G (p.Asn138Ser) rs201676898 0.00025
NM_002878.4(RAD51D):c.263+1605G>A rs147933658 0.00023
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile) rs138969595 0.00021
NM_002878.4(RAD51D):c.264-14del rs757481281 0.00019
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
NM_002878.4(RAD51D):c.137C>G (p.Ser46Cys) rs587780102 0.00010
NM_002878.4(RAD51D):c.196G>A (p.Val66Met) rs56026142 0.00009
NM_002878.4(RAD51D):c.263+1627C>T rs188981311 0.00008
NM_002878.4(RAD51D):c.394G>A (p.Val132Ile) rs201141245 0.00007
NM_002878.4(RAD51D):c.145-4G>A rs201361465 0.00006
NM_002878.4(RAD51D):c.263+7G>A rs56218020 0.00006
NM_002878.4(RAD51D):c.629C>T (p.Ala210Val) rs376855484 0.00006
NM_002878.4(RAD51D):c.715C>T (p.Arg239Trp) rs770250516 0.00006
NM_002878.4(RAD51D):c.145-13G>T rs760867838 0.00004
NM_002878.4(RAD51D):c.145-14G>C rs200470533 0.00004
NM_002878.4(RAD51D):c.694C>T (p.Arg232Ter) rs587780104 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.53A>G (p.Gln18Arg) rs546225564 0.00003
NM_002878.4(RAD51D):c.556C>T (p.Arg186Ter) rs387906843 0.00003
NM_002878.4(RAD51D):c.263+1612del rs750282687 0.00002
NM_002878.4(RAD51D):c.363del (p.Ala122fs) rs730881935 0.00002
NM_002878.4(RAD51D):c.451C>T (p.Gln151Ter) rs587781756 0.00002
NM_002878.4(RAD51D):c.576+1G>A rs781161543 0.00002
NM_002878.4(RAD51D):c.620C>T (p.Ser207Leu) rs370228071 0.00002
NM_002878.4(RAD51D):c.131G>A (p.Gly44Asp) rs374730714 0.00001
NM_002878.4(RAD51D):c.198G>T (p.Val66=) rs200810304 0.00001
NM_002878.4(RAD51D):c.286G>T (p.Gly96Cys) rs762951311 0.00001
NM_002878.4(RAD51D):c.433C>T (p.Arg145Cys) rs755173206 0.00001
NM_002878.4(RAD51D):c.649G>T (p.Gly217Ter) rs775365939 0.00001
NM_002878.4(RAD51D):c.655C>T (p.Gln219Ter) rs771007945 0.00001
NM_002878.4(RAD51D):c.716G>A (p.Arg239Gln) rs780921112 0.00001
NM_002878.4(RAD51D):c.739-10T>C rs199998187 0.00001
NM_002878.4(RAD51D):c.739-3C>T rs1235042092 0.00001
NM_002878.4(RAD51D):c.1A>G (p.Met1Val) rs561425038
NM_002878.4(RAD51D):c.1A>T (p.Met1Leu) rs561425038
NM_002878.4(RAD51D):c.263+1455del rs979233150
NM_002878.4(RAD51D):c.263+1507_263+1509del rs753760360
NM_002878.4(RAD51D):c.263+1596T>C rs1057517631
NM_002878.4(RAD51D):c.263+1597C>A rs755753106
NM_002878.4(RAD51D):c.270_271dup (p.Lys91fs) rs753862052
NM_002878.4(RAD51D):c.326dup (p.Gly110fs) rs730882119
NM_002878.4(RAD51D):c.339A>C (p.Lys113Asn) rs786202507
NM_002878.4(RAD51D):c.349T>A (p.Cys117Ser) rs786201358
NM_002878.4(RAD51D):c.478C>T (p.Gln160Ter) rs1057521922
NM_002878.4(RAD51D):c.6_13dup (p.Arg5fs) rs1555570506
NM_002878.4(RAD51D):c.740_741dup (p.Thr248Ter) rs1555567197
NM_002878.4(RAD51D):c.757C>A (p.Arg253=) rs137886232
NM_002878.4(RAD51D):c.757C>T (p.Arg253Ter) rs137886232
NM_002878.4(RAD51D):c.785C>T (p.Pro262Leu) rs730881950
NM_002878.4(RAD51D):c.81del (p.Val28fs) rs1064793952
NM_002878.4(RAD51D):c.85del (p.Val29fs) rs1057517586
NM_002878.4(RAD51D):c.94_95del (p.Val32fs) rs786203137

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.