ClinVar Miner

Variants in gene combination RAD51D, RAD51L3-RFFL with conflicting interpretations reported as "benign and "likely benign"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status: Submission 2 (likely benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 24
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HGVS dbSNP gnomAD frequency
NM_002878.4(RAD51D):c.903+53C>T rs45496096 0.01225
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.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.919G>A (p.Glu307Lys) rs115031549 0.00083
NM_002878.4(RAD51D):c.904-11T>A rs374449943 0.00038
NM_002878.4(RAD51D):c.216C>T (p.Tyr72=) rs148690585 0.00028
NM_002878.4(RAD51D):c.983C>T (p.Thr328Ile) rs138969595 0.00021
NM_002878.4(RAD51D):c.904-3C>T rs45478491 0.00018
NM_002878.4(RAD51D):c.145-40C>T rs370850037 0.00011
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.346-10C>T rs779972784 0.00005
NM_002878.4(RAD51D):c.145-14G>C rs200470533 0.00004
NM_002878.4(RAD51D):c.792C>G (p.Leu264=) rs536544621 0.00002
NM_002878.4(RAD51D):c.198G>T (p.Val66=) rs200810304 0.00001
NM_002878.4(RAD51D):c.145-39G>T rs7207508
NM_002878.4(RAD51D):c.757C>A (p.Arg253=) rs137886232

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