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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(intron variant)
Breast-ovarian cancer, familial, susceptibility to, 4
+3 more
GConflicting classifications of pathogenicity
RAD51D, RAD51L3-RFFL
(R266C +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Breast-ovarian cancer, familial, susceptibility to, 4
+6 more
GConflicting classifications of pathogenicity
RAD51L3-RFFL, RAD51D
(R232* +2 more)
Single nucleotide variant
(nonsense +1 more)
Colorectal cancer
+5 more
GPathogenic/Likely pathogenic
RAD51D, RAD51L3-RFFL
(S207L +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not provided
+4 more
GConflicting classifications of pathogenicity
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(intron variant)
Breast-ovarian cancer, familial, susceptibility to, 4
+1 more
GConflicting classifications of pathogenicity
RAD51L3-RFFL, RAD51D
(R165Q +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
not specified
+3 more
GBenign
RAD51D, RAD51L3-RFFL
(Q151* +1 more)
Single nucleotide variant
(nonsense +2 more)
Hereditary cancer-predisposing syndrome
+3 more
GPathogenic/Likely pathogenic
RAD51L3-RFFL, RAD51D
Single nucleotide variant
(splice acceptor variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GPathogenic/Likely pathogenic
RAD51D, RAD51L3-RFFL
(A80V)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+1 more
GUncertain significance
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