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Items: 12

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RAD51D, RAD51L3-RFFL
(Q319* +2 more)
Single nucleotide variant
(nonsense +1 more)
not provided
+3 more
GUncertain significance
RAD51D, RAD51L3-RFFL
(E307K +2 more)
Single nucleotide variant
(missense variant +1 more)
RAD51D-related condition
+5 more
GConflicting classifications of pathogenicity
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(synonymous variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
RAD51D, RAD51L3-RFFL
(E233G +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary cancer-predisposing syndrome
+3 more
GBenign/Likely benign
RAD51D, RAD51L3-RFFL
(A190T +2 more)
Single nucleotide variant
(non-coding transcript variant +1 more)
Hereditary cancer
+5 more
GConflicting classifications of pathogenicity
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(intron variant)
Breast and/or ovarian cancer
+4 more
GBenign/Likely benign
RAD51D, RAD51L3-RFFL
(R145H +1 more)
Single nucleotide variant
(missense variant +2 more)
RAD51D-related condition
+3 more
GUncertain significance
RAD51D, RAD51L3-RFFL
(G130fs +1 more)
Duplication
(non-coding transcript variant +2 more)
Hereditary cancer-predisposing syndrome
+2 more
GPathogenic
RAD51D, RAD51L3-RFFL
Single nucleotide variant
(synonymous variant +1 more)
not provided
+3 more
GBenign
RAD51D, RAD51L3-RFFL
(A49V)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer-predisposing syndrome
+4 more
GConflicting classifications of pathogenicity
RAD51L3-RFFL, RAD51D
(C9S)
Single nucleotide variant
(missense variant +1 more)
Hereditary cancer
+6 more
GConflicting classifications of pathogenicity
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