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Gene | RAD51D |
Variant | S257_R259delinsK |
Impact List | indel |
Protein Effect | no effect |
Gene Variant Descriptions | RAD51D S257_R259delinsK results in a deletion of three amino acids combined with the insertion of a lysine (K) in the same location (UniProt.org). S257_R259delinsK, described as a reversion mutation, has no effect on Rad51d protein function, as demonstrated by restoration of homologous recombination function in cultured cells, and is associated with acquired resistance to PARP inhibitors (PMID: 28588062). |
Associated Drug Resistance | Y |
Category Variants Paths |
RAD51D mutant RAD51D S257_R259delinsK |
Transcript | NM_002878.4 |
gDNA | chr17:g.35101327_35101335delinsCTT |
cDNA | c.769_777delinsAAG |
Protein | p.S257_R259delinsK |
Source Database | RefSeq |
Genome Build | GRCh38/hg38 |
Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
---|---|---|---|---|---|
NM_002878.4 | chr17:g.35101327_35101335delinsCTT | c.769_777delinsAAG | p.S257_R259delinsK | RefSeq | GRCh38/hg38 |
NM_002878 | chr17:g.35101327_35101335delinsCTT | c.769_777delinsAAG | p.S257_R259delinsK | RefSeq | GRCh38/hg38 |
NM_002878.3 | chr17:g.35101327_35101335delinsCTT | c.769_777delinsAAG | p.S257_R259delinsK | RefSeq | GRCh38/hg38 |
Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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