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| Gene | PALB2 |
| Variant | T494Lfs*67 |
| Impact List | frameshift |
| Protein Effect | loss of function - predicted |
| Gene Variant Descriptions | PALB2 T494Lfs*67 indicates a shift in the reading frame starting at amino acid 494 and terminating 67 residues downstream causing a premature truncation of the 1186 amino acid Palb2 protein (UniProt.org). T494Lfs*67 has not been characterized, however, due to the effects of other Palb2 truncation mutations downstream of T494 (PMID: 31757951, PMID: 31636395), is predicted to lead to a loss of Palb2 protein function. |
| Associated Drug Resistance | |
| Category Variants Paths |
PALB2 mutant PALB2 inact mut PALB2 T494Lfs*67 |
| Transcript | NM_024675.4 |
| gDNA | chr16:g.23635066delT |
| cDNA | c.1480delA |
| Protein | p.T494Lfs*67 |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_001407297.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_001407298.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_001407300.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_001407299.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| XM_017023673.2 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_001407302.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_024675.3 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_024675.4 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| XM_017023672.2 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| NM_001407301.1 | chr16:g.23635066delT | c.1480delA | p.T494Lfs*67 | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
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