Missing content? – Request curation!
Request curation for specific Genes, Variants, or PubMed publications.
Have questions, comments, or suggestions? - Let us know!
Email us at : ckbsupport@genomenon.com
| Gene | STK11 |
| Variant | W332* |
| Impact List | nonsense |
| Protein Effect | unknown |
| Gene Variant Descriptions | STK11 W332* results in a premature truncation of the Stk11 protein at amino acid 332 of 433 (UniProt.org). W332* has been identified in sequencing studies (PMID: 17711506, PMID: 27923066, PMID: 28978051), but has not been biochemically characterized and therefore, its effect on Stk11 protein function is unknown (PubMed, Oct 2025). |
| Associated Drug Resistance | |
| Category Variants Paths |
STK11 mutant STK11 W332* |
| Transcript | NM_000455.5 |
| gDNA | chr19:g.1223059G>A |
| cDNA | c.995G>A |
| Protein | p.W332* |
| Source Database | RefSeq |
| Genome Build | GRCh38/hg38 |
| Transcript | gDNA | cDNA | Protein | Source Database | Genome Build |
|---|---|---|---|---|---|
| NM_000455.4 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| NM_000455.5 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| NM_000455 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| XM_005259617 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| XM_005259617.3 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| XM_005259618.3 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| NM_001407255.1 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| XM_005259618 | chr19:g.1223059G>A | c.995G>A | p.W332* | RefSeq | GRCh38/hg38 |
| Molecular Profile | Indication/Tumor Type | Response Type | Therapy Name | Approval Status | Evidence Type | Efficacy Evidence | References |
|---|---|---|---|---|---|---|---|
| STK11 W332* | lung non-small cell carcinoma | sensitive | Trametinib | Preclinical - Cell culture | Actionable | In a preclinical study, non-small cell lung cancer cell lines harboring STK11 inactivating mutations, such as STK11 W332*, demonstrated increased sensitivity to Mekinist (trametinib) in culture (PMID: 27821489). | 27821489 |