Variant · Snv
MAP2K1 Q56P
CI-VAR-00003553Explore in graph →NP_002746.1:p.Gln56ProNM_002755.3:c.167A>CClinVar 375978 CIViC 83 rs1057519729
Curated evidence
Evidence by cancer (3 items)
Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.
- Source
- CIViC — Clinical Interpretation of Variants in Cancer
- Dataset
- CIViC evidence items
- Version
- civic-2026-09-08
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- expert curation
- License
- CC0 1.0
- PMID
- 19915144
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Melanoma2 | ||||||||
| MAP2K1 Q56P | Selumetinib | Predictive | D | Supports Resistance | 3 | accepted | EID13A375 cells expressing MAP2K1 Q56P mutation conferred an approximately 100-fold increased resistance to selumetinib (AZD6244) induced growth inhibition when compared to untransduced cells, cells expres… (full text at CIViC) PMID 19915144 · Emery et al., 2009 · Open in CIViC | civic |
| MAP2K1 Q56P | Vemurafenib | Predictive | C | Supports Resistance | — | submitted | EID4727In a retrospective study of a phase 2 clinical trial (NCT00949702), of 132 BRAF mutation positive metastatic melanoma patients treated with vemurafenib monotherapy, the MAP2K1 Q56P mutation was associ… (full text at CIViC) PMID 23569304 · Trunzer et al., 2013 · Open in CIViC | civic |
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 375978 | Pathogenic | criteria provided, multiple submitters, no conflicts | 2 | Non-small cell lung carcinoma; Melorheostosis; Neoplasm; Extracranial arteriovenous malformation | germline/somatic | 5 | May 15, 2024 | clinvar |