Variant · Snv
ALK G1202R
CI-VAR-00001588Explore in graph →NP_004295.2:p.Gly1202ArgNM_004304.4:c.3604G>AClinVar 376134 CIViC 171 rs1057519783
Curated evidence
Evidence by cancer (13 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
- 22277784
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Lung Adenocarcinoma1 | ||||||||
| ALK G1202R AND v::ALK Fusion | Crizotinib | Predictive | C | Supports Resistance | 3 | accepted | EID1357A patient with ALK-rearranged lung adenocarcinoma responded to crizotinib treatment and then had relapse. Biopsy was taken within half a month and total DNA was extracted from the sample. Exons 20-28,… (full text at CIViC) PMID 22277784 · Katayama et al., 2012 · Open in CIViC | civic |
| Lung Non-Small Cell Carcinoma6 | ||||||||
| ALK G1202R AND v::ALK Fusion | Crizotinib | Predictive | C | Supports Resistance | 1 | submitted | EID4624In a non-small cell lung cancer patient with acquired crizotinib resistance, the tumor had an ALK gene rearrangement and an ALK G1202R co-mutation. The ALK G1202R tumor was reported to be refractory t… (full text at CIViC) PMID · | |
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 |
|---|---|---|---|---|---|---|---|---|
| 376134 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Lung cancer; Neuroblastoma, susceptibility to, 3; Hereditary cancer-predisposing syndrome | germline/somatic | 4 | Aug 19, 2025 | clinvar |