Variant
RET CLD1 Mutation
CI-VAR-00000381Explore in graph →CIViC 4697
Curated evidence
Evidence by cancer (1 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.
civicProvenance
- 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
- 32284345
- Run
- ING-CIVIC-20260908-000001
| Molecular profile | Therapy | Type | Level | Direction · significance | Rating (1–5) | Status | Evidence | Source |
|---|---|---|---|---|---|---|---|---|
| Solid Neoplasm1 | ||||||||
| RET CLD1 Mutation | (oncogenic) | Oncogenic | B | Supports Oncogenicity | 1 | submitted | EID11722560 of 37,056 patients from hospitals across China were found to contain RET mutations with the prevalence highest in thyroid cancer (6.45%), mediastinal tumor (7.69%), uterine cancer (3.94%), urinary… (full text at CIViC) PMID 32284345 · Zhao et al., 2020 · Open in CIViC | civic |
ClinVar
Clinical significance (0)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
Data not yet available
No ClinVar interpretation attached to this variant.