Variant · Deletion
MAP3K20 NM_016653.3(MAP3K20):c.1360-14_1360-9del
CI-VAR-00199028Explore in graph →NM_016653.3:c.1360-14_1360-9delClinVar 1229230 rs150855284
Curated evidence
Evidence by cancer (0 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.
Data not yet available
No curated evidence item references this variant yet.
ClinVar
Clinical significance (1)
ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.
clinvarProvenance
- Source
- NCBI ClinVar (variant_summary)
- Dataset
- ClinVar variant_summary
- Version
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1229230 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Myopathy, centronuclear, 6, with fiber-type disproportion; Split-foot malformation-mesoaxial polydactyly syndrome; Gastric cancer; Lymphoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Malignant lymphoma, large B-cell, diffuse; Cervical cancer | germline | 4 | Feb 03, 2026 | clinvar |