Variant · Snv
MAP4 NM_001385682.1(MAP4):c.292+9T>G
CI-VAR-00132349Explore in graph →NM_001385682.1:c.292+9T>GClinVar 790262 rs182500657
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 |
|---|---|---|---|---|---|---|---|---|
| 790262 | Benign | criteria provided, multiple submitters, no conflicts | 2 | MAP4-related disorder; Clear cell carcinoma of kidney; Cervical cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Malignant lymphoma, large B-cell, diffuse; Acute myeloid leukemia | germline | 4 | Dec 31, 2019 | clinvar |