Variant · Snv
MAP3K6 NM_004672.5(MAP3K6):c.1256-2A>G
CI-VAR-00127863Explore in graph →NM_004672.5:c.1256-2A>GClinVar 718894 rs55841735
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 |
|---|---|---|---|---|---|---|---|---|
| 718894 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | MAP3K6-related disorder; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Melanoma; Familial cancer of breast; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Lymphoma; Thyroid cancer, nonmedullary, 1; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Uveal melanoma; Sarcoma | germline | 5 | Mar 01, 2023 | clinvar |