Variant · Snv
MCM6 NM_005915.6(MCM6):c.1082A>G (p.Asn361Ser)
CI-VAR-00338607Explore in graph →p.Asn361SerNM_005915.6:c.1082A>GClinVar 3033295 rs141448886
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 3033295 | Likely benign | criteria provided, single submitter | 1 | MCM6-related disorder; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Melanoma; Malignant tumor of esophagus; Malignant lymphoma, large B-cell, diffuse; Clear cell carcinoma of kidney; Gastric cancer; Lung cancer | germline | 3 | Nov 26, 2024 | clinvar |