Variant · Snv
MAN1B1 NM_016219.5(MAN1B1):c.1761C>G (p.Val587=)
CI-VAR-00052237Explore in graph →p.Val587=NM_016219.5:c.1761C>GClinVar 365970 rs115889896
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 |
|---|---|---|---|---|---|---|---|---|
| 365970 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Rafiq syndrome; Inborn genetic diseases; Lung cancer; Cervical cancer; Familial cancer of breast; Uterine corpus endometrial carcinoma; Sarcoma; Acute myeloid leukemia; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma | germline | 5 | Dec 19, 2025 | clinvar |