Variant · Snv
LAMB3 NM_000228.3(LAMB3):c.2554A>T (p.Met852Leu)
CI-VAR-00047033Explore in graph →p.Met852LeuNM_000228.3:c.2554A>TClinVar 255588 rs12748250
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 |
|---|---|---|---|---|---|---|---|---|
| 255588 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Junctional epidermolysis bullosa; Amelogenesis imperfecta type 1A; Junctional epidermolysis bullosa gravis of Herlitz; Junctional epidermolysis bullosa, non-Herlitz type; Familial pancreatic carcinoma; Colorectal cancer; Ovarian cancer; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Familial cancer of breast | germline | 9 | Feb 04, 2026 | clinvar |