Variant · Snv
CRYBB3 NM_004076.5(CRYBB3):c.38C>G (p.Ala13Gly)
CI-VAR-00054858Explore in graph →p.Ala13GlyNM_004076.5:c.38C>GClinVar 340949 rs147831812
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 |
|---|---|---|---|---|---|---|---|---|
| 340949 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Cataract 22 multiple types; Inborn genetic diseases; Gastric cancer; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Clear cell carcinoma of kidney | germline | 4 | Nov 17, 2025 | clinvar |