Variant · Snv
RASA2 NM_006506.5(RASA2):c.2016T>C (p.Asn672=)
CI-VAR-00092588Explore in graph →p.Asn672=NM_006506.5:c.2016T>CClinVar 496321 rs295322
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 |
|---|---|---|---|---|---|---|---|---|
| 496321 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Malignant lymphoma, large B-cell, diffuse; Lymphoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uveal melanoma; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Ovarian cancer; Familial pancreatic carcinoma; Colorectal cancer | germline | 6 | Feb 04, 2026 | clinvar |