Variant · Snv
RASA1 NM_002890.3(RASA1):c.1777-14T>A
CI-VAR-00033228Explore in graph →NM_002890.3:c.1777-14T>AClinVar 213658 rs36000817
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 |
|---|---|---|---|---|---|---|---|---|
| 213658 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Capillary malformation-arteriovenous malformation syndrome; Familial pancreatic carcinoma; Lymphoma; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Lung cancer; Cervical cancer; Uterine corpus endometrial carcinoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 5 | Feb 04, 2026 | clinvar |