Variant · Snv
RPS3 NM_001005.5(RPS3):c.162-3C>T
CI-VAR-00132193Explore in graph →NM_001005.5:c.162-3C>TClinVar 769802 rs11236421
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 |
|---|---|---|---|---|---|---|---|---|
| 769802 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine carcinosarcoma; Melanoma; Acute myeloid leukemia; Malignant tumor of esophagus; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Uveal melanoma; Colon adenocarcinoma; Sarcoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Cervical cancer; Colorectal cancer; Gastric cancer; Lung cancer; Familial cancer of breast | germline | 3 | Jun 04, 2018 | clinvar |