Variant · Snv
RNASEH1 NM_002936.6(RNASEH1):c.702A>G (p.Ala234=)
CI-VAR-00122518Explore in graph →p.Ala234=NM_002936.6:c.702A>GClinVar 673568 rs143510329
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 |
|---|---|---|---|---|---|---|---|---|
| 673568 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | RNASEH1-related disorder; Cervical cancer; Clear cell carcinoma of kidney; Melanoma; Nonpapillary renal cell carcinoma; Colon adenocarcinoma; Colorectal cancer; Gastric cancer; Ovarian serous cystadenocarcinoma; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma; Malignant tumor of esophagus; Lung cancer | germline | 7 | May 01, 2026 | clinvar |