Variant · Snv
PRRC2C NM_001387844.1(PRRC2C):c.1035C>G (p.Asn345Lys)
CI-VAR-00294312Explore in graph →p.Asn345LysNM_001387844.1:c.1035C>GClinVar 2349221 rs36013361
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 |
|---|---|---|---|---|---|---|---|---|
| 2349221 | Uncertain significance | criteria provided, single submitter | 1 | Colon adenocarcinoma; Gastric cancer; Thyroid cancer, nonmedullary, 1; Malignant tumor of esophagus | germline | 2 | Sep 10, 2025 | clinvar |