Variant · Snv
GSTP1 NM_000852.4(GSTP1):c.341C>T (p.Ala114Val)
CI-VAR-00006668Explore in graph →p.Ala114ValNM_000852.4:c.341C>TClinVar 1264275 rs1138272
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1264275 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Pulmonary disease, chronic obstructive, susceptibility to; Colon adenocarcinoma; Uterine carcinosarcoma; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Uveal melanoma; Thymoma; Cholangiocarcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma | germline | 4 | Jun 09, 2021 | clinvar |