Variant · Snv
CYP2D6 NM_000106.6(CYP2D6):c.975G>A (p.Pro325=)
CI-VAR-00306196Explore in graph →p.Pro325=NM_000106.6:c.975G>AClinVar 2653240 rs79292917
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 |
|---|---|---|---|---|---|---|---|---|
| 2653240 | Likely benign | criteria provided, single submitter | 1 | Malignant lymphoma, large B-cell, diffuse; Glioma susceptibility 1; Colorectal cancer; Cholangiocarcinoma; Malignant tumor of esophagus; Lung cancer; Familial cancer of breast | germline | 2 | Jun 01, 2022 | clinvar |