Variant · Snv
CDK2AP2 NM_005851.5(CDK2AP2):c.180G>A (p.Gln60=)
CI-VAR-00126558Explore in graph →p.Gln60=NM_005851.5:c.180G>AClinVar 770402 rs144468375
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 |
|---|---|---|---|---|---|---|---|---|
| 770402 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Colon adenocarcinoma; Colorectal cancer; Sarcoma; Lymphoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Thymoma; Adrenocortical carcinoma, hereditary; Lung cancer; Uterine corpus endometrial carcinoma; Uveal melanoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Clear cell carcinoma of kidney; Malignant lymphoma, large B-cell, diffuse; Melanoma; Hepatocellular carcinoma; Cervical cancer | germline | 3 | Jul 31, 2018 | clinvar |