Variant · Snv
IFT52 NM_016004.5(IFT52):c.1011G>A (p.Ala337=)
CI-VAR-00198998Explore in graph →p.Ala337=NM_016004.5:c.1011G>AClinVar 1229501 rs41296223
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 |
|---|---|---|---|---|---|---|---|---|
| 1229501 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Lymphoma; Nonpapillary renal cell carcinoma; Thymoma; Cholangiocarcinoma; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Adrenocortical carcinoma, hereditary | germline | 4 | Jan 28, 2026 | clinvar |