Variant · Snv
ACADVL NM_000018.4(ACADVL):c.49C>T (p.Leu17Phe)
CI-VAR-00006520Explore in graph →p.Leu17PheNM_000018.4:c.49C>TClinVar 21022 rs2230179
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 21022 | Benign | reviewed by expert panel | 3 | Very long chain acyl-CoA dehydrogenase deficiency; Clear cell carcinoma of kidney; Colorectal cancer; Nonpapillary renal cell carcinoma; Colon adenocarcinoma; Gastric cancer; Malignant tumor of esophagus; Lung cancer; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Acute myeloid leukemia; Uterine corpus endometrial carcinoma | germline | 15 | Sep 22, 2022 | clinvar |