Variant · Snv
ACOT9 NM_001037171.2(ACOT9):c.934G>C (p.Glu312Gln)
CI-VAR-00395996Explore in graph →p.Glu312GlnNM_001037171.2:c.934G>CClinVar 4485156
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 |
|---|---|---|---|---|---|---|---|---|
| 4485156 | Benign | criteria provided, single submitter | 1 | Colon adenocarcinoma; Thymoma; Lymphoma; Ovarian cancer; Cholangiocarcinoma; Uterine corpus endometrial carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Clear cell carcinoma of kidney; Hepatocellular carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uterine carcinosarcoma; Gastric cancer; Cervical cancer; Acute myeloid leukemia; Nonpapillary renal cell carcinoma; Melanoma; Colorectal cancer; Malignant tumor of esophagus; Sarcoma; Familial pancreatic carcinoma | germline | 2 | Dec 02, 2021 | clinvar |