Variant · Snv
ALG13 NM_001099922.3(ALG13):c.183C>T (p.Tyr61=)
CI-VAR-00045811Explore in graph →p.Tyr61=NM_001099922.3:c.183C>TClinVar 238290 rs146925326
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 |
|---|---|---|---|---|---|---|---|---|
| 238290 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Developmental and epileptic encephalopathy, 36; Inborn genetic diseases; Lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Sarcoma; Acute myeloid leukemia; Malignant tumor of esophagus; Familial cancer of breast; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Uveal melanoma; Familial pancreatic carcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Colorectal cancer; Gastric cancer; Melanoma; Hepatocellular carcinoma; Ovarian cancer | germline | 7 | Feb 03, 2026 | clinvar |