Variant · Snv
ALG14 NM_144988.4(ALG14):c.137-18T>A
CI-VAR-00093242Explore in graph →NM_144988.4:c.137-18T>AClinVar 516659 rs12751061
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 |
|---|---|---|---|---|---|---|---|---|
| 516659 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital myasthenic syndrome 15; Intellectual developmental disorder with epilepsy, behavioral abnormalities, and coarse facies; Myopathy, epilepsy, and progressive cerebral atrophy; Uveal melanoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uterine carcinosarcoma; Cholangiocarcinoma; Thymoma; Nonpapillary renal cell carcinoma | germline | 6 | Feb 03, 2026 | clinvar |