Variant · Snv
GALM NM_138801.3(GALM):c.147G>A (p.Gln49=)
CI-VAR-00200106Explore in graph →p.Gln49=NM_138801.3:c.147G>AClinVar 1259664 rs34708402
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 |
|---|---|---|---|---|---|---|---|---|
| 1259664 | Benign | criteria provided, multiple submitters, no conflicts | 2 | GALM-related disorder; Uterine corpus endometrial carcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Uterine carcinosarcoma; Lung cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Cervical cancer | germline | 5 | Feb 02, 2026 | clinvar |