Variant · Snv
SLC19A1 NM_194255.4(SLC19A1):c.972G>A (p.Ala324=)
CI-VAR-00237362Explore in graph →p.Ala324=NM_194255.4:c.972G>AClinVar 1637940 rs79091853
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 |
|---|---|---|---|---|---|---|---|---|
| 1637940 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uveal melanoma; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Cervical cancer; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Thymoma; Melanoma | germline | 3 | Feb 02, 2026 | clinvar |