Variant · Snv
GYS1 NM_002103.5(GYS1):c.1890G>A (p.Ala630=)
CI-VAR-00150974Explore in graph →p.Ala630=NM_002103.5:c.1890G>AClinVar 845147 rs142457302
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 845147 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Glycogen storage disease due to muscle and heart glycogen synthase deficiency; Sarcoma; Thyroid cancer, nonmedullary, 1 | germline | 3 | Oct 02, 2025 | clinvar |