Variant · Snv
AGRN NM_198576.4(AGRN):c.5223C>T (p.Gly1741=)
CI-VAR-00072104Explore in graph →p.Gly1741=NM_198576.4:c.5223C>TClinVar 474144 rs147681220
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 474144 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital myasthenic syndrome 8; AGRN-related disorder; Uterine corpus endometrial carcinoma; Colon adenocarcinoma; Sarcoma; Cervical cancer; Colorectal cancer; Gastric cancer; Lung cancer; Familial cancer of breast; Ovarian serous cystadenocarcinoma; Thymoma; Malignant tumor of urinary bladder; Malignant tumor of esophagus | germline | 8 | Apr 01, 2026 | clinvar |