Variant · Snv
ATR NM_001184.4(ATR):c.5931A>G (p.Gln1977=)
CI-VAR-00056456Explore in graph →p.Gln1977=NM_001184.4:c.5931A>GClinVar 382221 rs150964938
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 |
|---|---|---|---|---|---|---|---|---|
| 382221 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Inborn genetic diseases; Seckel syndrome 1; Familial cutaneous telangiectasia and oropharyngeal predisposition cancer syndrome; ATR-related disorder; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Lung cancer; Malignant lymphoma, large B-cell, diffuse; Thyroid cancer, nonmedullary, 1 | germline | 8 | Jan 15, 2026 | clinvar |