Variant · Snv
CHD1L NM_004284.6(CHD1L):c.2295A>G (p.Ile765Met)
CI-VAR-00234504Explore in graph →p.Ile765MetNM_004284.6:c.2295A>GClinVar 1627144 rs148289715
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 |
|---|---|---|---|---|---|---|---|---|
| 1627144 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | CHD1L-related disorder; Thyroid cancer, nonmedullary, 1; Melanoma; Malignant tumor of urinary bladder; Hepatocellular carcinoma; Clear cell carcinoma of kidney; Uveal melanoma; Colon adenocarcinoma; Gastric cancer; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma; Lung cancer; Cervical cancer; Familial cancer of breast | germline | 4 | Oct 01, 2025 | clinvar |