Variant · Snv
HDGFL2 NM_001001520.3(HDGFL2):c.1685A>G (p.Asn562Ser)
CI-VAR-00338562Explore in graph →p.Asn562SerNM_001001520.3:c.1685A>GClinVar 3024805 rs180870155
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 |
|---|---|---|---|---|---|---|---|---|
| 3024805 | Likely benign | criteria provided, single submitter | 1 | Clear cell carcinoma of kidney; Colon adenocarcinoma; Sarcoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Uterine corpus endometrial carcinoma; Cervical cancer; Familial cancer of breast; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Melanoma; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Malignant tumor of esophagus; Lung cancer | germline | 2 | Jan 01, 2024 | clinvar |