Variant · Snv
HYI NM_001190880.3(HYI):c.505+5G>A
CI-VAR-00071682Explore in graph →NM_001190880.3:c.505+5G>AClinVar 445670 rs111686948
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 |
|---|---|---|---|---|---|---|---|---|
| 445670 | Likely benign | criteria provided, single submitter | 1 | Thymoma; Melanoma; Cervical cancer; Clear cell carcinoma of kidney; Colon adenocarcinoma; Sarcoma; Gastric cancer; Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Lung cancer; Uterine corpus endometrial carcinoma; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1 | germline | 2 | Aug 08, 2017 | clinvar |