Variant · Snv
RECQL5 NM_004259.7(RECQL5):c.1586-7C>A
CI-VAR-00339200Explore in graph →NM_004259.7:c.1586-7C>AClinVar 3059997 rs113150921
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 |
|---|---|---|---|---|---|---|---|---|
| 3059997 | Benign | no assertion criteria provided | 0 | RECQL5-related disorder; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Gastric cancer; Malignant lymphoma, large B-cell, diffuse; Ovarian serous cystadenocarcinoma; Cholangiocarcinoma; Hepatocellular carcinoma; Lung cancer; Familial cancer of breast | germline | 2 | Oct 30, 2019 | clinvar |