Variant · Snv
SCARB1 NM_005505.5(SCARB1):c.501C>T (p.Gly167=)
CI-VAR-00200820Explore in graph →p.Gly167=NM_005505.5:c.501C>TClinVar 1283188 rs5889
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1283188 | Benign | criteria provided, multiple submitters, no conflicts | 2 | SCARB1-related disorder; Melanoma; Cholangiocarcinoma; Acute myeloid leukemia; Adrenocortical carcinoma, hereditary; Lung cancer; Sarcoma; Thymoma; Malignant lymphoma, large B-cell, diffuse; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney | germline | 5 | Feb 03, 2026 | clinvar |