Variant · Snv
ABCG1 NM_016818.3(ABCG1):c.993C>T (p.Gly331=)
CI-VAR-00338940Explore in graph →p.Gly331=NM_016818.3:c.993C>TClinVar 3037791 rs56140811
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 |
|---|---|---|---|---|---|---|---|---|
| 3037791 | Benign | no assertion criteria provided | 0 | ABCG1-related disorder; Colon adenocarcinoma; Uterine corpus endometrial carcinoma; Sarcoma; Malignant tumor of esophagus; Cervical cancer; Adrenocortical carcinoma, hereditary; Uterine carcinosarcoma; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Uveal melanoma; Colorectal cancer; Nonpapillary renal cell carcinoma; Lung cancer | germline | 2 | Oct 28, 2019 | clinvar |