Variant · Snv
EFCAB13 NM_152347.5(EFCAB13):c.806-1G>A
CI-VAR-00339284Explore in graph →NM_152347.5:c.806-1G>AClinVar 3055475 rs76299620
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 |
|---|---|---|---|---|---|---|---|---|
| 3055475 | Benign | no assertion criteria provided | 0 | EFCAB13-related disorder; Sarcoma; Thymoma; Cervical cancer; Melanoma; Acute myeloid leukemia; Uterine corpus endometrial carcinoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Lung cancer | germline | 2 | Sep 30, 2019 | clinvar |