Variant · Snv
VPS13B NM_152564.5(VPS13B):c.3386A>G (p.Lys1129Arg)
CI-VAR-00018246Explore in graph →p.Lys1129ArgNM_152564.5:c.3386A>GClinVar 95845 rs61759485
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 95845 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Cohen syndrome; Inborn genetic diseases; VPS13B-related disorder; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Familial cancer of breast; Gastric cancer; Acute myeloid leukemia; Nonpapillary renal cell carcinoma | germline | 22 | Apr 01, 2026 | clinvar |