Variant · Snv
ZFYVE27 NM_001385875.1(ZFYVE27):c.572G>T (p.Gly191Val)
CI-VAR-00005225Explore in graph →p.Gly191ValNM_001385875.1:c.572G>TClinVar 1289 rs35077384
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 |
|---|---|---|---|---|---|---|---|---|
| 1289 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | Hereditary spastic paraplegia 33; Spastic tetraparesis; Spastic paraplegia; Ovarian serous cystadenocarcinoma; Thymoma; Uveal melanoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Colon adenocarcinoma; Colorectal cancer; Cervical cancer; Sarcoma; Thyroid cancer, nonmedullary, 1; Uterine corpus endometrial carcinoma; Melanoma; Cholangiocarcinoma; Gastric cancer; Uterine carcinosarcoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer | germline | 12 | Jan 27, 2026 | clinvar |