Variant · Snv
MZT2A NM_001085365.2(MZT2A):c.171-3C>T
CI-VAR-00417528Explore in graph →NM_001085365.2:c.171-3C>TClinVar 4503901
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 |
|---|---|---|---|---|---|---|---|---|
| 4503901 | Benign | criteria provided, single submitter | 1 | Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Lymphoma; Cholangiocarcinoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer | germline | 2 | Nov 26, 2024 | clinvar |