Variant · Snv
NUP205 NM_015135.3(NUP205):c.1119G>A (p.Met373Ile)
CI-VAR-00199217Explore in graph →p.Met373IleNM_015135.3:c.1119G>AClinVar 1236909 rs61459701
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 |
|---|---|---|---|---|---|---|---|---|
| 1236909 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Lymphoma; Thymoma; Melanoma; Cholangiocarcinoma; Malignant lymphoma, large B-cell, diffuse; Sarcoma; Hepatocellular carcinoma; Cervical cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma; Ovarian cancer; Colon adenocarcinoma; Gastric cancer; Acute myeloid leukemia; Malignant tumor of esophagus; Familial cancer of breast | germline | 4 | Jul 15, 2024 | clinvar |