Variant · Snv
MDH2 NM_005918.4(MDH2):c.429G>A (p.Pro143=)
CI-VAR-00237735Explore in graph →p.Pro143=NM_005918.4:c.429G>AClinVar 1673616 rs11538801
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 |
|---|---|---|---|---|---|---|---|---|
| 1673616 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Chronic lymphocytic leukemia/small lymphocytic lymphoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Melanoma; Cholangiocarcinoma; Uveal melanoma; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Sarcoma; Adrenocortical carcinoma, hereditary; Lung cancer; Cervical cancer; Ovarian cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Lymphoma; Uterine carcinosarcoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 5 | Feb 03, 2026 | clinvar |