Variant · Snv
MPC1 NM_016098.4(MPC1):c.303C>T (p.His101=)
CI-VAR-00022444Explore in graph →p.His101=NM_016098.4:c.303C>TClinVar 138241 rs12205572
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
- 2026-09-06
- Retrieved
- Sep 8, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260908-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 138241 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Uterine corpus endometrial carcinoma; Uveal melanoma; Lymphoma; Cholangiocarcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Thymoma; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Cervical cancer; Familial cancer of breast; Ovarian cancer; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Colon adenocarcinoma; Colorectal cancer | germline | 4 | Feb 03, 2026 | clinvar |