Variant · Snv
DPM1 NM_003859.3(DPM1):c.679-7A>T
CI-VAR-00018180Explore in graph →NM_003859.3:c.679-7A>TClinVar 94380 rs60224379
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 |
|---|---|---|---|---|---|---|---|---|
| 94380 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital disorder of glycosylation type 1E; Uterine corpus endometrial carcinoma; Cholangiocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Lung cancer; Malignant lymphoma, large B-cell, diffuse; Gastric cancer; Familial cancer of breast; Sarcoma; Ovarian serous cystadenocarcinoma; Cervical cancer | germline | 10 | Feb 04, 2026 | clinvar |