Variant · Snv
DNAJC6 NM_001256864.2(DNAJC6):c.194-19T>G
CI-VAR-00200757Explore in graph →NM_001256864.2:c.194-19T>GClinVar 1277678 rs2296479
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 |
|---|---|---|---|---|---|---|---|---|
| 1277678 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Juvenile onset Parkinson disease 19A; Malignant lymphoma, large B-cell, diffuse; Hepatocellular carcinoma; Pancreatic adenocarcinoma; Gastric cancer; Familial cancer of breast | germline | 5 | Feb 04, 2026 | clinvar |