Variant · Snv
DNAJC13 NM_015268.4(DNAJC13):c.5560+4A>T
CI-VAR-00198297Explore in graph →NM_015268.4:c.5560+4A>TClinVar 1210109 rs80120242
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 |
|---|---|---|---|---|---|---|---|---|
| 1210109 | Benign | criteria provided, multiple submitters, no conflicts | 2 | DNAJC13-related disorder; Acute myeloid leukemia; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Uveal melanoma; Lymphoma; Thymoma; Familial cancer of breast; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Uterine carcinosarcoma; Cholangiocarcinoma; Cervical cancer; Ovarian cancer; Familial pancreatic carcinoma; Malignant lymphoma, large B-cell, diffuse; Mesothelioma; Colorectal cancer | germline | 7 | Mar 24, 2022 | clinvar |