Variant · Snv
ADCK2 NM_052853.4(ADCK2):c.933+1G>C
CI-VAR-00338938Explore in graph →NM_052853.4:c.933+1G>CClinVar 3037734 rs140400082
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 |
|---|---|---|---|---|---|---|---|---|
| 3037734 | Likely benign | criteria provided, single submitter | 1 | ADCK2-related disorder; Familial pancreatic carcinoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Sarcoma; Malignant tumor of urinary bladder; Uveal melanoma; Cervical cancer; Adrenocortical carcinoma, hereditary; Familial cancer of breast; Lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Papillary renal cell carcinoma type 1; Colon adenocarcinoma; Gastric cancer; Thyroid cancer, nonmedullary, 1; Hepatocellular carcinoma; Lung cancer | germline | 3 | Aug 01, 2025 | clinvar |