Variant · Snv
ATP11C NM_001353812.2(ATP11C):c.1556A>G (p.Tyr519Cys)
CI-VAR-00339163Explore in graph →p.Tyr519CysNM_001353812.2:c.1556A>GClinVar 3056300 rs17281983
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 |
|---|---|---|---|---|---|---|---|---|
| 3056300 | Benign | no assertion criteria provided | 0 | ATP11C-related disorder; Uterine corpus endometrial carcinoma; Malignant tumor of esophagus; Lung cancer; Clear cell carcinoma of kidney; Sarcoma; Ovarian serous cystadenocarcinoma; Thymoma | germline | 2 | Apr 30, 2019 | clinvar |