Variant · Snv
ANK1 NM_000037.4(ANK1):c.4385C>T (p.Ala1462Val)
CI-VAR-00047297Explore in graph →p.Ala1462ValNM_000037.4:c.4385C>TClinVar 261310 rs34664882
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 261310 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Hereditary spherocytosis type 1; Spherocytosis; Sarcoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Gastric cancer; Uterine carcinosarcoma; Malignant tumor of esophagus; Familial pancreatic carcinoma; Colorectal cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma | germline | 9 | Feb 01, 2026 | clinvar |