Variant · Indel
CTC1 NM_025099.6(CTC1):c.1078-4_1078-3delinsTT
CI-VAR-00205094Explore in graph →NM_025099.6:c.1078-4_1078-3delinsTTClinVar 1523519 rs2151522382
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 |
|---|---|---|---|---|---|---|---|---|
| 1523519 | Uncertain significance | criteria provided, multiple submitters, no conflicts | 2 | Dyskeratosis congenita; Cerebroretinal microangiopathy with calcifications and cysts 1 | germline | 2 | Jan 19, 2024 | clinvar |