Variant · Snv
RAPSN NM_005055.5(RAPSN):c.*57C>T
CI-VAR-00052896Explore in graph →NM_005055.5:c.*57C>TClinVar 304968 rs45617144
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 |
|---|---|---|---|---|---|---|---|---|
| 304968 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital myasthenic syndrome 11; Fetal akinesia deformation sequence 1; Fetal akinesia deformation sequence 2; Nonpapillary renal cell carcinoma; Malignant lymphoma, large B-cell, diffuse; Thymoma; Acute myeloid leukemia | germline | 5 | Jul 10, 2021 | clinvar |