Variant · Snv
CSPP1 NM_001382391.1(CSPP1):c.3138A>G (p.Lys1046=)
CI-VAR-00056963Explore in graph →p.Lys1046=NM_001382391.1:c.3138A>GClinVar 379767 rs76567936
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 |
|---|---|---|---|---|---|---|---|---|
| 379767 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Joubert syndrome 21; Ovarian serous cystadenocarcinoma; Acute myeloid leukemia; Lung cancer; Cervical cancer; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Colorectal cancer; Uterine carcinosarcoma; Hepatocellular carcinoma | germline | 4 | Feb 01, 2026 | clinvar |