Variant · Snv
DSCAML1 NM_020693.4(DSCAML1):c.3237C>T (p.Ser1079=)
CI-VAR-00227227Explore in graph →p.Ser1079=NM_020693.4:c.3237C>TClinVar 1657706 rs61743159
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
- 2026-09-14
- Retrieved
- Sep 15, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260915-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1657706 | Benign | criteria provided, multiple submitters, no conflicts | 2 | DSCAML1-related disorder; Colon adenocarcinoma; Thyroid cancer, nonmedullary, 1; Melanoma; Clear cell carcinoma of kidney; Hepatocellular carcinoma; Nonpapillary renal cell carcinoma; Ovarian serous cystadenocarcinoma; Cervical cancer | germline | 4 | Feb 03, 2026 | clinvar |