Variant · Snv
MSR1 NM_138715.3(MSR1):c.103+1G>T
CI-VAR-00129464Explore in graph →NM_138715.3:c.103+1G>TClinVar 747968 rs150131889
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 |
|---|---|---|---|---|---|---|---|---|
| 747968 | Likely benign | criteria provided, multiple submitters, no conflicts | 2 | MSR1-related disorder; Papillary renal cell carcinoma type 1; Thyroid cancer, nonmedullary, 1; Familial cancer of breast; Clear cell carcinoma of kidney | germline | 4 | Jul 31, 2018 | clinvar |