Variant · Snv
SLC6A9 NM_001024845.3(SLC6A9):c.960C>T (p.Tyr320=)
CI-VAR-00072283Explore in graph →p.Tyr320=NM_001024845.3:c.960C>TClinVar 476370 rs61733181
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 |
|---|---|---|---|---|---|---|---|---|
| 476370 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Atypical glycine encephalopathy; Sarcoma; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Familial pancreatic carcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Cervical cancer | germline | 3 | Jan 27, 2026 | clinvar |