Variant · Snv
SAMD12 NM_207506.3(SAMD12):c.320C>T (p.Thr107Ile)
CI-VAR-00306212Explore in graph →p.Thr107IleNM_207506.3:c.320C>TClinVar 2658776 rs117020479
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 |
|---|---|---|---|---|---|---|---|---|
| 2658776 | Likely benign | criteria provided, single submitter | 1 | Familial pancreatic carcinoma; Gastric cancer; Hepatocellular carcinoma; Lung cancer; Ovarian cancer; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Colon adenocarcinoma; Malignant tumor of esophagus; Familial cancer of breast; Lymphoma; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1 | germline | 2 | Aug 01, 2025 | clinvar |