Variant · Snv
TBC1D9B NM_015043.4(TBC1D9B):c.2420G>A (p.Arg807Gln)
CI-VAR-00306291Explore in graph →p.Arg807GlnNM_015043.4:c.2420G>AClinVar 2656141 rs145113784
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 |
|---|---|---|---|---|---|---|---|---|
| 2656141 | Benign | criteria provided, single submitter | 1 | Melanoma; Acute myeloid leukemia; Hepatocellular carcinoma; Malignant tumor of esophagus; Colon adenocarcinoma; Ovarian serous cystadenocarcinoma; Lung cancer; Sarcoma; Uterine carcinosarcoma; Adrenocortical carcinoma, hereditary; Familial cancer of breast | germline | 2 | Oct 01, 2022 | clinvar |