Variant · Snv
TMC6 NM_001127198.5(TMC6):c.2022-14G>A
CI-VAR-00196390Explore in graph →NM_001127198.5:c.2022-14G>AClinVar 1167298 rs188155233
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 1167298 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Epidermodysplasia verruciformis; Gastric cancer; Acute myeloid leukemia; Cervical cancer; Sarcoma; Ovarian serous cystadenocarcinoma | germline | 3 | Feb 04, 2026 | clinvar |