Variant · Snv
TMC6 NM_001127198.5(TMC6):c.2021+11C>T
CI-VAR-00058680Explore in graph →NM_001127198.5:c.2021+11C>TClinVar 403544 rs143140501
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 |
|---|---|---|---|---|---|---|---|---|
| 403544 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Epidermodysplasia verruciformis; Uterine corpus endometrial carcinoma; Malignant lymphoma, large B-cell, diffuse; Lymphoma; Familial cancer of breast; Uterine carcinosarcoma; Thymoma; Acute myeloid leukemia; Malignant tumor of esophagus; Uveal melanoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Cervical cancer | germline | 5 | Feb 03, 2026 | clinvar |