Variant · Snv
TMEM94 NM_014738.6(TMEM94):c.2087-5C>G
CI-VAR-00201445Explore in graph →NM_014738.6:c.2087-5C>GClinVar 1300064 rs4078474
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 |
|---|---|---|---|---|---|---|---|---|
| 1300064 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Intellectual developmental disorder with cardiac defects and dysmorphic facies; Hepatocellular carcinoma; Germ cell tumor of testis | germline | 4 | Nov 28, 2024 | clinvar |