Variant · Snv
TCF4 NM_001083962.2(TCF4):c.1727G>A (p.Arg576Gln)
CI-VAR-00057809Explore in graph →p.Arg576GlnNM_001083962.2:c.1727G>AClinVar 381549 rs1057521070
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 |
|---|---|---|---|---|---|---|---|---|
| 381549 | Pathogenic | reviewed by expert panel | 3 | Pitt-Hopkins syndrome; Inborn genetic diseases; Medulloblastoma SHH activated; TCF4-related disorder | germline/somatic | 5 | Mar 26, 2021 | clinvar |