Variant · Snv
PHGDH NM_006623.4(PHGDH):c.682G>T (p.Gly228Trp)
CI-VAR-00102949Explore in graph →p.Gly228TrpNM_006623.4:c.682G>TClinVar 581769 rs139063843
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 |
|---|---|---|---|---|---|---|---|---|
| 581769 | Conflicting classifications of pathogenicity | criteria provided, conflicting classifications | 1 | PHGDH deficiency; Neu-Laxova syndrome 1; PHGDH-related disorder; Malignant tumor of esophagus; Cervical cancer; Clear cell carcinoma of kidney | germline | 9 | Apr 29, 2026 | clinvar |