Variant · Snv
PHB1 NM_002634.4(PHB1):c.128G>T (p.Arg43Leu)
CI-VAR-00377134Explore in graph →p.Arg43LeuNM_002634.4:c.128G>TClinVar 3770639
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 |
|---|---|---|---|---|---|---|---|---|
| 3770639 | Benign | criteria provided, single submitter | 1 | Thyroid cancer, nonmedullary, 1; Melanoma; Uterine corpus endometrial carcinoma; Clear cell carcinoma of kidney; Acute myeloid leukemia; Malignant tumor of esophagus; Colon adenocarcinoma; Colorectal cancer; Sarcoma; Gastric cancer; Uterine carcinosarcoma; Ovarian serous cystadenocarcinoma; Thymoma; Lung cancer; Nonpapillary renal cell carcinoma | germline | 2 | Dec 01, 2024 | clinvar |