Variant · Snv
PHKB NM_000293.3(PHKB):c.555G>T (p.Met185Ile)
CI-VAR-00031823Explore in graph →p.Met185IleNM_000293.3:c.555G>TClinVar 198067 rs56257827
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 |
|---|---|---|---|---|---|---|---|---|
| 198067 | Benign/Likely benign | criteria provided, multiple submitters, no conflicts | 2 | Glycogen storage disease IXb; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Gastric cancer; Lung cancer; Colon adenocarcinoma; Sarcoma; Ovarian serous cystadenocarcinoma; Nonpapillary renal cell carcinoma; Cervical cancer; Thyroid cancer, nonmedullary, 1; Melanoma; Acute myeloid leukemia; Malignant tumor of esophagus | germline | 15 | Jun 01, 2026 | clinvar |