Variant · Snv
PIK3CB NM_006219.3(PIK3CB):c.1932A>G (p.Gln644=)
CI-VAR-00128096Explore in graph →p.Gln644=NM_006219.3:c.1932A>GClinVar 723991 rs34601499
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 |
|---|---|---|---|---|---|---|---|---|
| 723991 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Gastric cancer; Hepatocellular carcinoma; Thyroid cancer, nonmedullary, 1; Ovarian serous cystadenocarcinoma; Malignant tumor of esophagus; Lung cancer; Malignant tumor of urinary bladder; Cervical cancer; Familial cancer of breast; Clear cell carcinoma of kidney; Colorectal cancer; Sarcoma | germline | 3 | Dec 31, 2019 | clinvar |