Variant · Insertion
PLCH2 NM_014638.4(PLCH2):c.2349+1_2349+9dup
CI-VAR-00132079Explore in graph →NM_014638.4:c.2349+1_2349+9dupClinVar 769500 rs142848828
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 |
|---|---|---|---|---|---|---|---|---|
| 769500 | Benign | criteria provided, single submitter | 1 | Papillary renal cell carcinoma type 1; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Clear cell carcinoma of kidney; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Familial pancreatic carcinoma | germline | 2 | Dec 18, 2019 | clinvar |