Variant · Snv
LRPPRC NM_133259.4(LRPPRC):c.3570-3C>T
CI-VAR-00022436Explore in graph →NM_133259.4:c.3570-3C>TClinVar 138153 rs35113761
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 |
|---|---|---|---|---|---|---|---|---|
| 138153 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Congenital lactic acidosis, Saguenay-Lac-Saint-Jean type; Sarcoma; Lymphoma; Uterine carcinosarcoma; Thymoma; Uterine corpus endometrial carcinoma; Chronic lymphocytic leukemia/small lymphocytic lymphoma; Nonpapillary renal cell carcinoma; Adrenocortical carcinoma, hereditary; Ovarian cancer; Familial pancreatic carcinoma; Colorectal cancer; Melanoma; Acute myeloid leukemia; Uveal melanoma; Colon adenocarcinoma; Cholangiocarcinoma; Malignant tumor of esophagus | germline | 9 | Feb 04, 2026 | clinvar |