Variant · Snv
SNX19 NM_014758.3(SNX19):c.2444G>C (p.Gly815Ala)
CI-VAR-00127107Explore in graph →p.Gly815AlaNM_014758.3:c.2444G>CClinVar 786927 rs61759531
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 |
|---|---|---|---|---|---|---|---|---|
| 786927 | Benign | criteria provided, multiple submitters, no conflicts | 2 | Sarcoma; Gastric cancer; Ovarian serous cystadenocarcinoma; Thymoma; Thyroid cancer, nonmedullary, 1; Uterine corpus endometrial carcinoma; Nonpapillary renal cell carcinoma; Lung cancer; Cervical cancer; Familial cancer of breast; Malignant lymphoma, large B-cell, diffuse; Colorectal cancer; Clear cell carcinoma of kidney; Colon adenocarcinoma; Acute myeloid leukemia; Malignant tumor of esophagus; Melanoma; Hepatocellular carcinoma | germline | 3 | Dec 31, 2019 | clinvar |