Variant · Deletion
FAM151A NM_176782.3(FAM151A):c.1003_1031del (p.Pro335fs)
CI-VAR-00126274Explore in graph →p.Pro335fsNM_176782.3:c.1003_1031delClinVar 773109 rs373739034
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
- 2026-09-24
- Retrieved
- Sep 29, 2026
- Layer
- normalized (units and labels harmonized; values unchanged)
- Evidence
- database
- License
- Public domain (US Government work, NCBI/NLM); acknowledgment requested
- Run
- ING-CLINVAR-20260929-000001
| Variation | Clinical significance | Review status | Stars | Conditions | Origin | Submitters | Last evaluated | Source |
|---|---|---|---|---|---|---|---|---|
| 773109 | Benign | criteria provided, single submitter | 1 | Hepatocellular carcinoma; Clear cell carcinoma of kidney; Colon adenocarcinoma; Lymphoma; Nonpapillary renal cell carcinoma | germline | 2 | Dec 21, 2019 | clinvar |