Variant · Snv
PSMF1 NM_006814.5(PSMF1):c.132G>A (p.Pro44=)
CI-VAR-00128445Explore in graph →p.Pro44=NM_006814.5:c.132G>AClinVar 732687 rs35517343
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 |
|---|---|---|---|---|---|---|---|---|
| 732687 | Benign | criteria provided, single submitter | 1 | Hepatocellular carcinoma; Malignant tumor of esophagus; Nonpapillary renal cell carcinoma; Cervical cancer; Clear cell carcinoma of kidney; Sarcoma; Thyroid cancer, nonmedullary, 1; Ovarian serous cystadenocarcinoma; Melanoma; Uterine corpus endometrial carcinoma | germline | 2 | May 24, 2018 | clinvar |