Variant · Snv
PSMD6 NM_014814.3(PSMD6):c.1021G>A (p.Gly341Arg)
CI-VAR-00294599Explore in graph →p.Gly341ArgNM_014814.3:c.1021G>AClinVar 2374128 rs140886939
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 |
|---|---|---|---|---|---|---|---|---|
| 2374128 | Uncertain significance | criteria provided, single submitter | 1 | Malignant lymphoma, large B-cell, diffuse; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma; Thyroid cancer, nonmedullary, 1; Melanoma; Hepatocellular carcinoma; Familial cancer of breast; Adrenocortical carcinoma, hereditary | germline | 2 | Aug 16, 2021 | clinvar |