SLC25A21 NM_030631.4(SLC25A21):c.441A>G (p.Gln147=)

CI-VAR-00203340Explore in graph →p.Gln147=NM_030631.4:c.441A>GClinVar 1332980 rs17105087

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.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
1332980	Benign	criteria provided, multiple submitters, no conflicts	2	Mitochondrial DNA depletion syndrome 18; Malignant lymphoma, large B-cell, diffuse; Uterine carcinosarcoma; Uveal melanoma; Colorectal cancer; Adrenocortical carcinoma, hereditary	germline	4	Feb 02, 2026	clinvar