SLC25A46 NM_138773.4(SLC25A46):c.378A>G (p.Gln126=)

CI-VAR-00073963Explore in graph →p.Gln126=NM_138773.4:c.378A>GClinVar 475793 rs151055603

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
475793	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Neuropathy, hereditary motor and sensory, type 6B; Ovarian serous cystadenocarcinoma; Adrenocortical carcinoma, hereditary; Lung cancer; Colorectal cancer; Clear cell carcinoma of kidney	germline	6	Jun 01, 2026	clinvar