PEX10 NM_002617.4(PEX10):c.279C>T (p.Gly93=)

CI-VAR-00020449Explore in graph →p.Gly93=NM_002617.4:c.279C>TClinVar 129883 rs1143016

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
129883	Benign	criteria provided, multiple submitters, no conflicts	2	Peroxisome biogenesis disorder 6A (Zellweger); Peroxisome biogenesis disorder, complementation group 7; Peroxisome biogenesis disorder 6B; Zellweger spectrum disorders; Acute myeloid leukemia; Adrenocortical carcinoma, hereditary; Colorectal cancer; Thymoma; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma	germline	12	Feb 04, 2026	clinvar