PEX6 NM_000287.4(PEX6):c.617G>A (p.Gly206Glu)

CI-VAR-00049844Explore in graph →p.Gly206GluNM_000287.4:c.617G>AClinVar 289831 rs139093654

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
289831	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Zellweger spectrum disorders; Peroxisome biogenesis disorder; Heimler syndrome 2; Peroxisome biogenesis disorder 4A (Zellweger); Peroxisome biogenesis disorder 4B; Familial cancer of breast; Clear cell carcinoma of kidney	germline	6	Jul 17, 2023	clinvar