MFN2 NM_014874.4(MFN2):c.1452G>A (p.Thr484=)

CI-VAR-00031662Explore in graph →p.Thr484=NM_014874.4:c.1452G>AClinVar 194409 rs150043585

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
194409	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Charcot-Marie-Tooth disease type 2; Hereditary motor and sensory neuropathy with optic atrophy; Charcot-Marie-Tooth disease; Inborn genetic diseases; Melanoma; Thyroid cancer, nonmedullary, 1	germline	15	Jan 27, 2026	clinvar