SPG11 NM_025137.4(SPG11):c.808G>A (p.Val270Ile)

CI-VAR-00008106Explore in graph →p.Val270IleNM_025137.4:c.808G>AClinVar 41366 rs80338868

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
41366	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary spastic paraplegia 11; Hereditary spastic paraplegia; Amyotrophic lateral sclerosis type 5; Inborn genetic diseases; Charcot-Marie-Tooth disease axonal type 2X; Neurofibromatosis, type 1	germline	17	Jun 01, 2026	clinvar