KIF1A NM_001244008.2(KIF1A):c.234C>T (p.Gly78=)

CI-VAR-00020410Explore in graph →p.Gly78=NM_001244008.2:c.234C>TClinVar 129386 rs61744930

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
129386	Benign	criteria provided, multiple submitters, no conflicts	2	Hereditary spastic paraplegia 30; Neuropathy, hereditary sensory, type 2C; Intellectual disability, autosomal dominant 9; Hereditary spastic paraplegia; Inborn genetic diseases; Ovarian serous cystadenocarcinoma; Uterine corpus endometrial carcinoma; Uterine carcinosarcoma	germline	10	Feb 03, 2026	clinvar