KIF1A NM_001244008.2(KIF1A):c.364-14C>G

CI-VAR-00235235Explore in graph →NM_001244008.2:c.364-14C>GClinVar 1604700 rs376290711

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
1604700	Benign	criteria provided, multiple submitters, no conflicts	2	Hereditary spastic paraplegia 30; Intellectual disability, autosomal dominant 9; Neuropathy, hereditary sensory, type 2C; Uterine corpus endometrial carcinoma	germline	3	Jan 13, 2026	clinvar