KIF1C NM_006612.6(KIF1C):c.2299G>A (p.Gly767Arg)

CI-VAR-00068279Explore in graph →p.Gly767ArgNM_006612.6:c.2299G>AClinVar 424674 rs118037269

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
424674	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Hereditary spastic paraplegia; Spastic ataxia 2; KIF1C-related disorder; Colorectal cancer; Acute myeloid leukemia; Ovarian serous cystadenocarcinoma	germline	9	Jan 01, 2026	clinvar