TRAPPC9 NM_001160372.4(TRAPPC9):c.1019C>T (p.Ala340Val)

CI-VAR-00020502Explore in graph →p.Ala340ValNM_001160372.4:c.1019C>TClinVar 130612 rs143778652

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
130612	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Intellectual disability, autosomal recessive 13; Intellectual disability; Inborn genetic diseases; Acute myeloid leukemia	germline	8	Jul 08, 2023	clinvar