TRNT1 NM_182916.3(TRNT1):c.107A>T (p.Glu36Val)

CI-VAR-00114760Explore in graph →p.Glu36ValNM_182916.3:c.107A>TClinVar 662894 rs138682354

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
662894	Uncertain significance	criteria provided, multiple submitters, no conflicts	2	Congenital sideroblastic anemia-B-cell immunodeficiency-periodic fever-developmental delay syndrome; Optic atrophy; Clear cell carcinoma of kidney; Ovarian serous cystadenocarcinoma	germline	5	Apr 23, 2026	clinvar