TP53 NM_000546.6(TP53):c.1024C>T (p.Arg342Ter)

CI-VAR-00026937Explore in graph →p.Arg342TerNM_000546.6:c.1024C>TClinVar 182970 rs730882029

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
182970	Pathogenic	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Li-Fraumeni syndrome; Ovarian neoplasm; Gallbladder cancer; Colonic diverticula; Li-Fraumeni syndrome 1; Adrenocortical carcinoma, hereditary; TP53-related disorder; Neoplasm; Diffuse glioma, H3 G34 mutant; Medulloblastoma SHH activated; Diffuse midline glioma, H3 K27M-mutant; Primary intracranial sarcoma, DICER1-mutant	germline/somatic	28	Aug 03, 2026	clinvar