CC2D2A NM_001378615.1(CC2D2A):c.3055C>T (p.Arg1019Ter)

CI-VAR-00034485Explore in graph →p.Arg1019TerNM_001378615.1:c.3055C>TClinVar 217602 rs370880399

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
217602	Pathogenic/Likely pathogenic	criteria provided, multiple submitters, no conflicts	2	Joubert syndrome 9; COACH syndrome 1; Meckel syndrome, type 6; Meckel-Gruber syndrome; Joubert syndrome; CC2D2A-related disorder; Retinitis pigmentosa 93; COACH syndrome 2; Clear cell carcinoma of kidney	germline	13	Jan 19, 2026	clinvar