RPGRIP1L NM_015272.5(RPGRIP1L):c.2682A>G (p.Ser894=)

CI-VAR-00054152Explore in graph →p.Ser894=NM_015272.5:c.2682A>GClinVar 319655 rs141608712

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
319655	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Nephronophthisis 8; Joubert syndrome 7; Meckel syndrome, type 5; Meckel-Gruber syndrome; Joubert syndrome; Lung cancer; Familial cancer of breast; COACH syndrome 3	germline	10	Oct 24, 2024	clinvar