PTCH1 NM_001083603.3(PTCH1):c.130GAA[6] (p.Glu48_Asn49insGlu) — variant · CancerIndex

Variant · Other

PTCH1 NM_001083603.3(PTCH1):c.130GAA[6] (p.Glu48_Asn49insGlu)

CI-VAR-00240885Explore in graph →p.Glu48_Asn49insGluNM_001083603.3:c.130GAA[6]ClinVar 1692540 rs112914470

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
1692540	Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome	germline	5	Dec 29, 2025	clinvar