PTCH2 NM_003738.5(PTCH2):c.2845_2846delinsAA (p.Ser949Asn) — variant · CancerIndex

Variant · Indel

PTCH2 NM_003738.5(PTCH2):c.2845_2846delinsAA (p.Ser949Asn)

CI-VAR-00313116Explore in graph →p.Ser949AsnNM_003738.5:c.2845_2846delinsAAClinVar 2716952 rs2521947481

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
2716952	Uncertain significance	criteria provided, single submitter	1	Gorlin syndrome	germline	1	Aug 18, 2023	clinvar