PDGFRA NM_006206.6(PDGFRA):c.1017_1019delinsTCA (p.Arg340Gln) — variant · CancerIndex

Variant · Indel

PDGFRA NM_006206.6(PDGFRA):c.1017_1019delinsTCA (p.Arg340Gln)

CI-VAR-00399517Explore in graph →p.Arg340GlnNM_006206.6:c.1017_1019delinsTCAClinVar 4665192

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
4665192	Benign/Likely benign	criteria provided, multiple submitters, no conflicts	2	Hereditary cancer-predisposing syndrome; Polyps, multiple and recurrent inflammatory fibroid, gastrointestinal	germline	2	Jun 16, 2026	clinvar