PMS2 NM_000535.7(PMS2):c.1020_1023delinsTTTC (p.Lys340_Arg341delinsAsnPhe) — variant · CancerIndex

Variant · Indel

PMS2 NM_000535.7(PMS2):c.1020_1023delinsTTTC (p.Lys340_Arg341delinsAsnPhe)

CI-VAR-00325785Explore in graph →p.Lys340_Arg341delinsAsnPheNM_000535.7:c.1020_1023delinsTTTCClinVar 2834943 rs2535937311

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
2834943	Uncertain significance	criteria provided, single submitter	1	Hereditary nonpolyposis colorectal neoplasms	germline	1	Mar 06, 2024	clinvar