ERBB2 NM_004448.4(ERBB2):c.2325_2326insTCCGTGATGGCT (p.Ala775_Gly776insSerValMetAla) — variant · CancerIndex

Variant · Insertion

ERBB2 NM_004448.4(ERBB2):c.2325_2326insTCCGTGATGGCT (p.Ala775_Gly776insSerValMetAla)

CI-VAR-00025831Explore in graph →p.Ala775_Gly776insSerValMetAlaNM_004448.4:c.2325_2326insTCCGTGATGGCTClinVar 163409 rs1555618025

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
163409	Likely pathogenic	criteria provided, single submitter	1	Non-small cell lung carcinoma	somatic	1	Aug 19, 2013	clinvar