ERBB2 NM_004448.4(ERBB2):c.2332_2340dup (p.Gly778_Pro780dup) — variant · CancerIndex

Variant · Insertion

ERBB2 NM_004448.4(ERBB2):c.2332_2340dup (p.Gly778_Pro780dup)

CI-VAR-00008590Explore in graph →p.Gly778_Pro780dupNM_004448.4:c.2332_2340dupClinVar 44993 rs397516982

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
44993	Likely pathogenic	criteria provided, single submitter	1	Non-small cell lung carcinoma	somatic	1	Mar 06, 2013	clinvar