BRAF NM_004333.6(BRAF):c.1778_1779insATG (p.Gly593_Asp594insCys) — variant · CancerIndex

Variant · Insertion

BRAF NM_004333.6(BRAF):c.1778_1779insATG (p.Gly593_Asp594insCys)

CI-VAR-00242307Explore in graph →p.Gly593_Asp594insCysNM_004333.6:c.1778_1779insATGClinVar 1711072 rs2535999526

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
1711072	Uncertain significance	no assertion criteria provided	0	Prostate cancer, hereditary, 1	germline	1	Jul 29, 2022	clinvar