HOXB13 NM_006361.6(HOXB13):c.366_369delinsTCGT (p.Ser122_Arg123=) — variant · CancerIndex

Variant · Indel

HOXB13 NM_006361.6(HOXB13):c.366_369delinsTCGT (p.Ser122_Arg123=)

CI-VAR-00377620Explore in graph →p.Ser122_Arg123=NM_006361.6:c.366_369delinsTCGTClinVar 3773168

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
3773168	Benign	criteria provided, single submitter	1	Prostate cancer, hereditary, 9	unknown	1	Oct 29, 2024	clinvar