KAT5 NM_182710.3(KAT5):c.638T>G (p.Val213Gly)

CI-VAR-00013729Explore in graph →p.Val213GlyNM_182710.3:c.638T>GClinVar 55934 rs386834229

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
55934	not provided	no classification provided	0	Familial colorectal cancer	somatic	1	—	clinvar