KMT2D NM_003482.4(KMT2D):c.11796ACAGCAGCA[1] (p.Gln3937_Gln3939del) — variant · CancerIndex

Variant · Other

KMT2D NM_003482.4(KMT2D):c.11796ACAGCAGCA[1] (p.Gln3937_Gln3939del)

CI-VAR-00203672Explore in graph →p.Gln3937_Gln3939delNM_003482.4:c.11796ACAGCAGCA[1]ClinVar 1338410 rs759803583

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
1338410	Conflicting classifications of pathogenicity	criteria provided, conflicting classifications	1	Kabuki syndrome; Primary central nervous system lymphoma	germline/somatic	4	Oct 01, 2025	clinvar