MED12L NM_001393769.1(MED12L):c.5647A>G (p.Thr1883Ala)

CI-VAR-00294772Explore in graph →p.Thr1883AlaNM_001393769.1:c.5647A>GClinVar 2410972 rs771092834

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
2410972	Likely benign	criteria provided, single submitter	1	Inborn genetic diseases; Acute myeloid leukemia	germline	2	Apr 25, 2022	clinvar