POMGNT1 NM_017739.4(POMGNT1):c.1489C>A (p.Arg497=)

CI-VAR-00271694Explore in graph →p.Arg497=NM_017739.4:c.1489C>AClinVar 2147219 rs745343484

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
2147219	Likely benign	criteria provided, single submitter	1	Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B3; Autosomal recessive limb-girdle muscular dystrophy type 2O; Papillary renal cell carcinoma type 1	germline	2	Feb 25, 2022	clinvar