HNF4A NM_175914.5(HNF4A):c.358T>C (p.Ser120Pro)

CI-VAR-00134588Explore in graph →p.Ser120ProNM_175914.5:c.358T>CClinVar 804915 rs780342162

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
804915	Uncertain significance/Uncertain risk allele	criteria provided, multiple submitters, no conflicts	2	Maturity-onset diabetes of the young; Fanconi renotubular syndrome 4 with maturity-onset diabetes of the young; Maturity-onset diabetes of the young type 1; Type 2 diabetes mellitus	germline	4	May 13, 2025	clinvar