{"query":"TP53(NM_000546):R175H","kind":"protein","recognisedAs":"Protein change","results":[{"kind":"variant","id":"17-7675088-C-T","route":"/variant/17-7675088-C-T/","label":"17-7675088-C-T","description":"NM_000546.6(TP53):c.524G>A (p.Arg175His) · Pathogenic","source":"ClinVar VCV000012374, dbNSFP via MyVariant.info"}]}