List of variants in gene APRT reported as likely benign for inborn disorder of amino acid metabolism

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000485.3(APRT):c.162C>T (p.His54=)	rs145490332	0.00298
NM_000485.3(APRT):c.459C>T (p.Cys153=)	rs375131814	0.00004
NM_000485.3(APRT):c.385C>T (p.Leu129=)	rs376129456	0.00001
NM_000485.3(APRT):c.*178A>C	rs4695
NM_000485.3(APRT):c.400+14C>T	rs373048958

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