"PreventionGenetics, part of Exact Sciences"[submitter] AND "NPM1"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3033346	NM_002520.7(NPM1):c.39G>A (p.Arg13=)	NPM1	Single nucleotide variant (synonymous variant +2 more)	NPM1-related disorder	GLikely benign
Select item 3057493	NM_002520.7(NPM1):c.177T>C (p.Ile59=)	NPM1	Single nucleotide variant (synonymous variant +3 more)	NPM1-related disorder	GLikely benign
Select item 730555	NM_002520.7(NPM1):c.495C>T (p.Asp165=)	NPM1	Single nucleotide variant (synonymous variant)	NPM1-related disorder +1 more	GBenign
Select item 2631984	NM_002520.7(NPM1):c.513TGA[2] (p.Asp173del)	NPM1 (D109del +2 more)	Microsatellite (inframe_deletion +1 more)	NPM1-related disorder	GUncertain significance
Select item 3057997	NM_002520.7(NPM1):c.847-6_847-5dup	NPM1	Duplication (intron variant)	NPM1-related disorder	GLikely benign
Select item 3045006	NM_002520.7(NPM1):c.847-6_847-5del	NPM1	Deletion (intron variant)	NPM1-related disorder	GBenign

ClinVar