"PreventionGenetics, part of Exact Sciences"[submitter] AND "PSMB9"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3044101	NM_002800.5(PSMB9):c.26G>A (p.Gly9Glu)	PSMB9 (G9E)	Single nucleotide variant (missense variant)	PSMB9-related disorder	GBenign
Select item 3056957	NM_002800.5(PSMB9):c.94G>A (p.Val32Ile)	PSMB9 (V32I)	Single nucleotide variant (missense variant)	PSMB9-related disorder	GBenign
Select item 1327454	NM_002800.5(PSMB9):c.179G>A (p.Arg60His)	PSMB9 (R60H)	Single nucleotide variant (missense variant)	not specified +2 more	GBenign
Select item 3037411	NM_002800.5(PSMB9):c.198T>C (p.Ser66=)	PSMB9	Single nucleotide variant (synonymous variant)	PSMB9-related disorder	GLikely benign
Select item 2637885	NM_002800.5(PSMB9):c.483A>G (p.Ala161=)	PSMB9	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 3043979	NM_002800.5(PSMB9):c.486T>C (p.Tyr162=)	PSMB9	Single nucleotide variant (synonymous variant)	PSMB9-related disorder	GBenign
Select item 1711625	NM_002800.5(PSMB9):c.517C>T (p.Arg173Cys)	PSMB9 (R173C)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 3046623	NM_002800.5(PSMB9):c.567C>T (p.Ser189=)	PSMB9	Single nucleotide variant (synonymous variant)	PSMB9-related disorder	GLikely benign

ClinVar