Related gene-specific medical variations for Gene (Select 5698) - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Format

Sort by

Choose Destination

Links from Gene

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2637886	NC_000006.12:g.32859588_32859589insAT	PSMB9	Insertion	not specified	GBenign
Select item 2637877	NC_000006.12:g.32857571T>C	PSMB9	Single nucleotide variant	not specified	GBenign
Select item 2637873	NC_000006.12:g.32858673T>C	PSMB9	Single nucleotide variant	not specified	GBenign
Select item 2575959	NM_002800.5(PSMB9):c.323A>C (p.Tyr108Ser)	PSMB9 (Y108S)	Single nucleotide variant (missense variant)	not provided	GUncertain significance

Format

Sort by

Choose Destination