Related gene-specific medical variations for Gene (Select 10098) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 687329	GRCh37/hg19 4q23(chr4:99513451-99603864)x3	TSPAN5	Copy number gain	not provided	GUncertain significance
Select item 686424	GRCh37/hg19 4q23(chr4:99521332-99600079)x3	TSPAN5	Copy number gain	not provided	GUncertain significance
Select item 161639	NM_005723.4(TSPAN5):c.268C>A (p.Leu90Ile)	TSPAN5 (L90I)	Single nucleotide variant (missense variant)	Malignant tumor of prostate	GUncertain significance

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