Related gene-specific medical variations for Gene (Select 1847) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2590716	NM_004419.4(DUSP5):c.112A>T (p.Asn38Tyr)	DUSP5, LOC130004716 (N38Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545352	NM_004419.4(DUSP5):c.280C>T (p.Arg94Cys)	DUSP5, LOC130004717 (R94C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481030	NM_004419.4(DUSP5):c.88C>T (p.Pro30Ser)	DUSP5, LOC130004716 (P30S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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