C0025221[trait identifier] AND "Dermatology, The Second Affiliated Hos - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 4602	NM_020427.3(SLURP1):c.256G>A (p.Gly86Arg)	SLURP1 (G86R)	Single nucleotide variant (missense variant)	not provided	GPathogenic
Select item 2504644	NM_020427.3(SLURP1):c.243C>A (p.Asp81Glu)	SLURP1 (D81E)	Single nucleotide variant (missense variant)	Acroerythrokeratoderma	GPathogenic
Select item 2500803	NM_020427.3(SLURP1):c.211C>T (p.Arg71Cys)	SLURP1 (R71C)	Single nucleotide variant (missense variant)	Acroerythrokeratoderma	GPathogenic

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