Related gene-specific medical variations for Gene (Select 54059) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2392524	NM_058180.5(C21orf58):c.853A>G (p.Arg285Gly)	C21orf58, YBEY (R179G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224384	NM_058180.5(C21orf58):c.911C>T (p.Pro304Leu)	YBEY, C21orf58 (P304L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 402442	NM_058180.5(C21orf58):c.876CCA[8] (p.His299dup)	C21orf58, YBEY	Microsatellite (inframe_insertion)	not specified	GBenign

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