Related gene-specific medical variations for Gene (Select 56832) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2603485	NM_020124.3(IFNK):c.20T>C (p.Met7Thr)	IFNK, MOB3B (M7T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402508	NM_020124.3(IFNK):c.163T>C (p.Phe55Leu)	IFNK, MOB3B (F55L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401734	NM_020124.3(IFNK):c.347T>C (p.Ile116Thr)	IFNK, MOB3B (I116T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2395236	NM_020124.3(IFNK):c.134T>C (p.Leu45Pro)	IFNK, MOB3B (L45P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2314668	NM_020124.3(IFNK):c.102C>G (p.Asn34Lys)	IFNK, MOB3B (N34K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2294412	NM_020124.3(IFNK):c.179T>C (p.Leu60Pro)	IFNK, MOB3B (L60P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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