Related gene-specific medical variations for Gene (Select 3836) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3116169	NM_002264.4(KPNA1):c.92A>G (p.Glu31Gly)	KPNA1, LOC126806788 (E31G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3116166	NM_002264.4(KPNA1):c.1022A>G (p.Gln341Arg)	KPNA1, WDR5B-DT (Q341R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2411068	NM_002264.4(KPNA1):c.1537A>G (p.Ile513Val)	KPNA1, WDR5B-DT (I513V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2336289	NM_002264.4(KPNA1):c.1426T>G (p.Tyr476Asp)	KPNA1, WDR5B-DT (Y476D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2265181	NM_002264.4(KPNA1):c.1258G>A (p.Val420Ile)	KPNA1, WDR5B-DT (V420I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 774847	NM_002264.4(KPNA1):c.1185G>A (p.Arg395=)	KPNA1, WDR5B-DT	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

ClinVar