Related gene-specific medical variations for Gene (Select 9641) - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109015	NM_014002.4(IKBKE):c.2099A>G (p.Asn700Ser)	IKBKE, IKBKE-AS1 (N615S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109013	NM_014002.4(IKBKE):c.1919A>G (p.Glu640Gly)	IKBKE, IKBKE-AS1 (E555G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2624129	NM_014002.4(IKBKE):c.1953C>G (p.His651Gln)	IKBKE, IKBKE-AS1 (H651Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2542682	NM_014002.4(IKBKE):c.1988C>T (p.Ala663Val)	IKBKE, IKBKE-AS1 (A578V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2464290	NM_014002.4(IKBKE):c.1973C>T (p.Ala658Val)	IKBKE, IKBKE-AS1 (A573V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2331848	NM_014002.4(IKBKE):c.1897A>G (p.Thr633Ala)	IKBKE, IKBKE-AS1 (T548A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286992	NM_014002.4(IKBKE):c.2113G>C (p.Glu705Gln)	IKBKE, IKBKE-AS1 (E620Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254757	NM_014002.4(IKBKE):c.2000C>G (p.Pro667Arg)	IKBKE, IKBKE-AS1 (P582R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2243653	NM_014002.4(IKBKE):c.1952A>G (p.His651Arg)	IKBKE, IKBKE-AS1 (H566R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance