"Ambry Genetics"[submitter] AND "LOC105369781"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3109045	NM_022465.4(IKZF4):c.28C>T (p.Arg10Cys)	IKZF4, LOC105369781 (R10C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3285717	NM_022465.4(IKZF4):c.43G>A (p.Gly15Ser)	IKZF4, LOC105369781 (G15S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2560850	NM_022465.4(IKZF4):c.53G>A (p.Arg18His)	IKZF4, LOC105369781 (R18H)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109048	NM_022465.4(IKZF4):c.59C>T (p.Pro20Leu)	IKZF4, LOC105369781 (P20L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109049	NM_022465.4(IKZF4):c.67C>T (p.His23Tyr)	IKZF4, LOC105369781 (H23Y)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3109050	NM_022465.4(IKZF4):c.70C>T (p.Arg24Trp)	IKZF4, LOC105369781 (R24W)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2281674	NM_022465.4(IKZF4):c.119C>T (p.Pro40Leu)	IKZF4, LOC105369781 (P40L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109044	NM_022465.4(IKZF4):c.149A>G (p.Asn50Ser)	IKZF4, LOC105369781 (N50S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar