"Ambry Genetics"[submitter] AND "IKZF2"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608418	NM_001387220.1(IKZF2):c.1523G>C (p.Ser508Thr)	IKZF2 (S433T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2547029	NM_001387220.1(IKZF2):c.1375A>G (p.Lys459Glu)	IKZF2 (K433E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2615997	NM_001387220.1(IKZF2):c.1330T>G (p.Leu444Val)	IKZF2 (L369V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109025	NM_001387220.1(IKZF2):c.1251C>G (p.His417Gln)	IKZF2 (H391Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307566	NM_001387220.1(IKZF2):c.1241A>C (p.His414Pro)	IKZF2 (H414P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305551	NM_001387220.1(IKZF2):c.1163G>A (p.Arg388Lys)	IKZF2 (R388K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109023	NM_001387220.1(IKZF2):c.1091T>C (p.Ile364Thr)	IKZF2 (I338T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285711	NM_001387220.1(IKZF2):c.1085A>G (p.Asn362Ser)	IKZF2 (N362S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612312	NM_001387220.1(IKZF2):c.954C>A (p.Asp318Glu)	IKZF2 (D318E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210552	NM_001387220.1(IKZF2):c.905A>G (p.Asn302Ser)	IKZF2 (N302S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285113	NM_001387220.1(IKZF2):c.796A>G (p.Ile266Val)	IKZF2 (I266V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2352140	NM_001387220.1(IKZF2):c.761A>G (p.Asn254Ser)	IKZF2 (N228S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109030	NM_001387220.1(IKZF2):c.742G>C (p.Glu248Gln)	IKZF2 (E222Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2507524	NM_001387220.1(IKZF2):c.731G>T (p.Cys244Phe)	IKZF2 (C218F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2299976	NM_001387220.1(IKZF2):c.719C>T (p.Pro240Leu)	IKZF2 (P214L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3109029	NM_001387220.1(IKZF2):c.661T>C (p.Tyr221His)	IKZF2 (Y195H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109028	NM_001387220.1(IKZF2):c.660C>G (p.Asn220Lys)	IKZF2 (N193K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237082	NM_001387220.1(IKZF2):c.457G>C (p.Gly153Arg)	IKZF2 (G153R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109026	NM_001387220.1(IKZF2):c.433T>C (p.Cys145Arg)	IKZF2 (C145R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285709	NM_001387220.1(IKZF2):c.412C>T (p.Arg138Cys)	IKZF2 (R112C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3285710	NM_001387220.1(IKZF2):c.329G>A (p.Gly110Asp)	IKZF2 (G110D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2495084	NM_001387220.1(IKZF2):c.260G>A (p.Ser87Asn)	IKZF2 (S86N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2276165	NM_001387220.1(IKZF2):c.225T>G (p.Asp75Glu)	IKZF2 (D74E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383769	NM_001387220.1(IKZF2):c.221A>T (p.His74Leu)	IKZF2 (H74L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622921	NM_001387220.1(IKZF2):c.197G>C (p.Ser66Thr)	IKZF2 (S65T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3109031	NM_001387220.1(IKZF2):c.80T>C (p.Ile27Thr)	IKZF2 (I27T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 26