"Ambry Genetics"[submitter] AND "ZBTB44"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3192098	NM_001301098.2(ZBTB44):c.1229G>A (p.Arg410His)	ZBTB44 (R392H +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192097	NM_001301098.2(ZBTB44):c.1186G>A (p.Asp396Asn)	ZBTB44 (D396N +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2469425	NM_001301098.2(ZBTB44):c.1120T>C (p.Tyr374His)	ZBTB44 (Y374H)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3192096	NM_001301098.2(ZBTB44):c.1118A>G (p.Gln373Arg)	ZBTB44 (Q373R)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 3192095	NM_001301098.2(ZBTB44):c.1118A>C (p.Gln373Pro)	ZBTB44 (Q373P)	Single nucleotide variant (missense variant +3 more)	not specified	GUncertain significance
Select item 2553471	NM_001301098.2(ZBTB44):c.1004A>T (p.Gln335Leu)	ZBTB44 (Q335L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2610369	NM_001301098.2(ZBTB44):c.962C>T (p.Pro321Leu)	ZBTB44 (P321L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2355299	NM_001301098.2(ZBTB44):c.903G>T (p.Glu301Asp)	ZBTB44 (E301D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192106	NM_001301098.2(ZBTB44):c.899A>G (p.His300Arg)	ZBTB44 (H300R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192105	NM_001301098.2(ZBTB44):c.871G>A (p.Val291Ile)	ZBTB44 (V291I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2528325	NM_001301098.2(ZBTB44):c.808G>C (p.Val270Leu)	ZBTB44 (V270L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2355631	NM_001301098.2(ZBTB44):c.806A>T (p.Tyr269Phe)	ZBTB44 (Y269F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2207137	NM_001301098.2(ZBTB44):c.787G>T (p.Gly263Cys)	ZBTB44 (G263C)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2264284	NM_001301098.2(ZBTB44):c.757A>G (p.Thr253Ala)	ZBTB44 (T253A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2386461	NM_001301098.2(ZBTB44):c.748A>G (p.Asn250Asp)	ZBTB44 (N250D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192104	NM_001301098.2(ZBTB44):c.684T>G (p.Phe228Leu)	ZBTB44 (F228L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192103	NM_001301098.2(ZBTB44):c.608G>T (p.Ser203Ile)	ZBTB44 (S203I)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192102	NM_001301098.2(ZBTB44):c.569T>G (p.Met190Arg)	ZBTB44 (M190R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2376353	NM_001301098.2(ZBTB44):c.526G>C (p.Val176Leu)	ZBTB44 (V176L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192101	NM_001301098.2(ZBTB44):c.520A>G (p.Ile174Val)	ZBTB44 (I174V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2570200	NM_001301098.2(ZBTB44):c.498G>C (p.Glu166Asp)	ZBTB44 (E166D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192100	NM_001301098.2(ZBTB44):c.469G>A (p.Asp157Asn)	ZBTB44 (D157N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3192099	NM_001301098.2(ZBTB44):c.455A>G (p.Asn152Ser)	ZBTB44 (N152S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2322536	NM_001301098.2(ZBTB44):c.418G>C (p.Gly140Arg)	ZBTB44 (G140R)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3333958	NM_001301098.2(ZBTB44):c.188A>C (p.Gln63Pro)	ZBTB44 (Q63P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 25