"Ambry Genetics"[submitter] AND "ZBTB34"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2267464	NM_001099270.4(ZBTB34):c.416A>C (p.Asp139Ala)	ZBTB34 (D139A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591209	NM_001099270.4(ZBTB34):c.479T>C (p.Phe160Ser)	ZBTB34 (F160S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2224196	NM_001099270.4(ZBTB34):c.526C>T (p.Arg176Trp)	ZBTB34 (R176W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192015	NM_001099270.4(ZBTB34):c.563C>T (p.Thr188Met)	ZBTB34 (T198M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325197	NM_001099270.4(ZBTB34):c.593T>C (p.Leu198Ser)	ZBTB34 (L208S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340612	NM_001099270.4(ZBTB34):c.821T>C (p.Val274Ala)	ZBTB34 (V284A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398210	NM_001099270.4(ZBTB34):c.886C>T (p.Pro296Ser)	ZBTB34 (P296S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329576	NM_001099270.4(ZBTB34):c.967C>T (p.Arg323Cys)	ZBTB34 (R323C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192016	NM_001099270.4(ZBTB34):c.968G>A (p.Arg323His)	ZBTB34 (R323H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192017	NM_001099270.4(ZBTB34):c.970G>T (p.Ala324Ser)	ZBTB34 (A324S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192018	NM_001099270.4(ZBTB34):c.974G>A (p.Arg325His)	ZBTB34 (R325H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192008	NM_001099270.4(ZBTB34):c.1042G>A (p.Glu348Lys)	ZBTB34 (E348K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192009	NM_001099270.4(ZBTB34):c.1060C>T (p.Pro354Ser)	ZBTB34 (P354S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532740	NM_001099270.4(ZBTB34):c.1087A>G (p.Arg363Gly)	ZBTB34 (R373G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192010	NM_001099270.4(ZBTB34):c.1088G>A (p.Arg363Lys)	ZBTB34 (R363K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480318	NM_001099270.4(ZBTB34):c.1090A>C (p.Ser364Arg)	ZBTB34 (S364R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216394	NM_001099270.4(ZBTB34):c.1094C>G (p.Ala365Gly)	ZBTB34 (A365G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192012	NM_001099270.4(ZBTB34):c.1112C>A (p.Pro371Gln)	ZBTB34 (P381Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617325	NM_001099270.4(ZBTB34):c.1180C>T (p.His394Tyr)	ZBTB34 (H394Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2247039	NM_001099270.4(ZBTB34):c.1208C>A (p.Pro403His)	ZBTB34 (P403H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312652	NM_001099270.4(ZBTB34):c.1211T>A (p.Phe404Tyr)	ZBTB34 (F404Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333914	NM_001099270.4(ZBTB34):c.1250A>T (p.Asp417Val)	ZBTB34 (D417V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3333915	NM_001099270.4(ZBTB34):c.1393A>G (p.Ile465Val)	ZBTB34 (I475V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192013	NM_001099270.4(ZBTB34):c.1423G>A (p.Val475Met)	ZBTB34 (V485M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3192014	NM_001099270.4(ZBTB34):c.1484A>G (p.Glu495Gly)	ZBTB34 (E495G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 25