"Ambry Genetics"[submitter] AND "ENOX2"[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2308238	NM_006375.4(ENOX2):c.1739T>C (p.Leu580Pro)	ENOX2 (L578P +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2323977	NM_006375.4(ENOX2):c.1520T>G (p.Leu507Arg)	ENOX2 (L534R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558886	NM_006375.4(ENOX2):c.1474G>C (p.Glu492Gln)	ENOX2 (E521Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2507658	NM_006375.4(ENOX2):c.1465T>C (p.Tyr489His)	ENOX2 (Y489H +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275464	NM_006375.4(ENOX2):c.1441T>C (p.Cys481Arg)	ENOX2 (C510R +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212183	NM_006375.4(ENOX2):c.1433C>G (p.Ser478Cys)	ENOX2 (S476C +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275461	NM_006375.4(ENOX2):c.1231G>A (p.Gly411Ser)	ENOX2 (G409S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2554057	NM_006375.4(ENOX2):c.1037A>T (p.Asp346Val)	ENOX2 (D375V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617985	NM_006375.4(ENOX2):c.886C>G (p.Leu296Val)	ENOX2 (L325V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407017	NM_006375.4(ENOX2):c.818G>A (p.Arg273His)	ENOX2 (R365H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298900	NM_006375.4(ENOX2):c.743A>G (p.Glu248Gly)	ENOX2 (E340G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2555008	NM_006375.4(ENOX2):c.640C>G (p.Pro214Ala)	ENOX2 (P214A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375693	NM_006375.4(ENOX2):c.623G>A (p.Arg208His)	ENOX2 (R208H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275462	NM_006375.4(ENOX2):c.621G>C (p.Leu207Phe)	ENOX2 (L207F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088940	NM_006375.4(ENOX2):c.569G>A (p.Arg190His)	ENOX2 (R190H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2375643	NM_006375.4(ENOX2):c.530A>G (p.Gln177Arg)	ENOX2 (Q206R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088939	NM_006375.4(ENOX2):c.416G>A (p.Arg139His)	ENOX2 (R139H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275463	NM_006375.4(ENOX2):c.386G>A (p.Arg129His)	ENOX2 (R129H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088938	NM_006375.4(ENOX2):c.313G>A (p.Gly105Ser)	ENOX2 (G105S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495655	NM_006375.4(ENOX2):c.232A>G (p.Thr78Ala)	ENOX2 (T107A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410093	NM_006375.4(ENOX2):c.169G>A (p.Val57Ile)	ENOX2 (V57I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088937	NM_006375.4(ENOX2):c.148A>G (p.Met50Val)	ENOX2 (M142V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376952	NM_006375.4(ENOX2):c.71G>C (p.Gly24Ala)	ENOX2 (G53A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3088936	NM_006375.4(ENOX2):c.-38-6023T>G	ENOX2 (F5L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 24