"Ambry Genetics"[submitter] AND "FOXO4"[gene] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2359238	NM_005938.4(FOXO4):c.11G>T (p.Gly4Val)	FOXO4 (G4V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096554	NM_005938.4(FOXO4):c.197C>G (p.Pro66Arg)	FOXO4 (P66R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2473156	NM_005938.4(FOXO4):c.248G>A (p.Gly83Glu)	FOXO4 (G83E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2406423	NM_005938.4(FOXO4):c.508G>A (p.Glu170Lys)	FOXO4 (E170K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207409	NM_005938.4(FOXO4):c.560G>C (p.Ser187Thr)	FOXO4 (S132T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367140	NM_005938.4(FOXO4):c.644A>G (p.Lys215Arg)	FOXO4 (K215R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519080	NM_005938.4(FOXO4):c.670G>A (p.Glu224Lys)	FOXO4 (E224K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2397025	NM_005938.4(FOXO4):c.686C>T (p.Thr229Met)	FOXO4 (T229M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2524139	NM_005938.4(FOXO4):c.697G>A (p.Gly233Ser)	FOXO4 (G178S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536689	NM_005938.4(FOXO4):c.946C>T (p.His316Tyr)	FOXO4 (H316Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096556	NM_005938.4(FOXO4):c.950C>T (p.Ser317Phe)	FOXO4 (S262F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2490462	NM_005938.4(FOXO4):c.1136C>T (p.Ala379Val)	FOXO4, LOC130068408 (A379V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511932	NM_005938.4(FOXO4):c.1151C>A (p.Thr384Asn)	FOXO4 (T384N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2353985	NM_005938.4(FOXO4):c.1234G>A (p.Val412Ile)	FOXO4 (V357I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096552	NM_005938.4(FOXO4):c.1268G>A (p.Gly423Asp)	FOXO4 (G368D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096553	NM_005938.4(FOXO4):c.1334T>C (p.Ile445Thr)	FOXO4 (I390T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213979	NM_005938.4(FOXO4):c.1357G>A (p.Val453Met)	FOXO4 (V453M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance