FOXO4[gene] and "single gene"[properties] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 24

	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 3279653	NM_005938.4(FOXO4):c.43A>T (p.Ile15Phe)	FOXO4 (I15F)	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 993788	NM_005938.4(FOXO4):c.385G>T (p.Glu129Ter)	FOXO4 (E129* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2570667	NM_005938.4(FOXO4):c.449G>A (p.Trp150Ter)	FOXO4 (W95* +1 more)	Single nucleotide variant (nonsense)	Clinodactyly +4 more	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 2660837	NM_005938.4(FOXO4):c.666A>C (p.Pro222=)	FOXO4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 788055	NM_005938.4(FOXO4):c.687G>A (p.Thr229=)	FOXO4	Single nucleotide variant (synonymous variant)	not provided	GBenign
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 1334901	NM_005938.4(FOXO4):c.830A>C (p.Glu277Ala)	FOXO4 (E222A +1 more)	Single nucleotide variant (missense variant)	Intellectual disability	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 2660838	NM_005938.4(FOXO4):c.1140C>T (p.Asp380=)	FOXO4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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
Select item 3279655	NM_005938.4(FOXO4):c.1420A>G (p.Met474Val)	FOXO4 (M419V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 24