FOXO1[gene] and "single gene"[properties] - ClinVar

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

Search results

Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1291640	NM_002015.4(FOXO1):c.*1254G>A	FOXO1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 2529933	NM_002015.4(FOXO1):c.1878T>A (p.Asp626Glu)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096543	NM_002015.4(FOXO1):c.1781A>G (p.His594Arg)	FOXO1 (H594R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326259	NM_002015.4(FOXO1):c.1757G>A (p.Gly586Asp)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302625	NM_002015.4(FOXO1):c.1708A>G (p.Met570Val)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096542	NM_002015.4(FOXO1):c.1624A>G (p.Thr542Ala)	FOXO1 (T542A)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2607915	NM_002015.4(FOXO1):c.1579C>T (p.His527Tyr)	FOXO1 (H527Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270795	NM_002015.4(FOXO1):c.1574C>G (p.Pro525Arg)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511786	NM_002015.4(FOXO1):c.1537C>T (p.His513Tyr)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251574	NM_002015.4(FOXO1):c.1517C>T (p.Thr506Ile)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 786748	NM_002015.4(FOXO1):c.1506G>A (p.Ser502=)	FOXO1	Single nucleotide variant (synonymous variant)	FOXO1-related disorder +1 more	GBenign
Select item 3096541	NM_002015.4(FOXO1):c.1486G>A (p.Val496Ile)	FOXO1 (V496I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269602	NM_002015.4(FOXO1):c.1468C>T (p.Arg490Trp)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2389394	NM_002015.4(FOXO1):c.1414C>T (p.Pro472Ser)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2601224	NM_002015.4(FOXO1):c.1358G>A (p.Ser453Asn)	FOXO1 (S453N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2548335	NM_002015.4(FOXO1):c.1346A>G (p.Tyr449Cys)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096540	NM_002015.4(FOXO1):c.1181C>T (p.Ser394Leu)	FOXO1 (S394L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096539	NM_002015.4(FOXO1):c.1097G>A (p.Ser366Asn)	FOXO1 (S366N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2621486	NM_002015.4(FOXO1):c.1096A>G (p.Ser366Gly)	FOXO1 (S366G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096538	NM_002015.4(FOXO1):c.1066G>A (p.Ala356Thr)	FOXO1 (A356T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 791400	NM_002015.4(FOXO1):c.999C>T (p.Thr333=)	FOXO1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2409222	NM_002015.4(FOXO1):c.965G>C (p.Ser322Thr)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 708958	NM_002015.4(FOXO1):c.921T>C (p.Phe307=)	FOXO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 2487884	NM_002015.4(FOXO1):c.764C>T (p.Ala255Val)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2574035	NM_002015.4(FOXO1):c.482G>A (p.Gly161Asp)	FOXO1 (G161D)	Single nucleotide variant	Malignant lymphoma, large B-cell, diffuse	GPathogenic
Select item 2304591	NM_002015.4(FOXO1):c.464C>G (p.Ser155Cys)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371773	NM_002015.4(FOXO1):c.335G>T (p.Gly112Val)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233913	NM_002015.4(FOXO1):c.334G>T (p.Gly112Cys)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393108	NM_002015.4(FOXO1):c.319T>C (p.Cys107Arg)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3058373	NM_002015.4(FOXO1):c.311G>C (p.Gly104Ala)	FOXO1 (G104A)	Single nucleotide variant (missense variant)	FOXO1-related disorder	GLikely benign
Select item 2358877	NM_002015.4(FOXO1):c.307A>C (p.Thr103Pro)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483766	NM_002015.4(FOXO1):c.301G>A (p.Ala101Thr)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283174	NM_002015.4(FOXO1):c.98G>C (p.Ser33Thr)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3096545	NM_002015.4(FOXO1):c.94T>G (p.Phe32Val)	FOXO1 (F32V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643778	NM_002015.4(FOXO1):c.54C>T (p.Pro18=)	FOXO1	Single nucleotide variant (synonymous variant)	FOXO1-related disorder +1 more	GLikely benign

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: 35