ClinVar for Gene (Select 2308) - ClinVar

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Links from Gene

Items: 95

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3337125	NM_002015.4(FOXO1):c.800G>A (p.Arg267Gln)	FOXO1 (R267Q)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3279644	NM_002015.4(FOXO1):c.1531G>T (p.Ala511Ser)	FOXO1 (A511S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279643	NM_002015.4(FOXO1):c.275C>T (p.Ala92Val)	FOXO1, LOC130009610 (A92V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279642	NM_002015.4(FOXO1):c.1342A>G (p.Ser448Gly)	FOXO1 (S448G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279641	NM_002015.4(FOXO1):c.1199A>T (p.Gln400Leu)	FOXO1 (Q400L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279640	NM_002015.4(FOXO1):c.1741G>A (p.Val581Met)	FOXO1 (V581M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3279639	NM_002015.4(FOXO1):c.1618C>T (p.Pro540Ser)	FOXO1 (P540S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3279638	NM_002015.4(FOXO1):c.95T>A (p.Phe32Tyr)	FOXO1 (F32Y)	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 3096543	NM_002015.4(FOXO1):c.1781A>G (p.His594Arg)	FOXO1 (H594R)	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 3096541	NM_002015.4(FOXO1):c.1486G>A (p.Val496Ile)	FOXO1 (V496I)	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 3096538	NM_002015.4(FOXO1):c.1066G>A (p.Ala356Thr)	FOXO1 (A356T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3063311	GRCh37/hg19 13q13.2-21.1(chr13:35015723-59553519)x3	AKAP11, ALG11 +117 more	Copy number gain	not specified	GPathogenic
Select item 3063306	GRCh37/hg19 13q13.2-14.11(chr13:35060982-44540846)x1	AKAP11, ALG5 +42 more	Copy number loss	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 3024581	GRCh37/hg19 13q13.2-21.2(chr13:34884647-61309742)x1	ITM2B, KBTBD6 +119 more	Copy number loss	not provided	GPathogenic
Select item 2685055	GRCh37/hg19 13q14.11(chr13:41203615-41527048)x4	ELF1, FOXO1 +2 more	Copy number gain	not provided	GUncertain significance
Select item 2643778	NM_002015.4(FOXO1):c.54C>T (p.Pro18=)	FOXO1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2643777	NM_002015.4(FOXO1):c.378G>C (p.Pro126=)	FOXO1, LOC130009609	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
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 2607915	NM_002015.4(FOXO1):c.1579C>T (p.His527Tyr)	FOXO1 (H527Y)	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 2574035	NM_002015.4(FOXO1):c.482G>A (p.Gly161Asp)	FOXO1 (G161D)	Single nucleotide variant	Malignant lymphoma, large B-cell, diffuse	GPathogenic
Select item 2548335	NM_002015.4(FOXO1):c.1346A>G (p.Tyr449Cys)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529933	NM_002015.4(FOXO1):c.1878T>A (p.Asp626Glu)	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 2487884	NM_002015.4(FOXO1):c.764C>T (p.Ala255Val)	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 2480669	NM_002015.4(FOXO1):c.268G>C (p.Val90Leu)	FOXO1, LOC130009610	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409222	NM_002015.4(FOXO1):c.965G>C (p.Ser322Thr)	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 2389394	NM_002015.4(FOXO1):c.1414C>T (p.Pro472Ser)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2384696	NM_002015.4(FOXO1):c.269T>G (p.Val90Gly)	FOXO1, LOC130009610	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 2358877	NM_002015.4(FOXO1):c.307A>C (p.Thr103Pro)	FOXO1	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 2304591	NM_002015.4(FOXO1):c.464C>G (p.Ser155Cys)	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 2283174	NM_002015.4(FOXO1):c.98G>C (p.Ser33Thr)	FOXO1	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 2269602	NM_002015.4(FOXO1):c.1468C>T (p.Arg490Trp)	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 2233913	NM_002015.4(FOXO1):c.334G>T (p.Gly112Cys)	FOXO1	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227850	NM_002015.4(FOXO1):c.413C>T (p.Pro138Leu)	FOXO1, LOC130009609	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2209509	NM_002015.4(FOXO1):c.281T>G (p.Val94Gly)	FOXO1, LOC130009610	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808770	GRCh37/hg19 13q13.3-14.11(chr13:36148057-41670428)x3	ALG5, CCDC169 +26 more	Copy number gain	not provided	GUncertain significance
Select item 1710518	GRCh37/hg19 13q11-34(chr13:19253848-115108937)x3	B3GLCT, HS6ST3 +332 more	Copy number gain	not provided	GPathogenic
Select item 1703573	GRCh37/hg19 13p13-q34(chr13:1-115169878)	ABCC4, ABHD13 +332 more	Copy number gain	Complete trisomy 13 syndrome	GPathogenic
Select item 1527767	GRCh37/hg19 13q13.3-14.11(chr13:39428367-43608103)	AKAP11, COG6 +21 more	Copy number loss	not specified	GUncertain significance
Select item 1527766	GRCh37/hg19 13q13.3-31.1(chr13:36376204-80681753)	SPART, SPRYD7 +147 more	Copy number loss	not specified	GPathogenic
Select item 1527762	GRCh37/hg19 13q13.1-21.31(chr13:32946120-62698217)	AKAP11, ALG11 +127 more	Copy number loss	not specified	GPathogenic
Select item 1527750	GRCh37/hg19 13q11-34(chr13:19436286-115107733)	ABCC4, ABHD13 +332 more	Copy number gain	not specified	GPathogenic
Select item 1527749	GRCh37/hg19 13q11-34(chr13:19436286-114981726)	VPS36, VWA8 +329 more	Copy number gain	not specified	GPathogenic
Select item 1341081	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 1321996	GRCh37/hg19 13p13-q34(chr13:1-115169878)x3	DACH1, IRS2 +332 more	Copy number gain	See cases	GPathogenic
Select item 1291640	NM_002015.4(FOXO1):c.*1254G>A	FOXO1	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1048617	GRCh37/hg19 13q11-34(chr13:19053605-115108528)x3	CENPJ, CHAMP1 +332 more	Copy number gain	See cases	GPathogenic
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 786748	NM_002015.4(FOXO1):c.1506G>A (p.Ser502=)	FOXO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 708958	NM_002015.4(FOXO1):c.921T>C (p.Phe307=)	FOXO1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 688438	GRCh37/hg19 13q11-34(chr13:19436286-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	not provided	GPathogenic
Select item 564083	GRCh37/hg19 13q11-22.1(chr13:19436286-74045459)x3	NUDT15, NUFIP1 +211 more	Copy number gain	not provided	GPathogenic
Select item 564024	GRCh37/hg19 13q14.11(chr13:41202702-41506651)x4	ELF1, MRPS31 +2 more	Copy number gain	not provided	GUncertain significance
Select item 441765	GRCh37/hg19 13q11-34(chr13:19436287-115107733)	FGF9, FLT1 +332 more	Copy number gain	See cases	GPathogenic
Select item 441764	GRCh37/hg19 13q11-34(chr13:19436287-115107733)x3	ABCC4, ABHD13 +332 more	Copy number gain	See cases	GPathogenic
Select item 394462	GRCh37/hg19 13q12.11-34(chr13:19571503-115092510)	CRYL1, CSNK1A1L +332 more	Copy number gain	See cases	GPathogenic
Select item 253405	GRCh37/hg19 13q12.11-34(chr13:19571503-115092569)x3	GTF2F2, LINC00567 +332 more	Copy number gain	See cases	GPathogenic
Select item 161028	GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3	ACOD1, AKAP11 +992 more	Copy number gain	See cases	GPathogenic
Select item 160881	GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	LOC126861859, LOC126861860 +2025 more	Copy number gain	See cases	GPathogenic
Select item 155395	GRCh38/hg38 13q11-34(chr13:18862146-114342258)x3	ABCC4, ABHD13 +2046 more	Copy number gain	See cases	GPathogenic
Select item 154857	GRCh38/hg38 13q12.11-34(chr13:19671934-114340331)x3	LOC130009607, LOC130009608 +2029 more	Copy number gain	See cases	GPathogenic
Select item 154825	GRCh38/hg38 13q14.11(chr13:39860568-43580405)x3	LOC130009641, LOC130009642 +141 more	Copy number gain	See cases	GUncertain significance
Select item 152159	GRCh38/hg38 13q13.3-14.3(chr13:38514177-51425214)x1	LOC126861769, LOC126861770 +437 more	Copy number loss	See cases	GPathogenic
Select item 152095	GRCh38/hg38 13q13.3-21.32(chr13:37864226-67963788)x1	LOC130009665, LOC130009659 +612 more	Copy number loss	See cases	GPathogenic
Select item 151282	GRCh38/hg38 13q11-34(chr13:18456040-114340285)x3	LOC130009892, LOC130009893 +2050 more	Copy number gain	See cases	GPathogenic
Select item 150189	GRCh38/hg38 13q12.11-34(chr13:19833130-114327106)x3	ABCC4, ABHD13 +2025 more	Copy number gain	See cases	GPathogenic
Select item 149761	GRCh38/hg38 13q12.3-14.2(chr13:31018160-48491204)x1	AKAP11, ALG5 +485 more	Copy number loss	See cases	GPathogenic
Select item 149289	GRCh38/hg38 13q13.1-31.1(chr13:32531486-86757044)x3	LOC130009611, LOC130009612 +938 more	Copy number gain	See cases	GPathogenic
Select item 148827	GRCh38/hg38 13q12.11-14.11(chr13:19671934-40914767)x3	LOC132090185, LOC132090186 +621 more	Copy number gain	See cases	GPathogenic
Select item 146536	GRCh38/hg38 13q12.3-21.32(chr13:31553608-65470367)x3	LOC130009600, LOC130009601 +735 more	Copy number gain	See cases	GPathogenic
Select item 146305	GRCh38/hg38 13q11-34(chr13:18445862-114327173)x1	ATP8A2, ATXN8OS +2049 more	Copy number loss	See cases	GPathogenic
Select item 144647	GRCh38/hg38 13q12.11-34(chr13:19833130-114298614)x3	LOC130009383, LOC130009384 +2022 more	Copy number gain	See cases	GPathogenic
Select item 144214	GRCh38/hg38 13q13.3-21.31(chr13:36777318-62955876)x1	LINC00400, LINC02333 +604 more	Copy number loss	See cases	GPathogenic
Select item 59888	GRCh38/hg38 13q13.2-34(chr13:33528097-114327173)x3	LOC130009687, LOC130009688 +1557 more	Copy number gain	See cases	GPathogenic
Select item 59868	GRCh38/hg38 13q12.3-31.1(chr13:30318913-83610426)x3	LOC130009567, LOC130009568 +1005 more	Copy number gain	See cases	GPathogenic
Select item 59863	GRCh38/hg38 13q12.11-34(chr13:19837395-114327173)x3	LOC112163664, LOC112163665 +2025 more	Copy number gain	See cases	GPathogenic
Select item 59858	GRCh38/hg38 13q12.11-34(chr13:18946182-114304628)x3	LOC130009309, LOC130009310 +2041 more	Copy number gain	See cases	GPathogenic
Select item 59855	GRCh38/hg38 13q11-34(chr13:18850545-114327173)x3	ABCC4, ABHD13 +2045 more	Copy number gain	See cases	GPathogenic
Select item 59851	GRCh38/hg38 13q11-34(chr13:18565048-114327173)x3	LOC130009819, LOC130009820 +2048 more	Copy number gain	See cases	GPathogenic
Select item 57640	GRCh38/hg38 13q13.3-14.11(chr13:35232476-41375955)x1	ALG5, CCDC169 +146 more	Copy number loss	See cases	GPathogenic
Select item 57638	GRCh38/hg38 13q12.3-21.33(chr13:30697728-69471973)x1	LOC130009620, LOC130009621 +781 more	Copy number loss	See cases	GPathogenic
Select item 33174	GRCh38/hg38 13q12.3-31.3(chr13:31363472-90575292)x3	ACOD1, AKAP11 +992 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 95