ClinVar for Gene (Select 27086) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3378126	NM_001349338.3(FOXP1):c.-168+2T>G	FOXP1	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 3377681	NM_001349338.3(FOXP1):c.775G>C (p.Val259Leu)	FOXP1 (V158L +4 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GUncertain significance
Select item 3376315	NM_001349338.3(FOXP1):c.1547del (p.Asn516fs)	FOXP1 (N415fs +4 more)	Deletion (frameshift variant +2 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GLikely pathogenic
Select item 3375679	NM_001349338.3(FOXP1):c.201G>C (p.Gln67His)	FOXP1 (Q67H)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3375536	NM_001349338.3(FOXP1):c.56G>C (p.Gly19Ala)	FOXP1 (G19A)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3372028	NM_001349338.3(FOXP1):c.1239_1241del (p.Leu414del)	FOXP1 (L313del +4 more)	Deletion (non-coding transcript variant)	not provided	GUncertain significance
Select item 3370498	NM_001349338.3(FOXP1):c.1590del (p.Ala532fs)	FOXP1 (A431fs +4 more)	Deletion (frameshift variant +2 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GPathogenic
Select item 3369273	NM_001349338.3(FOXP1):c.221A>C (p.Gln74Pro)	FOXP1 (Q74P)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 3366978	NM_001349338.3(FOXP1):c.1567T>C (p.Phe523Leu)	FOXP1 (F422L +4 more)	Single nucleotide variant (missense variant +2 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GLikely pathogenic
Select item 3365613	NM_001349338.3(FOXP1):c.670A>G (p.Ile224Val)	FOXP1 (I123V +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3363684	NM_001349338.3(FOXP1):c.861A>T (p.Lys287Asn)	FOXP1 (K186N +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3363651	NM_001349338.3(FOXP1):c.1035G>A (p.Met345Ile)	FOXP1 (M244I +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3363580	NM_001349338.3(FOXP1):c.712G>A (p.Ala238Thr)	FOXP1 (A137T +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3362144	NM_001349338.3(FOXP1):c.1026A>T (p.Arg342Ser)	FOXP1 (R241S +4 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3360952	NM_001349338.3(FOXP1):c.1640_1652+22dup	FOXP1	Duplication (splice donor variant +1 more)	not provided	GUncertain significance
Select item 3348433	NM_001349338.3(FOXP1):c.766A>G (p.Thr256Ala)	FOXP1 (T155A +4 more)	Single nucleotide variant (missense variant +1 more)	FOXP1-related disorder	GUncertain significance
Select item 3345807	NM_001349338.3(FOXP1):c.421-9C>A	FOXP1	Single nucleotide variant (intron variant)	FOXP1-related disorder	GLikely benign
Select item 3342346	NM_001349338.3(FOXP1):c.938G>A (p.Cys313Tyr)	FOXP1 (C212Y +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3340548	NM_001349338.3(FOXP1):c.1661C>T (p.Ser554Phe)	FOXP1 (S453F +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3337126	NM_001349338.3(FOXP1):c.1889+5G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely pathogenic
Select item 3336496	NM_001349338.3(FOXP1):c.510+10A>G	FOXP1	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 3279659	NM_001349338.3(FOXP1):c.1396CCA[1] (p.Pro467del)	FOXP1 (P366del +4 more)	Microsatellite (inframe_deletion +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3279658	NM_001349338.3(FOXP1):c.112A>G (p.Asn38Asp)	FOXP1 (N38D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3279657	NM_001349338.3(FOXP1):c.1616T>A (p.Val539Glu)	FOXP1 (V439E +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3279656	NM_001349338.3(FOXP1):c.1615G>C (p.Val539Leu)	FOXP1 (V439L +4 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3256796	NM_001349338.3(FOXP1):c.1397C>T (p.Pro466Leu)	FOXP1 (P365L +4 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GLikely pathogenic
Select item 3254669	NM_001349338.3(FOXP1):c.1433T>G (p.Ile478Ser)	FOXP1, LOC126806714 (I377S +4 more)	Single nucleotide variant (missense variant +1 more)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GLikely pathogenic
Select item 3252141	NM_001349338.3(FOXP1):c.1772G>C (p.Gly591Ala)	FOXP1 (G490A +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3251149	NM_001349338.3(FOXP1):c.1652+489C>G	FOXP1 (R549G)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3247053	NC_000003.11:g.(?_71008398)_(71247532_?)dup	FOXP1	Duplication	not provided	GUncertain significance
Select item 3247052	NC_000003.11:g.(?_71190318)_(71288982_?)del	FOXP1	Deletion	not provided	GPathogenic
Select item 3096561	NM_001349338.3(FOXP1):c.22G>C (p.Glu8Gln)	FOXP1 (E8Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3096559	NM_001349338.3(FOXP1):c.227A>G (p.Gln76Arg)	FOXP1 (Q76R)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 3096558	NM_001349338.3(FOXP1):c.1731G>A (p.Met577Ile)	FOXP1 (M593I +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3096557	NM_001349338.3(FOXP1):c.1656C>A (p.Asn552Lys)	FOXP1 (N476K +5 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3067830	NM_001349338.3(FOXP1):c.-11-36045A>C	FOXP1	Single nucleotide variant (intron variant)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GUncertain significance
Select item 3064883	NM_001349338.3(FOXP1):c.282+16777A>G	FOXP1	Single nucleotide variant (intron variant)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GUncertain significance
Select item 3062726	GRCh37/hg19 3p13(chr3:71469844-71622449)x1	FOXP1, FOXP1-IT1	Copy number loss	not specified	GPathogenic
Select item 3062713	GRCh37/hg19 3p14.2-13(chr3:62188399-71663248)x1	ADAMTS9, ARL6IP5 +24 more	Copy number loss	not specified	GPathogenic
Select item 3062672	GRCh37/hg19 3p13(chr3:70583776-72793789)x1	EIF4E3, FOXP1 +4 more	Copy number loss	not specified	GPathogenic
Select item 3061739	NM_001349338.3(FOXP1):c.1407A>G (p.Thr469=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3061505	NM_001349338.3(FOXP1):c.90C>G (p.Gly30=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3061436	NM_001349338.3(FOXP1):c.181-18007C>G	FOXP1 (H14D)	Single nucleotide variant (missense variant +1 more)	FOXP1-related disorder	GUncertain significance
Select item 3056315	NM_001349338.3(FOXP1):c.1652+350_1652+367del	FOXP1	Deletion (intron variant)	FOXP1-related disorder	GLikely benign
Select item 3052264	NM_001349338.3(FOXP1):c.181-17892G>A	FOXP1	Single nucleotide variant (5 prime UTR variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3051678	NM_001349338.3(FOXP1):c.1488A>T (p.Thr496=)	FOXP1, LOC126806714	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3049664	NM_001349338.3(FOXP1):c.180+209T>C	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3045160	NM_001349338.3(FOXP1):c.181-17966G>A	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3044278	NM_001349338.3(FOXP1):c.1652+380C>G	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3033991	NM_001349338.3(FOXP1):c.181-17970A>G	FOXP1 (H26R)	Single nucleotide variant (missense variant +1 more)	FOXP1-related disorder	GBenign
Select item 3029387	NM_001349338.3(FOXP1):c.1887C>T (p.Ala629=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	FOXP1-related disorder	GLikely benign
Select item 3028945	NM_001349338.3(FOXP1):c.787G>C (p.Ala263Pro)	FOXP1 (A162P +4 more)	Single nucleotide variant (missense variant +1 more)	FOXP1-related disorder	GUncertain significance
Select item 3026929	NM_001349338.3(FOXP1):c.180+212G>A	FOXP1 (E87K)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3024380	GRCh38/hg38 3p13(chr3:71518345-71562911)	FOXP1, LOC110121007 +1 more	Copy number loss	Autism spectrum disorder	GUncertain significance
Select item 3024288	NM_001349338.3(FOXP1):c.1429-3C>G	FOXP1, LOC126806714	Single nucleotide variant (intron variant)	Intellectual disability-severe speech delay-mild dysmorphism syndrome	GUncertain significance
Select item 3021448	NM_001349338.3(FOXP1):c.180+18C>G	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3021183	NM_001349338.3(FOXP1):c.511-12G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3016250	NM_001349338.3(FOXP1):c.1584C>T (p.Asn528=)	FOXP1	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 3011658	NM_001349338.3(FOXP1):c.1188G>A (p.Ser396=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3010588	NM_001349338.3(FOXP1):c.1653-17A>G	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3009756	NM_001349338.3(FOXP1):c.87C>T (p.Cys29=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3009313	NM_001349338.3(FOXP1):c.1858A>G (p.Ser620Gly)	FOXP1 (S520G +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3008989	NM_001349338.3(FOXP1):c.139G>A (p.Gly47Arg)	FOXP1 (G47R)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3008811	NM_001349338.3(FOXP1):c.1293G>A (p.Thr431=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3008797	NM_001349338.3(FOXP1):c.1975C>G (p.Pro659Ala)	FOXP1 (P658A +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 3007216	NM_001349338.3(FOXP1):c.909T>C (p.Tyr303=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3006974	NM_001349338.3(FOXP1):c.786T>C (p.Ser262=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3006690	NM_001349338.3(FOXP1):c.1890-10T>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 3001759	NM_001349338.3(FOXP1):c.172C>G (p.Gln58Glu)	FOXP1 (Q58E)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2999453	NM_001349338.3(FOXP1):c.181-14G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2995742	NM_001349338.3(FOXP1):c.1307G>A (p.Arg436His)	FOXP1 (R360H +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2995007	NM_001349338.3(FOXP1):c.1429-26_1429-12del	FOXP1, LOC126806714	Deletion (intron variant)	not provided	GUncertain significance
Select item 2994088	NM_001349338.3(FOXP1):c.996G>A (p.Ala332=)	FOXP1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2992961	NM_001349338.3(FOXP1):c.1104C>T (p.His368=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2990772	NM_001349338.3(FOXP1):c.870-14G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2989815	NM_001349338.3(FOXP1):c.1081C>T (p.Arg361Cys)	FOXP1 (R261C +4 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2989447	NM_001349338.3(FOXP1):c.1921G>A (p.Asp641Asn)	FOXP1 (D540N +5 more)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance
Select item 2989185	NM_001349338.3(FOXP1):c.1146+13C>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2988794	NM_001349338.3(FOXP1):c.181-16T>C	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2987997	NM_001349338.3(FOXP1):c.1158A>G (p.Val386=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2985470	NM_001349338.3(FOXP1):c.615G>C (p.Leu205=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2984080	NM_001349338.3(FOXP1):c.1152T>C (p.Asn384=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2983482	NM_001349338.3(FOXP1):c.1653-17A>C	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2983043	NM_001349338.3(FOXP1):c.338A>C (p.Gln113Pro)	FOXP1 (Q113P +1 more)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 2981403	NM_001349338.3(FOXP1):c.1147-9T>C	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2980733	NM_001349338.3(FOXP1):c.1429-20T>C	FOXP1, LOC126806714	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978815	NM_001349338.3(FOXP1):c.665-17C>T	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2978239	NM_001349338.3(FOXP1):c.1398A>G (p.Pro466=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2978095	NM_001349338.3(FOXP1):c.1524G>A (p.Thr508=)	FOXP1, LOC126806714	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2977909	NM_001349338.3(FOXP1):c.1530+13A>G	FOXP1, LOC126806714	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976841	NM_001349338.3(FOXP1):c.421-20G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2976840	NM_001349338.3(FOXP1):c.421-15C>T	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2973478	NM_001349338.3(FOXP1):c.1147-16_1147-14del	FOXP1	Microsatellite (intron variant)	not provided	GLikely benign
Select item 2971553	NM_001349338.3(FOXP1):c.1063-5G>A	FOXP1	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2969011	NM_001349338.3(FOXP1):c.129C>T (p.Ala43=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2968554	NM_001349338.3(FOXP1):c.1332C>T (p.Asn444=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2967884	NM_001349338.3(FOXP1):c.960C>T (p.Phe320=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2967248	NM_001349338.3(FOXP1):c.51G>A (p.Gln17=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2965455	NM_001349338.3(FOXP1):c.162C>T (p.Ala54=)	FOXP1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2964149	NM_001349338.3(FOXP1):c.300T>A (p.Ala100=)	FOXP1	Single nucleotide variant (synonymous variant +3 more)	not provided	GLikely benign

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