ClinVar Miner

List of variants in gene FOXP1 reported as uncertain significance for Intellectual Disability with Language Impairment and Autistic Features

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP
NM_032682.5(FOXP1):c.*1027_*1030dupCTTT rs886058851
NM_032682.5(FOXP1):c.*1037_*1040delCTTT rs886058850
NM_032682.5(FOXP1):c.*1037_*1041delCTTTT rs549654259
NM_032682.5(FOXP1):c.*1049_*1050dupTT rs747818299
NM_032682.5(FOXP1):c.*1100T>C rs886058848
NM_032682.5(FOXP1):c.*1104C>A rs886058847
NM_032682.5(FOXP1):c.*1131T>G rs867338460
NM_032682.5(FOXP1):c.*119A>G rs886058862
NM_032682.5(FOXP1):c.*1208C>T rs771846939
NM_032682.5(FOXP1):c.*1209G>A rs886058846
NM_032682.5(FOXP1):c.*1231_*1235dupTGTTT rs373349025
NM_032682.5(FOXP1):c.*1306G>A rs886058844
NM_032682.5(FOXP1):c.*1523G>T rs886058843
NM_032682.5(FOXP1):c.*1541dupG rs570372825
NM_032682.5(FOXP1):c.*1669dupT rs886058842
NM_032682.5(FOXP1):c.*1857A>G rs886058841
NM_032682.5(FOXP1):c.*2067A>G rs557236485
NM_032682.5(FOXP1):c.*2204_*2205delGA rs779139545
NM_032682.5(FOXP1):c.*2237G>A rs886058840
NM_032682.5(FOXP1):c.*2312T>C rs886058839
NM_032682.5(FOXP1):c.*2362A>G rs886058838
NM_032682.5(FOXP1):c.*2473T>A rs780171188
NM_032682.5(FOXP1):c.*2473_*2482delTAAAAAAAAA rs886058837
NM_032682.5(FOXP1):c.*2757dupA rs886058836
NM_032682.5(FOXP1):c.*2831dupA rs112098084
NM_032682.5(FOXP1):c.*2832delG rs886058835
NM_032682.5(FOXP1):c.*2837dupA rs886058834
NM_032682.5(FOXP1):c.*2979C>T rs886058833
NM_032682.5(FOXP1):c.*3192delA rs535202716
NM_032682.5(FOXP1):c.*3303dupC rs886058832
NM_032682.5(FOXP1):c.*3313T>C rs886058831
NM_032682.5(FOXP1):c.*3402G>A rs886058830
NM_032682.5(FOXP1):c.*3403delT rs886058829
NM_032682.5(FOXP1):c.*3407_*3414dupTGTGTGTG rs143202281
NM_032682.5(FOXP1):c.*3411_*3414delTGTG rs143202281
NM_032682.5(FOXP1):c.*3411_*3414dupTGTG rs143202281
NM_032682.5(FOXP1):c.*3413_*3414delTG rs143202281
NM_032682.5(FOXP1):c.*3413_*3414dupTG rs143202281
NM_032682.5(FOXP1):c.*3414_*3415insTGTGCG rs1553648184
NM_032682.5(FOXP1):c.*3415delCinsTGTGTGTGT rs886058827
NM_032682.5(FOXP1):c.*3415delCinsTGTGTGTGTGT rs886058827
NM_032682.5(FOXP1):c.*3416_*3417insTGTGTG rs886058826
NM_032682.5(FOXP1):c.*3417C>T rs201040980
NM_032682.5(FOXP1):c.*3419_*3420dupCG rs886058825
NM_032682.5(FOXP1):c.*3424G>A rs886058824
NM_032682.5(FOXP1):c.*3659T>A rs886058823
NM_032682.5(FOXP1):c.*3677_*3678insA rs886058822
NM_032682.5(FOXP1):c.*3722delT rs886058821
NM_032682.5(FOXP1):c.*4029delA rs753706183
NM_032682.5(FOXP1):c.*476delC rs886058861
NM_032682.5(FOXP1):c.*479_*480delCT rs886058859
NM_032682.5(FOXP1):c.*479delC rs886058860
NM_032682.5(FOXP1):c.*507_*509delTTT rs10633687
NM_032682.5(FOXP1):c.*509delT rs10633687
NM_032682.5(FOXP1):c.*510_*511delGC rs886058857
NM_032682.5(FOXP1):c.*510delG rs886058858
NM_032682.5(FOXP1):c.*511delC rs886058856
NM_032682.5(FOXP1):c.*567delA rs886058855
NM_032682.5(FOXP1):c.*58dupA rs886058863
NM_032682.5(FOXP1):c.*596delC rs886058854
NM_032682.5(FOXP1):c.*616C>T rs886058853
NM_032682.5(FOXP1):c.*740_*743dupAATG rs886058852
NM_032682.5(FOXP1):c.-249C>T rs886058866
NM_032682.5(FOXP1):c.-393G>A rs886058867
NM_032682.5(FOXP1):c.-441G>A rs886058868
NM_032682.5(FOXP1):c.-482G>C rs886058869
NM_032682.5(FOXP1):c.-494A>G rs886058870
NM_032682.5(FOXP1):c.-520T>A rs886058871
NM_032682.5(FOXP1):c.1129A>G (p.Lys377Glu) rs886058865
NM_032682.5(FOXP1):c.1147-9dupT rs774665288
NM_032682.5(FOXP1):c.1155G>A (p.Leu385=) rs368920983
NM_032682.5(FOXP1):c.1239C>T (p.Pro413=) rs761941921
NM_032682.5(FOXP1):c.1641A>G (p.Gln547=) rs886058864
NM_032682.5(FOXP1):c.216G>A (p.Gln72=) rs144347581
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866

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