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:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
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HGVS dbSNP
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.1147-15dup rs774665288
NM_032682.6(FOXP1):c.*1027_*1030dup rs886058851
NM_032682.6(FOXP1):c.*1027_*1031CTTTT[2] rs549654259
NM_032682.6(FOXP1):c.*1037_*1040del rs886058850
NM_032682.6(FOXP1):c.*1049_*1050dup rs747818299
NM_032682.6(FOXP1):c.*1100T>C rs886058848
NM_032682.6(FOXP1):c.*1104C>A rs886058847
NM_032682.6(FOXP1):c.*1131T>G rs867338460
NM_032682.6(FOXP1):c.*119A>G rs886058862
NM_032682.6(FOXP1):c.*1208C>T rs771846939
NM_032682.6(FOXP1):c.*1209G>A rs886058846
NM_032682.6(FOXP1):c.*1231_*1235dup rs373349025
NM_032682.6(FOXP1):c.*1306G>A rs886058844
NM_032682.6(FOXP1):c.*1523G>T rs886058843
NM_032682.6(FOXP1):c.*1541dup rs570372825
NM_032682.6(FOXP1):c.*1669dup rs886058842
NM_032682.6(FOXP1):c.*1857A>G rs886058841
NM_032682.6(FOXP1):c.*2067A>G rs557236485
NM_032682.6(FOXP1):c.*2202_*2203GA[1] rs779139545
NM_032682.6(FOXP1):c.*2237G>A rs886058840
NM_032682.6(FOXP1):c.*2312T>C rs886058839
NM_032682.6(FOXP1):c.*2362A>G rs886058838
NM_032682.6(FOXP1):c.*2473T>A rs780171188
NM_032682.6(FOXP1):c.*2473_*2482del rs886058837
NM_032682.6(FOXP1):c.*2757dup rs886058836
NM_032682.6(FOXP1):c.*2831dup rs112098084
NM_032682.6(FOXP1):c.*2832del rs886058835
NM_032682.6(FOXP1):c.*2837dup rs886058834
NM_032682.6(FOXP1):c.*2979C>T rs886058833
NM_032682.6(FOXP1):c.*3192del rs535202716
NM_032682.6(FOXP1):c.*3303dup rs886058832
NM_032682.6(FOXP1):c.*3313T>C rs886058831
NM_032682.6(FOXP1):c.*3391_*3392TG[10] rs143202281
NM_032682.6(FOXP1):c.*3391_*3392TG[11] rs143202281
NM_032682.6(FOXP1):c.*3391_*3392TG[13] rs143202281
NM_032682.6(FOXP1):c.*3391_*3392TG[14] rs143202281
NM_032682.6(FOXP1):c.*3391_*3392TG[16] rs143202281
NM_032682.6(FOXP1):c.*3402G>A rs886058830
NM_032682.6(FOXP1):c.*3403del rs886058829
NM_032682.6(FOXP1):c.*3414_*3415insTGTGCG rs1553648184
NM_032682.6(FOXP1):c.*3415_*3416CG[4] rs886058825
NM_032682.6(FOXP1):c.*3415delinsTGTGTGTGT rs886058827
NM_032682.6(FOXP1):c.*3415delinsTGTGTGTGTGT rs886058827
NM_032682.6(FOXP1):c.*3417C>T rs201040980
NM_032682.6(FOXP1):c.*3417_*3418TG[3] rs886058826
NM_032682.6(FOXP1):c.*3424G>A rs886058824
NM_032682.6(FOXP1):c.*3659T>A rs886058823
NM_032682.6(FOXP1):c.*3677_*3678insA rs886058822
NM_032682.6(FOXP1):c.*3722del rs886058821
NM_032682.6(FOXP1):c.*4029del rs753706183
NM_032682.6(FOXP1):c.*476del rs886058861
NM_032682.6(FOXP1):c.*479_*480del rs886058859
NM_032682.6(FOXP1):c.*479del rs886058860
NM_032682.6(FOXP1):c.*507_*509del rs10633687
NM_032682.6(FOXP1):c.*509del rs10633687
NM_032682.6(FOXP1):c.*510_*511del rs886058857
NM_032682.6(FOXP1):c.*510del rs886058858
NM_032682.6(FOXP1):c.*511del rs886058856
NM_032682.6(FOXP1):c.*567del rs886058855
NM_032682.6(FOXP1):c.*58dup rs886058863
NM_032682.6(FOXP1):c.*596del rs886058854
NM_032682.6(FOXP1):c.*616C>T rs886058853
NM_032682.6(FOXP1):c.*740_*743dup rs886058852
NM_032682.6(FOXP1):c.-249C>T rs886058866
NM_032682.6(FOXP1):c.-393G>A rs886058867
NM_032682.6(FOXP1):c.-441G>A rs886058868
NM_032682.6(FOXP1):c.1129A>G (p.Lys377Glu) rs886058865
NM_032682.6(FOXP1):c.1155G>A (p.Leu385=) rs368920983
NM_032682.6(FOXP1):c.1239C>T (p.Pro413=) rs761941921
NM_032682.6(FOXP1):c.1641A>G (p.Gln547=) rs886058864
NM_032682.6(FOXP1):c.216G>A (p.Gln72=) rs144347581
NM_032682.6(FOXP1):c.44C>T (p.Ala15Val) rs532329866

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