List of variants in gene FOXP1 reported as uncertain significance by Illumina Laboratory Services, Illumina

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 43

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HGVS	dbSNP	gnomAD frequency
NM_001349338.3(FOXP1):c.2473_2482del	rs886058837	0.00251
NM_001349338.3(FOXP1):c.*3403del	rs886058829	0.00001
NM_001349338.3(FOXP1):c.*1027CTTTT[2]	rs549654259
NM_001349338.3(FOXP1):c.1027_1030dup	rs886058851
NM_001349338.3(FOXP1):c.1037_1040del	rs886058850
NM_001349338.3(FOXP1):c.1049_1050dup	rs747818299
NM_001349338.3(FOXP1):c.1231_1235dup	rs373349025
NM_001349338.3(FOXP1):c.*1541dup	rs570372825
NM_001349338.3(FOXP1):c.*1669dup	rs886058842
NM_001349338.3(FOXP1):c.*2202GA[1]	rs779139545
NM_001349338.3(FOXP1):c.*2757dup	rs886058836
NM_001349338.3(FOXP1):c.*2831dup	rs112098084
NM_001349338.3(FOXP1):c.*2832del	rs886058835
NM_001349338.3(FOXP1):c.*2837dup	rs886058834
NM_001349338.3(FOXP1):c.*3192del	rs535202716
NM_001349338.3(FOXP1):c.*3303dup	rs886058832
NM_001349338.3(FOXP1):c.*3391TG[10]	rs143202281
NM_001349338.3(FOXP1):c.*3391TG[11]	rs143202281
NM_001349338.3(FOXP1):c.*3391TG[13]	rs143202281
NM_001349338.3(FOXP1):c.*3391TG[14]	rs143202281
NM_001349338.3(FOXP1):c.*3391TG[16]	rs143202281
NM_001349338.3(FOXP1):c.*3414GT[2]GCG[1]	rs1553648184
NM_001349338.3(FOXP1):c.*3415CG[4]	rs886058825
NM_001349338.3(FOXP1):c.*3415delinsTGTGTGTGT	rs886058827
NM_001349338.3(FOXP1):c.*3415delinsTGTGTGTGTGT	rs886058827
NM_001349338.3(FOXP1):c.*3417TG[3]	rs886058826
NM_001349338.3(FOXP1):c.3677_3678insA	rs886058822
NM_001349338.3(FOXP1):c.*3722del	rs886058821
NM_001349338.3(FOXP1):c.*4029del	rs753706183
NM_001349338.3(FOXP1):c.*476del	rs886058861
NM_001349338.3(FOXP1):c.479_480del	rs886058859
NM_001349338.3(FOXP1):c.*479del	rs886058860
NM_001349338.3(FOXP1):c.507_509del	rs10633687
NM_001349338.3(FOXP1):c.*509del	rs10633687
NM_001349338.3(FOXP1):c.510_511del	rs886058857
NM_001349338.3(FOXP1):c.*510del	rs886058858
NM_001349338.3(FOXP1):c.*511del	rs886058856
NM_001349338.3(FOXP1):c.*567del	rs886058855
NM_001349338.3(FOXP1):c.*58dup	rs886058863
NM_001349338.3(FOXP1):c.*596del	rs886058854
NM_001349338.3(FOXP1):c.740_743dup	rs886058852
NM_001349338.3(FOXP1):c.1147-9dup	rs774665288
NM_001349338.3(FOXP1):c.1538T>C (p.Val513Ala)	rs1553663140

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