ClinVar Miner

List of variants in gene FOXP1 reported as uncertain significance for Inborn genetic diseases

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 21
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001349338.3(FOXP1):c.1135G>A (p.Ala379Thr) rs149759021 0.00008
NM_001349338.3(FOXP1):c.1239_1265dup (p.Leu414_Ser422dup) rs2107316260
NM_001349338.3(FOXP1):c.1256A>G (p.Gln419Arg)
NM_001349338.3(FOXP1):c.135C>A (p.Asp45Glu)
NM_001349338.3(FOXP1):c.1538T>C (p.Val513Ala) rs1553663140
NM_001349338.3(FOXP1):c.153CGCCCA[3] (p.His53_Ala54dup) rs1560101657
NM_001349338.3(FOXP1):c.1549C>T (p.Leu517Phe)
NM_001349338.3(FOXP1):c.1631G>A (p.Arg544Gln) rs2036497448
NM_001349338.3(FOXP1):c.1732G>A (p.Ala578Thr) rs2034696345
NM_001349338.3(FOXP1):c.1739A>G (p.Asn580Ser)
NM_001349338.3(FOXP1):c.1783C>G (p.Leu595Val)
NM_001349338.3(FOXP1):c.180+4C>T
NM_001349338.3(FOXP1):c.1872A>T (p.Arg624Ser)
NM_001349338.3(FOXP1):c.1903G>A (p.Val635Ile)
NM_001349338.3(FOXP1):c.1936G>A (p.Glu646Lys) rs756987886
NM_001349338.3(FOXP1):c.299C>T (p.Ala100Val)
NM_001349338.3(FOXP1):c.319A>G (p.Ile107Val) rs1440752852
NM_001349338.3(FOXP1):c.574C>A (p.Gln192Lys)
NM_001349338.3(FOXP1):c.602G>A (p.Arg201His) rs1450448594
NM_001349338.3(FOXP1):c.840G>C (p.Gln280His)
NM_001349338.3(FOXP1):c.983A>G (p.Asn328Ser)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.