ClinVar Miner

List of variants in gene FOXP1 reported as likely benign for History of neurodevelopmental disorder

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP
NM_032682.5(FOXP1):c.114C>T (p.Asn38=)
NM_032682.5(FOXP1):c.123G>A (p.Thr41=)
NM_032682.5(FOXP1):c.135C>T (p.Asp45=)
NM_032682.5(FOXP1):c.154G>A (p.Ala52Thr)
NM_032682.5(FOXP1):c.1652+4C>T
NM_032682.5(FOXP1):c.1702C>T (p.Pro568Ser) rs147674680
NM_032682.5(FOXP1):c.1709A>G (p.Asn570Ser) rs140161845
NM_032682.5(FOXP1):c.1825G>A (p.Ala609Thr)
NM_032682.5(FOXP1):c.1848C>T (p.Asn616=)
NM_032682.5(FOXP1):c.44C>T (p.Ala15Val) rs532329866
NM_032682.5(FOXP1):c.643C>G (p.Pro215Ala) rs146606219
NM_032682.5(FOXP1):c.676A>G (p.Thr226Ala)
NM_032682.5(FOXP1):c.738C>G (p.Gly246=)

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.