ClinVar Miner

List of variants in gene FOXP1 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
Download table as spreadsheet
HGVS dbSNP
NM_032682.5(FOXP1):c.1064T>C (p.Leu355Pro) rs1064795306
NM_032682.5(FOXP1):c.1146+1G>T
NM_032682.5(FOXP1):c.1177A>T (p.Lys393Ter) rs1553668839
NM_032682.5(FOXP1):c.1348G>A (p.Ala450Thr) rs1553668386
NM_032682.5(FOXP1):c.1506C>G (p.Phe502Leu) rs1057524152
NM_032682.5(FOXP1):c.1653_1672dup (p.Asn558fs) rs1559596699
NM_032682.5(FOXP1):c.1710_1722+2del rs1559596230
NM_032682.5(FOXP1):c.1722+1G>A rs1553660900
NM_032682.5(FOXP1):c.1889+5G>T rs1553656383

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.