ClinVar Miner

List of variants studied for Combined immunodeficiency due to moesin deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 7
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_002444.3(MSN):c.1056del (p.Lys352fs) rs2147518591
NM_002444.3(MSN):c.1099G>A (p.Glu367Lys)
NM_002444.3(MSN):c.1601A>C (p.Asp534Ala) rs1602878106
NM_002444.3(MSN):c.1657C>T (p.Arg553Ter) rs1057519075
NM_002444.3(MSN):c.511C>T (p.Arg171Trp) rs1057519074
NM_002444.3(MSN):c.817C>T (p.Arg273Trp) rs1441590143
NM_002444.3(MSN):c.877C>T (p.Arg293Cys)

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.