ClinVar Miner

List of variants reported as likely benign for Fukuyama congenital muscular dystrophy

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 16
Download table as spreadsheet
NM_001079802.2(FKTN):c.*1018T>A rs16924759
NM_001079802.2(FKTN):c.*1249C>T rs79589823
NM_001079802.2(FKTN):c.*2910C>A rs148937517
NM_001079802.2(FKTN):c.*4825T>C rs115155934
NM_001079802.2(FKTN):c.*818C>T rs79162268
NM_001079802.2(FKTN):c.-158G>C rs4742953
NM_001079802.2(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_001079802.2(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_001079802.2(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_001079802.2(FKTN):c.608G>A (p.Arg203Gln) rs34787999
NM_006731.2(FKTN):c.166-6A>G rs41277795
NM_006731.2(FKTN):c.910+14G>A rs76180538

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.