ClinVar Miner

List of variants in gene FKTN studied for Cardiovascular phenotype

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
NM_006731.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_006731.2(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_006731.2(FKTN):c.102A>C (p.Thr34=) rs138740640
NM_006731.2(FKTN):c.1159G>A (p.Gly387Arg) rs148975262
NM_006731.2(FKTN):c.1249G>A (p.Glu417Lys) rs765934383
NM_006731.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432
NM_006731.2(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_006731.2(FKTN):c.166C>T (p.Arg56Cys) rs41277797
NM_006731.2(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_006731.2(FKTN):c.22G>T (p.Val8Leu) rs368981218
NM_006731.2(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_006731.2(FKTN):c.374G>T (p.Gly125Val) rs142783718
NM_006731.2(FKTN):c.382C>T (p.Arg128Trp) rs767026996
NM_006731.2(FKTN):c.42G>A (p.Thr14=) rs78794935
NM_006731.2(FKTN):c.444C>T (p.Asp148=) rs759808323
NM_006731.2(FKTN):c.457C>G (p.Leu153Val) rs977350409
NM_006731.2(FKTN):c.510G>A (p.Ala170=) rs187804924
NM_006731.2(FKTN):c.608G>A (p.Arg203Gln) rs34787999
NM_006731.2(FKTN):c.625C>T (p.Arg209Cys) rs749576551
NM_006731.2(FKTN):c.668C>T (p.Thr223Ile) rs116105846
NM_006731.2(FKTN):c.681G>A (p.Leu227=) rs142604625
NM_006731.2(FKTN):c.895A>C (p.Ser299Arg) rs367662190

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.