ClinVar Miner

List of variants in gene FKTN reported as benign for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 23
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HGVS dbSNP
NM_006731.2(FKTN):c.*2280T>C rs1024366
NM_006731.2(FKTN):c.*4825T>C rs115155934
NM_006731.2(FKTN):c.-45G>T rs77013649
NM_006731.2(FKTN):c.-77A>G rs188804693
NM_006731.2(FKTN):c.-88-1200del rs727502845
NM_006731.2(FKTN):c.-88-1206T>C rs151250905
NM_006731.2(FKTN):c.-88-1218A>T rs191502146
NM_006731.2(FKTN):c.-88-6T>C rs115730708
NM_006731.2(FKTN):c.-99del rs138776494
NM_006731.2(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_006731.2(FKTN):c.1044+44A>G rs118064041
NM_006731.2(FKTN):c.1045-40C>A rs145883833
NM_006731.2(FKTN):c.106-10G>A rs148384394
NM_006731.2(FKTN):c.106-40A>G rs79175958
NM_006731.2(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_006731.2(FKTN):c.166-6A>G rs41277795
NM_006731.2(FKTN):c.166C>T (p.Arg56Cys) rs41277797
NM_006731.2(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_006731.2(FKTN):c.42G>A (p.Thr14=) rs78794935
NM_006731.2(FKTN):c.608G>A (p.Arg203Gln) rs34787999
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.910+14G>A rs76180538

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