ClinVar Miner

List of variants in gene FKTN studied for not specified

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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_001079802.1(FKTN):c.*2280T>C rs1024366
NM_001079802.1(FKTN):c.*4388delA rs148253503
NM_001079802.1(FKTN):c.*4825T>C rs115155934
NM_001079802.1(FKTN):c.-108A>T rs191502146
NM_001079802.1(FKTN):c.-191_-191delT rs138776494
NM_001079802.1(FKTN):c.-45G>T rs77013649
NM_001079802.1(FKTN):c.-77A>G rs188804693
NM_001079802.1(FKTN):c.-88-6T>C rs115730708
NM_001079802.1(FKTN):c.-90delA rs727502845
NM_001079802.1(FKTN):c.-96T>C rs151250905
NM_001079802.1(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_001079802.1(FKTN):c.102A>C (p.Thr34=) rs138740640
NM_001079802.1(FKTN):c.106-10G>A rs148384394
NM_001079802.1(FKTN):c.106-18C>T rs748663594
NM_001079802.1(FKTN):c.106-40A>G rs79175958
NM_001079802.1(FKTN):c.1172+13T>C rs768792475
NM_001079802.1(FKTN):c.1185G>A (p.Pro395=) rs141886790
NM_001079802.1(FKTN):c.1195C>T (p.Leu399=) rs768867435
NM_001079802.1(FKTN):c.1248C>T (p.Leu416=) rs774804160
NM_001079802.1(FKTN):c.1269T>C (p.Tyr423=) rs1554766906
NM_001079802.1(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_001079802.1(FKTN):c.166-6A>G rs41277795
NM_001079802.1(FKTN):c.166C>T (p.Arg56Cys) rs41277797
NM_001079802.1(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_001079802.1(FKTN):c.198C>G (p.Ser66=) rs367868644
NM_001079802.1(FKTN):c.21C>T (p.Asn7=) rs564632018
NM_001079802.1(FKTN):c.285T>C (p.His95=) rs148046151
NM_001079802.1(FKTN):c.333T>C (p.Thr111=) rs141729611
NM_001079802.1(FKTN):c.357A>G (p.Leu119=) rs760933616
NM_001079802.1(FKTN):c.370-7G>A rs797045577
NM_001079802.1(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_001079802.1(FKTN):c.42G>A (p.Thr14=) rs78794935
NM_001079802.1(FKTN):c.508G>A (p.Ala170Thr) rs778818366
NM_001079802.1(FKTN):c.608G>A (p.Arg203Gln) rs34787999
NM_001079802.1(FKTN):c.647+12G>A rs372589966
NM_001079802.1(FKTN):c.668C>T (p.Thr223Ile) rs116105846
NM_001079802.1(FKTN):c.681G>A (p.Leu227=) rs142604625
NM_001079802.1(FKTN):c.766C>A (p.Arg256=) rs377417974
NM_001079802.1(FKTN):c.855G>A (p.Ala285=) rs1057521448
NM_001079802.1(FKTN):c.867C>T (p.Asn289=) rs1554757882
NM_001079802.1(FKTN):c.910+13C>T rs375259473
NM_001079802.1(FKTN):c.910+14G>A rs76180538
NM_001079802.1(FKTN):c.910+19T>G rs771773538
NM_001079802.1(FKTN):c.911-13A>G rs766103012
NM_001079802.1(FKTN):c.911-8C>A rs749557617
NM_006731.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_006731.2(FKTN):c.1044+44A>G rs118064041
NM_006731.2(FKTN):c.1045-40C>A rs145883833
NM_006731.2(FKTN):c.1186A>C (p.Lys396Gln) rs1477740717
NM_006731.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432
NM_006731.2(FKTN):c.166-4A>G rs193922689
NM_006731.2(FKTN):c.370-50T>C rs139910824
NM_006731.2(FKTN):c.588C>T (p.Asp196=) rs1222153269
NM_006731.2(FKTN):c.911-18dup rs757992747

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