ClinVar Miner

List of variants in gene FKTN reported as likely benign by GeneDx

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Gene type:
ClinVar version:
Total variants: 34
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HGVS dbSNP
NC_000009.12:g.105574673_105574675del
NM_006731.2(FKTN):c.-107C>T
NM_006731.2(FKTN):c.-88-247T>A
NM_006731.2(FKTN):c.102A>C (p.Thr34=) rs138740640
NM_006731.2(FKTN):c.105+129del
NM_006731.2(FKTN):c.106-169A>G
NM_006731.2(FKTN):c.106-18C>T rs748663594
NM_006731.2(FKTN):c.1172+13T>C rs768792475
NM_006731.2(FKTN):c.1185G>A (p.Pro395=) rs141886790
NM_006731.2(FKTN):c.1195C>T (p.Leu399=) rs768867435
NM_006731.2(FKTN):c.1248C>T (p.Leu416=) rs774804160
NM_006731.2(FKTN):c.1260A>G (p.Glu420=)
NM_006731.2(FKTN):c.1269T>C (p.Tyr423=) rs1554766906
NM_006731.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432
NM_006731.2(FKTN):c.1383T>C (p.Tyr461=)
NM_006731.2(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_006731.2(FKTN):c.198C>G (p.Ser66=) rs367868644
NM_006731.2(FKTN):c.21C>T (p.Asn7=) rs564632018
NM_006731.2(FKTN):c.285T>C (p.His95=) rs148046151
NM_006731.2(FKTN):c.357A>G (p.Leu119=) rs760933616
NM_006731.2(FKTN):c.647+12G>A rs372589966
NM_006731.2(FKTN):c.648-1016C>G
NM_006731.2(FKTN):c.648-1278A>C
NM_006731.2(FKTN):c.648-129T>A
NM_006731.2(FKTN):c.648-1404C>T
NM_006731.2(FKTN):c.766C>A (p.Arg256=) rs377417974
NM_006731.2(FKTN):c.781-263C>T
NM_006731.2(FKTN):c.855G>A (p.Ala285=) rs1057521448
NM_006731.2(FKTN):c.867C>T (p.Asn289=) rs1554757882
NM_006731.2(FKTN):c.910+13C>T rs375259473
NM_006731.2(FKTN):c.910+19T>G rs771773538
NM_006731.2(FKTN):c.911-13A>G rs766103012
NM_006731.2(FKTN):c.911-18dup rs757992747
NM_006731.2(FKTN):c.911-8C>A rs749557617

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