ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 79
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HGVS dbSNP gnomAD frequency
NM_001079802.2(FKTN):c.648-129T>A rs10978171 0.01897
NM_001079802.2(FKTN):c.*2298C>G rs116107812 0.01491
NM_001079802.2(FKTN):c.-88-247T>A rs145429432 0.01398
NM_001079802.2(FKTN):c.105+129del rs112124536 0.01337
NM_001079802.2(FKTN):c.648-1016C>G rs116042261 0.01301
NM_001079802.2(FKTN):c.*5517T>C rs114655654 0.01215
NM_001079802.2(FKTN):c.648-1146T>G rs116908450 0.01174
NM_001079802.2(FKTN):c.*818C>T rs79162268 0.01167
NM_001079802.2(FKTN):c.781-263C>T rs180878733 0.01016
NM_001079802.2(FKTN):c.106-40A>G rs79175958 0.01001
NM_001079802.2(FKTN):c.-88-344C>T rs74505742 0.00997
NM_001079802.2(FKTN):c.-180-228C>T rs116703997 0.00996
NM_001079802.2(FKTN):c.-180-242T>C rs115507264 0.00995
NM_001079802.2(FKTN):c.*1323C>T rs75764875 0.00992
NM_001079802.2(FKTN):c.*1638A>G rs78462952 0.00980
NM_001079802.2(FKTN):c.-89+243A>G rs78182480 0.00973
NM_001079802.2(FKTN):c.781-222dup rs368158605 0.00910
NM_001079802.2(FKTN):c.780+313C>T rs138420309 0.00844
NM_001079802.2(FKTN):c.*5578G>A rs41277801 0.00776
NM_001079802.2(FKTN):c.106-169A>G rs112290608 0.00739
NM_001079802.2(FKTN):c.648-1404C>T rs75075378 0.00715
NM_001079802.2(FKTN):c.-180-101G>C rs140838771 0.00622
NM_001079802.2(FKTN):c.-88-110T>A rs145125963 0.00605
NM_001079802.2(FKTN):c.105+40A>C rs181305205 0.00548
NM_001079802.2(FKTN):c.-89+120G>A rs74995479 0.00505
NM_001079802.2(FKTN):c.*2427G>T rs116364105 0.00472
NM_001079802.2(FKTN):c.648-950A>G rs188992967 0.00450
NM_001079802.2(FKTN):c.648-1278A>C rs181901044 0.00425
NM_001079802.2(FKTN):c.910+59A>G rs111443273 0.00399
NM_001079802.2(FKTN):c.370-252C>T rs372938103 0.00390
NM_001079802.2(FKTN):c.165+214T>A rs113105864 0.00372
NM_001079802.2(FKTN):c.106-245C>T rs111250428 0.00367
NM_001079802.2(FKTN):c.*3861T>C rs185745657 0.00292
NM_001079802.2(FKTN):c.647+36G>A rs115199403 0.00277
NM_001079802.2(FKTN):c.910+45C>T rs142323157 0.00270
NM_001079802.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432 0.00228
NM_001079802.2(FKTN):c.167G>A (p.Arg56His) rs146951171 0.00218
NM_001079802.2(FKTN):c.165+304A>G rs190815593 0.00170
NM_001079802.2(FKTN):c.166-4A>G rs193922689 0.00125
NM_001079802.2(FKTN):c.285T>C (p.His95=) rs148046151 0.00050
NM_001079802.2(FKTN):c.910+13C>T rs375259473 0.00026
NM_001079802.2(FKTN):c.102A>C (p.Thr34=) rs138740640 0.00025
NM_001079802.2(FKTN):c.-88-5C>T rs555754136 0.00011
NM_001079802.2(FKTN):c.647+12G>A rs372589966 0.00011
NM_001079802.2(FKTN):c.*4877T>C rs1390561303 0.00009
NM_001079802.2(FKTN):c.1172+13T>C rs768792475 0.00009
NM_001079802.2(FKTN):c.1248C>T (p.Leu416=) rs774804160 0.00004
NM_001079802.2(FKTN):c.1383T>C (p.Tyr461=) rs140899569 0.00004
NM_001079802.2(FKTN):c.207T>C (p.Asn69=) rs752921570 0.00004
NM_001079802.2(FKTN):c.911-8C>A rs749557617 0.00003
NM_001079802.2(FKTN):c.63G>C (p.Leu21=) rs766642997 0.00002
NM_001079802.2(FKTN):c.1195C>T (p.Leu399=) rs768867435 0.00001
NM_001079802.2(FKTN):c.1260A>G (p.Glu420=) rs1290782710 0.00001
NM_001079802.2(FKTN):c.198C>G (p.Ser66=) rs367868644 0.00001
NM_001079802.2(FKTN):c.21C>T (p.Asn7=) rs564632018 0.00001
NM_001079802.2(FKTN):c.357A>G (p.Leu119=) rs760933616 0.00001
NM_001079802.2(FKTN):c.855G>A (p.Ala285=) rs1057521448 0.00001
NM_001079802.2(FKTN):c.*1859G>C rs149725616
NM_001079802.2(FKTN):c.*2995T>G rs77017417
NM_001079802.2(FKTN):c.*5303dup rs879263714
NM_001079802.2(FKTN):c.*806G>C rs75971372
NM_001079802.2(FKTN):c.-180-102G>A rs116486520
NM_001079802.2(FKTN):c.-180-102G>T rs116486520
NM_001079802.2(FKTN):c.-180-15del rs796889209
NM_001079802.2(FKTN):c.-199C>T rs1589136419
NM_001079802.2(FKTN):c.-88-268_-88-266del rs143993607
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_001079802.2(FKTN):c.106-18C>T rs748663594
NM_001079802.2(FKTN):c.1172+86C>A rs142935024
NM_001079802.2(FKTN):c.1173A>G (p.Lys391=) rs2133450404
NM_001079802.2(FKTN):c.1185G>A (p.Pro395=) rs141886790
NM_001079802.2(FKTN):c.1269T>C (p.Tyr423=) rs1554766906
NM_001079802.2(FKTN):c.648-1102_648-1099dup rs386415742
NM_001079802.2(FKTN):c.766C>A (p.Arg256=) rs377417974
NM_001079802.2(FKTN):c.867C>T (p.Asn289=) rs1554757882
NM_001079802.2(FKTN):c.910+19T>G rs771773538
NM_001079802.2(FKTN):c.910+290T>G rs112299748
NM_001079802.2(FKTN):c.911-13A>G rs766103012
NM_001079802.2(FKTN):c.911-18dup rs757992747

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