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

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 36

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HGVS	dbSNP	gnomAD frequency
NM_001079802.2(FKTN):c.1026C>A (p.Leu342=)	rs17309806	0.27837
NM_001079802.2(FKTN):c.608G>A (p.Arg203Gln)	rs34787999	0.25357
NM_001079802.2(FKTN):c.166C>T (p.Arg56Cys)	rs41277797	0.02093
NM_001079802.2(FKTN):c.106-10G>A	rs148384394	0.01000
NM_001079802.2(FKTN):c.1336A>G (p.Asn446Asp)	rs41313301	0.00809
NM_001079802.2(FKTN):c.166-6A>G	rs41277795	0.00808
NM_001079802.2(FKTN):c.910+14G>A	rs76180538	0.00806
NM_001079802.2(FKTN):c.1045-40C>A	rs145883833	0.00284
NM_001079802.2(FKTN):c.1297A>G (p.Thr433Ala)	rs141918432	0.00228
NM_001079802.2(FKTN):c.668C>T (p.Thr223Ile)	rs116105846	0.00224
NM_001079802.2(FKTN):c.167G>A (p.Arg56His)	rs146951171	0.00218
NM_001079802.2(FKTN):c.681G>A (p.Leu227=)	rs142604625	0.00084
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.333T>C (p.Thr111=)	rs141729611	0.00015
NM_001079802.2(FKTN):c.647+12G>A	rs372589966	0.00011
NM_001079802.2(FKTN):c.1172+13T>C	rs768792475	0.00009
NM_001079802.2(FKTN):c.370-50T>C	rs139910824	0.00005
NM_001079802.2(FKTN):c.1248C>T (p.Leu416=)	rs774804160	0.00004
NM_001079802.2(FKTN):c.207T>C (p.Asn69=)	rs752921570	0.00004
NM_001079802.2(FKTN):c.444C>T (p.Asp148=)	rs759808323	0.00004
NM_001079802.2(FKTN):c.342A>G (p.Ala114=)	rs368598407	0.00002
NM_001079802.2(FKTN):c.1195C>T (p.Leu399=)	rs768867435	0.00001
NM_001079802.2(FKTN):c.198C>G (p.Ser66=)	rs367868644	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.*4388del	rs148253503
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=)	rs146967918
NM_001079802.2(FKTN):c.106-18C>T	rs748663594
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.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.911-18dup	rs757992747

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