ClinVar Miner

List of variants in gene FKTN studied for Cardiovascular phenotype

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Total variants: 22
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HGVS dbSNP
NM_006731.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_006731.2(FKTN):c.1026C>A (p.Leu342=) rs17309806
NM_006731.2(FKTN):c.102A>C (p.Thr34=) rs138740640
NM_006731.2(FKTN):c.1159G>A (p.Gly387Arg) rs148975262
NM_006731.2(FKTN):c.1249G>A (p.Glu417Lys) rs765934383
NM_006731.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432
NM_006731.2(FKTN):c.1336A>G (p.Asn446Asp) rs41313301
NM_006731.2(FKTN):c.166C>T (p.Arg56Cys) rs41277797
NM_006731.2(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_006731.2(FKTN):c.22G>T (p.Val8Leu) rs368981218
NM_006731.2(FKTN):c.373G>A (p.Gly125Ser) rs34006675
NM_006731.2(FKTN):c.374G>T (p.Gly125Val) rs142783718
NM_006731.2(FKTN):c.382C>T (p.Arg128Trp) rs767026996
NM_006731.2(FKTN):c.42G>A (p.Thr14=) rs78794935
NM_006731.2(FKTN):c.444C>T (p.Asp148=) rs759808323
NM_006731.2(FKTN):c.457C>G (p.Leu153Val) rs977350409
NM_006731.2(FKTN):c.510G>A (p.Ala170=) rs187804924
NM_006731.2(FKTN):c.608G>A (p.Arg203Gln) rs34787999
NM_006731.2(FKTN):c.625C>T (p.Arg209Cys) rs749576551
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.895A>C (p.Ser299Arg) rs367662190

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