ClinVar Miner

List of variants in gene FKTN reported as likely benign for Cardiovascular phenotype

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Total variants: 8
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HGVS dbSNP
NM_001079802.2(FKTN):c.1023G>A (p.Pro341=) rs146967918
NM_001079802.2(FKTN):c.102A>C (p.Thr34=) rs138740640
NM_001079802.2(FKTN):c.1297A>G (p.Thr433Ala) rs141918432
NM_001079802.2(FKTN):c.167G>A (p.Arg56His) rs146951171
NM_001079802.2(FKTN):c.444C>T (p.Asp148=) rs759808323
NM_001079802.2(FKTN):c.510G>A (p.Ala170=) rs187804924
NM_001079802.2(FKTN):c.668C>T (p.Thr223Ile) rs116105846
NM_001079802.2(FKTN):c.681G>A (p.Leu227=) rs142604625

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