ClinVar Miner

List of variants in gene KCNE5 reported as likely benign for Brugada syndrome

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Total variants: 22
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HGVS dbSNP gnomAD frequency
NM_012282.4(KCNE5):c.346G>A (p.Ala116Thr) rs764993726 0.00047
NM_012282.4(KCNE5):c.325C>T (p.Leu109=) rs767463268 0.00010
NM_012282.4(KCNE5):c.334G>A (p.Asp112Asn) rs764564753 0.00008
NM_012282.4(KCNE5):c.42C>T (p.Ser14=) rs763118222 0.00006
NM_012282.4(KCNE5):c.123C>T (p.Val41=) rs919650074 0.00004
NM_012282.4(KCNE5):c.387C>G (p.Ser129=) rs982739595 0.00002
NM_012282.4(KCNE5):c.49T>C (p.Leu17=) rs759549899 0.00002
NM_012282.4(KCNE5):c.168C>T (p.Gly56=) rs1934266907 0.00001
NM_012282.4(KCNE5):c.285C>T (p.Ser95=) rs750371428 0.00001
NM_012282.4(KCNE5):c.135T>C (p.Pro45=)
NM_012282.4(KCNE5):c.147C>T (p.Arg49=) rs2147333975
NM_012282.4(KCNE5):c.186C>T (p.Tyr62=)
NM_012282.4(KCNE5):c.24G>T (p.Arg8=) rs2147334108
NM_012282.4(KCNE5):c.264C>T (p.Val88=)
NM_012282.4(KCNE5):c.315G>A (p.Pro105=) rs2147333826
NM_012282.4(KCNE5):c.327G>C (p.Leu109=)
NM_012282.4(KCNE5):c.339C>T (p.Ala113=)
NM_012282.4(KCNE5):c.33C>T (p.Thr11=) rs1603395902
NM_012282.4(KCNE5):c.351G>A (p.Ala117=)
NM_012282.4(KCNE5):c.396G>C (p.Leu132=) rs1196378792
NM_012282.4(KCNE5):c.54C>T (p.Leu18=)
NM_012282.4(KCNE5):c.81C>T (p.Ser27=)

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