ClinVar Miner

List of variants in gene HCN1 reported as likely benign for not provided

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Gene type:
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Total variants: 40
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HGVS dbSNP gnomAD frequency
NM_021072.4(HCN1):c.1619-210A>T rs774992569 0.02905
NM_021072.4(HCN1):c.1619-211T>A rs866912042 0.02308
NM_021072.4(HCN1):c.1783+88A>C rs112886466 0.01072
NM_021072.4(HCN1):c.1377+33A>G rs115647789 0.00746
NM_021072.4(HCN1):c.425+158C>T rs113860027 0.00709
NM_021072.4(HCN1):c.850-286_850-285insTATA rs374836434 0.00588
NM_021072.4(HCN1):c.1012-14A>G rs112775315 0.00521
NM_021072.4(HCN1):c.1784-115T>G rs188999686 0.00468
NM_021072.4(HCN1):c.140G>T (p.Gly47Val) rs544994462 0.00362
NM_021072.4(HCN1):c.1012-37A>T rs113964925 0.00359
NM_021072.4(HCN1):c.1783+4C>T rs188586020 0.00196
NM_021072.4(HCN1):c.2172C>T (p.Ala724=) rs56217199 0.00191
NM_021072.4(HCN1):c.124C>T (p.Pro42Ser) rs56164833 0.00035
NM_021072.4(HCN1):c.240C>A (p.Gly80=) rs373664268 0.00032
NM_021072.4(HCN1):c.1626C>T (p.Cys542=) rs150863293 0.00023
NM_021072.4(HCN1):c.24C>T (p.Asn8=) rs753690439 0.00015
NM_021072.4(HCN1):c.1521C>T (p.Ala507=) rs55642950 0.00013
NM_021072.4(HCN1):c.726A>C (p.Gly242=) rs199622227 0.00003
NM_021072.4(HCN1):c.1065C>T (p.His355=) rs200829129 0.00001
NM_021072.4(HCN1):c.1578C>A (p.Ser526=) rs1478297290 0.00001
NM_021072.4(HCN1):c.1980G>A (p.Met660Ile) rs1335934380 0.00001
NM_021072.3:c.850-?_1377+?del
NM_021072.4(HCN1):c.-279C>T rs78789554
NM_021072.4(HCN1):c.1545T>C (p.Ile515=)
NM_021072.4(HCN1):c.159C>T (p.His53=) rs10066808
NM_021072.4(HCN1):c.1619-211del rs375114789
NM_021072.4(HCN1):c.1638A>G (p.Lys546=) rs1744876391
NM_021072.4(HCN1):c.1783+545G>A
NM_021072.4(HCN1):c.189C>T (p.Gly63=) rs1580055249
NM_021072.4(HCN1):c.192TGGCGGCGG[3] (p.Gly72_Gly74dup) rs56064803
NM_021072.4(HCN1):c.1977C>A (p.Arg659=)
NM_021072.4(HCN1):c.203GCG[10] (p.Gly72_Gly74dup) rs747975797
NM_021072.4(HCN1):c.203GCG[4] (p.Gly72_Gly74del) rs747975797
NM_021072.4(HCN1):c.203GCG[5] (p.Gly73_Gly74del) rs747975797
NM_021072.4(HCN1):c.2163C>T (p.Ser721=)
NM_021072.4(HCN1):c.2427C>A (p.Gly809=)
NM_021072.4(HCN1):c.2556G>T (p.Pro852=) rs1341530184
NM_021072.4(HCN1):c.336C>A (p.Arg112=) rs794726951
NM_021072.4(HCN1):c.425+245G>C rs561646796
NM_021072.4(HCN1):c.687C>A (p.Ser229=) rs1442056712

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