ClinVar Miner

List of variants in gene HCN4 reported by PreventionGenetics, part of Exact Sciences

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Gene type:
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Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.3600A>G (p.Pro1200=) rs529004 0.88237
NM_005477.3(HCN4):c.1979-41A>G rs481579 0.80894
NM_005477.3(HCN4):c.1558C>T (p.Leu520=) rs12909882 0.07848
NM_005477.3(HCN4):c.2556G>A (p.Pro852=) rs117819825 0.04888
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu) rs143090627 0.04452
NM_005477.3(HCN4):c.3337A>G (p.Met1113Val) rs142735148 0.00983
NM_005477.3(HCN4):c.36C>G (p.Leu12=) rs201193660 0.00635
NM_005477.3(HCN4):c.2601C>A (p.Ala867=) rs143188160 0.00352
NM_005477.3(HCN4):c.2657C>T (p.Ala886Val) rs200575377 0.00352
NM_005477.3(HCN4):c.1518C>T (p.Tyr506=) rs139590882 0.00163
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115 0.00149
NM_005477.3(HCN4):c.3010C>T (p.Pro1004Ser) rs201418838 0.00084
NM_005477.3(HCN4):c.3577G>C (p.Glu1193Gln) rs200507617 0.00068
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465 0.00045
NM_005477.3(HCN4):c.1635C>T (p.Pro545=) rs140015730 0.00024
NM_005477.3(HCN4):c.2109C>T (p.Phe703=) rs150378994 0.00021
NM_005477.3(HCN4):c.302C>T (p.Ala101Val) rs781730381 0.00018
NM_005477.3(HCN4):c.2730C>A (p.Phe910Leu) rs200814534 0.00014
NM_005477.3(HCN4):c.2838C>T (p.Pro946=) rs552881314 0.00011
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=) rs749785521 0.00011
NM_005477.3(HCN4):c.2669C>T (p.Pro890Leu) rs758929649 0.00008
NM_005477.3(HCN4):c.1243G>A (p.Val415Met) rs201978086 0.00007
NM_005477.3(HCN4):c.1303C>T (p.Leu435=) rs746461789 0.00006
NM_005477.3(HCN4):c.1512C>T (p.Thr504=) rs754956009 0.00006
NM_005477.3(HCN4):c.2652C>T (p.Pro884=) rs373814254 0.00006
NM_005477.3(HCN4):c.2917G>A (p.Gly973Arg) rs200495478 0.00006
NM_005477.3(HCN4):c.537C>T (p.Cys179=) rs753829397 0.00006
NM_005477.3(HCN4):c.1254C>T (p.Ile418=) rs373794941 0.00005
NM_005477.3(HCN4):c.394A>C (p.Ile132Leu) rs772764704 0.00004
NM_005477.3(HCN4):c.1401C>T (p.Tyr467=) rs753580737 0.00002
NM_005477.3(HCN4):c.1871G>A (p.Arg624Gln) rs763842368 0.00002
NM_005477.3(HCN4):c.2916C>T (p.Pro972=) rs559422705 0.00002
NM_005477.3(HCN4):c.375C>T (p.Ser125=) rs1310424203 0.00002
NM_005477.3(HCN4):c.1459G>A (p.Val487Met) rs202037304 0.00001
NM_005477.3(HCN4):c.2523G>A (p.Ser841=) rs768157473 0.00001
NM_005477.3(HCN4):c.3064C>T (p.Arg1022Ter) rs762950777 0.00001
NM_005477.3(HCN4):c.3294G>A (p.Ala1098=) rs766077921 0.00001
NM_005477.3(HCN4):c.1433G>A (p.Cys478Tyr)
NM_005477.3(HCN4):c.1471G>A (p.Asp491Asn) rs1060500107
NM_005477.3(HCN4):c.2143+10A>T
NM_005477.3(HCN4):c.252G>A (p.Ala84=) rs2043137516
NM_005477.3(HCN4):c.2700C>A (p.Ala900=) rs377656260
NM_005477.3(HCN4):c.3214C>T (p.Pro1072Ser)
NM_005477.3(HCN4):c.3532C>T (p.Pro1178Ser) rs1354805701
NM_005477.3(HCN4):c.82G>A (p.Glu28Lys) rs867068803

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