ClinVar Miner

List of variants in gene HCN4 reported as likely benign for Brugada syndrome

Included ClinVar conditions (25):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 63
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HGVS dbSNP
NM_005477.3(HCN4):c.1014G>C (p.Leu338=) rs147771899
NM_005477.3(HCN4):c.102G>A (p.Glu34=) rs764116333
NM_005477.3(HCN4):c.1089C>T (p.Ile363=) rs140902511
NM_005477.3(HCN4):c.1090G>A (p.Asp364Asn) rs151004999
NM_005477.3(HCN4):c.1191T>C (p.Tyr397=) rs142643511
NM_005477.3(HCN4):c.1242C>T (p.Ala414=) rs376218786
NM_005477.3(HCN4):c.1254C>T (p.Ile418=) rs373794941
NM_005477.3(HCN4):c.1443C>T (p.Tyr481=) rs200337785
NM_005477.3(HCN4):c.1458C>T (p.Pro486=) rs760102595
NM_005477.3(HCN4):c.1509C>T (p.Ala503=) rs1060503837
NM_005477.3(HCN4):c.1548C>T (p.Leu516=) rs1060503838
NM_005477.3(HCN4):c.1557C>T (p.Ser519=) rs1555475972
NM_005477.3(HCN4):c.1560G>A (p.Leu520=) rs200033529
NM_005477.3(HCN4):c.1563C>T (p.Asp521=) rs201999732
NM_005477.3(HCN4):c.1656C>T (p.His552=) rs148142070
NM_005477.3(HCN4):c.1674C>A (p.Arg558=) rs201337528
NM_005477.3(HCN4):c.1703G>C (p.Ser568Thr) rs138714806
NM_005477.3(HCN4):c.1797G>A (p.Ala599=) rs371484779
NM_005477.3(HCN4):c.1815G>A (p.Thr605=) rs367753936
NM_005477.3(HCN4):c.1959C>T (p.Ala653=) rs371293769
NM_005477.3(HCN4):c.2016C>T (p.Ser672=) rs104894488
NM_005477.3(HCN4):c.2112G>A (p.Glu704=) rs746156652
NM_005477.3(HCN4):c.2115C>T (p.Thr705=) rs201652877
NM_005477.3(HCN4):c.2181C>T (p.His727=) rs140354126
NM_005477.3(HCN4):c.2210A>G (p.Gln737Arg) rs146732972
NM_005477.3(HCN4):c.2313C>T (p.Pro771=) rs142298104
NM_005477.3(HCN4):c.2349G>A (p.Gln783=) rs746658574
NM_005477.3(HCN4):c.2385C>T (p.Leu795=) rs878854773
NM_005477.3(HCN4):c.2465C>T (p.Thr822Met) rs201143364
NM_005477.3(HCN4):c.2523G>A (p.Ser841=) rs768157473
NM_005477.3(HCN4):c.2526C>T (p.Pro842=) rs201499694
NM_005477.3(HCN4):c.2604C>T (p.Pro868=) rs138773305
NM_005477.3(HCN4):c.2652C>T (p.Pro884=) rs373814254
NM_005477.3(HCN4):c.2694C>T (p.Gly898=) rs375169111
NM_005477.3(HCN4):c.2715C>T (p.Ala905=) rs745886315
NM_005477.3(HCN4):c.2733C>T (p.His911=) rs565795330
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465
NM_005477.3(HCN4):c.2830G>A (p.Ala944Thr) rs777648103
NM_005477.3(HCN4):c.2838C>T (p.Pro946=) rs552881314
NM_005477.3(HCN4):c.2901C>T (p.Ser967=) rs570068696
NM_005477.3(HCN4):c.2916C>T (p.Pro972=) rs559422705
NM_005477.3(HCN4):c.2997G>A (p.Arg999=) rs749040050
NM_005477.3(HCN4):c.3009G>A (p.Pro1003=) rs775401682
NM_005477.3(HCN4):c.3010C>T (p.Pro1004Ser) rs201418838
NM_005477.3(HCN4):c.3012G>A (p.Pro1004=) rs377602893
NM_005477.3(HCN4):c.3078C>T (p.Ser1026=) rs202188345
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=) rs749785521
NM_005477.3(HCN4):c.3126G>A (p.Pro1042=) rs1057521459
NM_005477.3(HCN4):c.3147C>T (p.His1049=) rs757396406
NM_005477.3(HCN4):c.3187C>A (p.Pro1063Thr) rs535227661
NM_005477.3(HCN4):c.3228C>T (p.Pro1076=) rs770161577
NM_005477.3(HCN4):c.3264G>A (p.Ala1088=) rs752705479
NM_005477.3(HCN4):c.3351G>A (p.Pro1117=) rs375138488
NM_005477.3(HCN4):c.3354C>T (p.Leu1118=) rs867816182
NM_005477.3(HCN4):c.3405C>T (p.Leu1135=) rs548860628
NM_005477.3(HCN4):c.3531G>T (p.Gly1177=) rs375911378
NM_005477.3(HCN4):c.453G>A (p.Glu151=) rs1162105115
NM_005477.3(HCN4):c.458A>G (p.Glu153Gly) rs560874115
NM_005477.3(HCN4):c.549G>T (p.Ser183=) rs767095274
NM_005477.3(HCN4):c.561T>C (p.Ala187=) rs375206856
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958
NM_005477.3(HCN4):c.954C>T (p.Ile318=) rs764050400
NM_005477.3(HCN4):c.972A>G (p.Thr324=) rs747884744

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