ClinVar Miner

List of variants reported as likely benign for Brugada syndrome 8

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 224
Download table as spreadsheet
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.1095G>A (p.Ser365=)
NM_005477.3(HCN4):c.1120C>T (p.Leu374=)
NM_005477.3(HCN4):c.1191T>C (p.Tyr397=) rs142643511
NM_005477.3(HCN4):c.1227C>T (p.Tyr409=) rs562792789
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.1278C>G (p.Leu426=)
NM_005477.3(HCN4):c.1303C>T (p.Leu435=) rs746461789
NM_005477.3(HCN4):c.1308G>A (p.Gln436=)
NM_005477.3(HCN4):c.1338T>G (p.Pro446=) rs780604251
NM_005477.3(HCN4):c.1341C>T (p.Asp447=)
NM_005477.3(HCN4):c.1404G>A (p.Ala468=)
NM_005477.3(HCN4):c.1407C>G (p.Leu469=)
NM_005477.3(HCN4):c.1437C>T (p.Ile479=) rs202001597
NM_005477.3(HCN4):c.1443C>T (p.Tyr481=) rs200337785
NM_005477.3(HCN4):c.144C>T (p.Ile48=)
NM_005477.3(HCN4):c.1455G>A (p.Ala485=) rs148875639
NM_005477.3(HCN4):c.1458C>T (p.Pro486=) rs760102595
NM_005477.3(HCN4):c.1482C>T (p.Leu494=) rs1041707015
NM_005477.3(HCN4):c.1485C>A (p.Thr495=)
NM_005477.3(HCN4):c.1491C>T (p.Leu497=) rs1260804406
NM_005477.3(HCN4):c.1509C>T (p.Ala503=) rs1060503837
NM_005477.3(HCN4):c.1512C>T (p.Thr504=)
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.1572G>T (p.Arg524=)
NM_005477.3(HCN4):c.157C>T (p.Leu53=) rs1595837657
NM_005477.3(HCN4):c.1590+10C>T
NM_005477.3(HCN4):c.1590+7C>G rs1595822862
NM_005477.3(HCN4):c.1591-7G>A
NM_005477.3(HCN4):c.1591-9C>T
NM_005477.3(HCN4):c.1593C>T (p.Tyr531=) rs958995249
NM_005477.3(HCN4):c.159G>A (p.Leu53=)
NM_005477.3(HCN4):c.1632G>A (p.Pro544=) rs544585089
NM_005477.3(HCN4):c.1635C>T (p.Pro545=) rs140015730
NM_005477.3(HCN4):c.1656C>T (p.His552=) rs148142070
NM_005477.3(HCN4):c.1665C>T (p.Tyr555=)
NM_005477.3(HCN4):c.1668G>A (p.Glu556=)
NM_005477.3(HCN4):c.1674C>A (p.Arg558=) rs201337528
NM_005477.3(HCN4):c.1695C>T (p.Asp565=)
NM_005477.3(HCN4):c.1703G>C (p.Ser568Thr) rs138714806
NM_005477.3(HCN4):c.1704C>T (p.Ser568=)
NM_005477.3(HCN4):c.171C>A (p.Ser57=)
NM_005477.3(HCN4):c.1728C>T (p.Pro576=)
NM_005477.3(HCN4):c.1729C>T (p.Leu577=) rs1057523463
NM_005477.3(HCN4):c.1738-5G>T
NM_005477.3(HCN4):c.1738-6C>T rs760763085
NM_005477.3(HCN4):c.1738-8T>C
NM_005477.3(HCN4):c.174C>A (p.Pro58=) rs920292438
NM_005477.3(HCN4):c.174C>T (p.Pro58=)
NM_005477.3(HCN4):c.1794T>C (p.Asn598=)
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.1854T>C (p.Pro618=)
NM_005477.3(HCN4):c.18G>T (p.Pro6=) rs771607645
NM_005477.3(HCN4):c.1924G>A (p.Val642Met) rs779402752
NM_005477.3(HCN4):c.1953G>A (p.Lys651=)
NM_005477.3(HCN4):c.1959C>T (p.Ala653=) rs371293769
NM_005477.3(HCN4):c.1962C>T (p.Asp654=)
NM_005477.3(HCN4):c.1971C>T (p.Tyr657=)
NM_005477.3(HCN4):c.1978+10C>G rs1595820799
NM_005477.3(HCN4):c.198G>A (p.Glu66=) rs772890780
NM_005477.3(HCN4):c.2016C>T (p.Ser672=) rs104894488
NM_005477.3(HCN4):c.2025C>T (p.Ala675=) rs149033101
NM_005477.3(HCN4):c.2028C>T (p.Asp676=) rs1060500102
NM_005477.3(HCN4):c.2049G>A (p.Ser683=) rs1407849744
NM_005477.3(HCN4):c.2052G>A (p.Leu684=)
NM_005477.3(HCN4):c.2055C>T (p.Ser685=) rs886042819
NM_005477.3(HCN4):c.2063A>G (p.Asn688Ser)
NM_005477.3(HCN4):c.2109C>T (p.Phe703=) rs150378994
NM_005477.3(HCN4):c.2112G>A (p.Glu704=) rs746156652
NM_005477.3(HCN4):c.2115C>G (p.Thr705=)
NM_005477.3(HCN4):c.2115C>T (p.Thr705=) rs201652877
NM_005477.3(HCN4):c.2121G>A (p.Ala707=) rs1354885005
NM_005477.3(HCN4):c.2139C>A (p.Arg713=)
NM_005477.3(HCN4):c.2143+5G>T rs547362030
NM_005477.3(HCN4):c.216C>G (p.Leu72=)
NM_005477.3(HCN4):c.2181C>T (p.His727=) rs140354126
NM_005477.3(HCN4):c.2193C>T (p.Ser731=) rs373015590
NM_005477.3(HCN4):c.2196C>T (p.Gly732=) rs780923169
NM_005477.3(HCN4):c.2210A>G (p.Gln737Arg) rs146732972
NM_005477.3(HCN4):c.2266G>A (p.Ala756Thr) rs143339036
NM_005477.3(HCN4):c.2274C>T (p.Arg758=) rs749766433
NM_005477.3(HCN4):c.2283T>G (p.Ala761=)
NM_005477.3(HCN4):c.228C>T (p.Asp76=)
NM_005477.3(HCN4):c.2310G>A (p.Thr770=)
NM_005477.3(HCN4):c.2313C>T (p.Pro771=) rs142298104
NM_005477.3(HCN4):c.231C>T (p.Ser77=)
NM_005477.3(HCN4):c.2328G>A (p.Pro776=) rs1452483960
NM_005477.3(HCN4):c.2346G>T (p.Leu782=)
NM_005477.3(HCN4):c.2349G>A (p.Gln783=) rs746658574
NM_005477.3(HCN4):c.2355C>T (p.Ala785=)
NM_005477.3(HCN4):c.2370T>C (p.Ser790=) rs747648596
NM_005477.3(HCN4):c.2382C>G (p.Ala794=) rs1399387925
NM_005477.3(HCN4):c.2385C>T (p.Leu795=) rs878854773
NM_005477.3(HCN4):c.2401C>T (p.Leu801=) rs898537235
NM_005477.3(HCN4):c.2409T>G (p.Ala803=)
NM_005477.3(HCN4):c.240G>C (p.Pro80=) rs747646946
NM_005477.3(HCN4):c.2420G>A (p.Arg807His) rs200395062
NM_005477.3(HCN4):c.2451C>T (p.Leu817=)
NM_005477.3(HCN4):c.2465C>T (p.Thr822Met) rs201143364
NM_005477.3(HCN4):c.2466G>A (p.Thr822=)
NM_005477.3(HCN4):c.246C>T (p.Arg82=) rs775895751
NM_005477.3(HCN4):c.2493C>A (p.Ser831=)
NM_005477.3(HCN4):c.2493C>T (p.Ser831=)
NM_005477.3(HCN4):c.2496G>T (p.Leu832=) rs139394937
NM_005477.3(HCN4):c.2508G>A (p.Ala836=) rs766293595
NM_005477.3(HCN4):c.2517C>T (p.Ser839=)
NM_005477.3(HCN4):c.2522C>T (p.Ser841Leu) rs200546024
NM_005477.3(HCN4):c.2523G>A (p.Ser841=) rs768157473
NM_005477.3(HCN4):c.2523G>T (p.Ser841=)
NM_005477.3(HCN4):c.2526C>T (p.Pro842=) rs201499694
NM_005477.3(HCN4):c.2537C>T (p.Pro846Leu) rs747467877
NM_005477.3(HCN4):c.2538G>A (p.Pro846=)
NM_005477.3(HCN4):c.2541C>G (p.Ser847=) rs772267234
NM_005477.3(HCN4):c.2595C>T (p.Phe865=)
NM_005477.3(HCN4):c.2604C>T (p.Pro868=) rs138773305
NM_005477.3(HCN4):c.2628C>T (p.Pro876=)
NM_005477.3(HCN4):c.2652C>T (p.Pro884=) rs373814254
NM_005477.3(HCN4):c.2668C>T (p.Pro890Ser) rs184801511
NM_005477.3(HCN4):c.2672C>T (p.Ser891Leu) rs768190354
NM_005477.3(HCN4):c.2694C>T (p.Gly898=) rs375169111
NM_005477.3(HCN4):c.2700C>T (p.Ala900=)
NM_005477.3(HCN4):c.2701G>A (p.Ala901Thr) rs201742383
NM_005477.3(HCN4):c.2715C>T (p.Ala905=) rs745886315
NM_005477.3(HCN4):c.2718G>A (p.Gly906=)
NM_005477.3(HCN4):c.2730C>A (p.Phe910Leu) rs200814534
NM_005477.3(HCN4):c.2733C>T (p.His911=) rs565795330
NM_005477.3(HCN4):c.2763C>T (p.Ser921=) rs764751378
NM_005477.3(HCN4):c.2781C>G (p.Thr927=)
NM_005477.3(HCN4):c.2784G>A (p.Pro928=)
NM_005477.3(HCN4):c.2796C>G (p.Gly932=)
NM_005477.3(HCN4):c.27C>G (p.Arg9=)
NM_005477.3(HCN4):c.2800C>T (p.Arg934Cys) rs199638465
NM_005477.3(HCN4):c.2804C>T (p.Ser935Phe) rs775803239
NM_005477.3(HCN4):c.2808G>A (p.Pro936=)
NM_005477.3(HCN4):c.2829C>T (p.Pro943=)
NM_005477.3(HCN4):c.2830G>A (p.Ala944Thr) rs777648103
NM_005477.3(HCN4):c.2832G>A (p.Ala944=)
NM_005477.3(HCN4):c.2845C>T (p.Arg949Trp) rs755614529
NM_005477.3(HCN4):c.2865G>A (p.Pro955=) rs1385591989
NM_005477.3(HCN4):c.2889C>T (p.Pro963=) rs1376847040
NM_005477.3(HCN4):c.2901C>T (p.Ser967=) rs570068696
NM_005477.3(HCN4):c.2904G>A (p.Pro968=) rs368145651
NM_005477.3(HCN4):c.2916C>T (p.Pro972=) rs559422705
NM_005477.3(HCN4):c.2922G>A (p.Gln974=)
NM_005477.3(HCN4):c.2937C>T (p.Pro979=)
NM_005477.3(HCN4):c.2949C>T (p.Ser983=)
NM_005477.3(HCN4):c.2967C>G (p.Gly989=)
NM_005477.3(HCN4):c.2978C>T (p.Thr993Met) rs199798661
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.3036G>C (p.Gly1012=) rs993764984
NM_005477.3(HCN4):c.3045C>T (p.Ser1015=) rs767495892
NM_005477.3(HCN4):c.3057T>C (p.Phe1019=)
NM_005477.3(HCN4):c.3075C>T (p.Leu1025=)
NM_005477.3(HCN4):c.3078C>T (p.Ser1026=) rs202188345
NM_005477.3(HCN4):c.3081C>T (p.Pro1027=)
NM_005477.3(HCN4):c.3087C>T (p.Gly1029=)
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.3135C>T (p.Ala1045=) rs1342751732
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.3195C>A (p.Val1065=) rs4493011
NM_005477.3(HCN4):c.3195C>T (p.Val1065=)
NM_005477.3(HCN4):c.321C>T (p.Gly107=) rs1555479019
NM_005477.3(HCN4):c.3228C>T (p.Pro1076=) rs770161577
NM_005477.3(HCN4):c.3261C>T (p.Ser1087=)
NM_005477.3(HCN4):c.3264G>A (p.Ala1088=) rs752705479
NM_005477.3(HCN4):c.3294G>A (p.Ala1098=) rs766077921
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.3396C>T (p.Ser1132=) rs369224427
NM_005477.3(HCN4):c.3405C>T (p.Leu1135=) rs548860628
NM_005477.3(HCN4):c.3411C>A (p.Pro1137=) rs763496884
NM_005477.3(HCN4):c.3417G>A (p.Gly1139=)
NM_005477.3(HCN4):c.3447C>T (p.His1149=)
NM_005477.3(HCN4):c.3468A>G (p.Thr1156=) rs947950341
NM_005477.3(HCN4):c.3531G>A (p.Gly1177=) rs375911378
NM_005477.3(HCN4):c.3531G>T (p.Gly1177=) rs375911378
NM_005477.3(HCN4):c.3579G>A (p.Glu1193=)
NM_005477.3(HCN4):c.3597G>A (p.Leu1199=)
NM_005477.3(HCN4):c.3600A>T (p.Pro1200=) rs529004
NM_005477.3(HCN4):c.375C>T (p.Ser125=)
NM_005477.3(HCN4):c.396C>A (p.Ile132=)
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.465C>T (p.Pro155=) rs956956393
NM_005477.3(HCN4):c.471C>T (p.Ala157=)
NM_005477.3(HCN4):c.513A>T (p.Pro171=)
NM_005477.3(HCN4):c.516G>A (p.Pro172=) rs772278008
NM_005477.3(HCN4):c.531C>T (p.Ala177=)
NM_005477.3(HCN4):c.546C>T (p.Pro182=)
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.579C>G (p.Gly193=)
NM_005477.3(HCN4):c.582G>A (p.Ala194=)
NM_005477.3(HCN4):c.585T>G (p.Ala195=) rs748468603
NM_005477.3(HCN4):c.588C>T (p.Ala196=)
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958
NM_005477.3(HCN4):c.633C>G (p.Ala211=)
NM_005477.3(HCN4):c.654C>T (p.Phe218=) rs764818507
NM_005477.3(HCN4):c.681C>T (p.Asn227=)
NM_005477.3(HCN4):c.691C>T (p.Leu231=)
NM_005477.3(HCN4):c.753A>G (p.Gly251=)
NM_005477.3(HCN4):c.771C>T (p.Pro257=)
NM_005477.3(HCN4):c.786-7T>C
NM_005477.3(HCN4):c.829C>T (p.Leu277=)
NM_005477.3(HCN4):c.852C>T (p.Ile284=)
NM_005477.3(HCN4):c.924C>T (p.Ile308=)
NM_005477.3(HCN4):c.954C>T (p.Ile318=) rs764050400
NM_005477.3(HCN4):c.972A>G (p.Thr324=) rs747884744
NM_005477.3(HCN4):c.984G>A (p.Leu328=)
NM_005477.3(HCN4):c.990G>A (p.Pro330=) rs146954200
NM_005477.3(HCN4):c.990G>T (p.Pro330=) rs146954200

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.