ClinVar Miner

List of variants in gene combination HCN4, LOC105370890, LOC126862173 reported as likely benign for Brugada syndrome 8

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 44
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HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.1090G>A (p.Asp364Asn) rs151004999 0.00029
NM_005477.3(HCN4):c.1014G>C (p.Leu338=) rs147771899 0.00024
NM_005477.3(HCN4):c.1089C>T (p.Ile363=) rs140902511 0.00015
NM_005477.3(HCN4):c.990G>A (p.Pro330=) rs146954200 0.00007
NM_005477.3(HCN4):c.954C>T (p.Ile318=) rs764050400 0.00003
NM_005477.3(HCN4):c.1053C>T (p.Pro351=) rs773287506 0.00002
NM_005477.3(HCN4):c.1140G>A (p.Thr380=) rs370059727 0.00002
NM_005477.3(HCN4):c.786-4G>A rs757807007 0.00002
NM_005477.3(HCN4):c.924C>T (p.Ile308=) rs1256500370 0.00002
NM_005477.3(HCN4):c.1027A>G (p.Met343Val) rs185719200 0.00001
NM_005477.3(HCN4):c.1095G>A (p.Ser365=) rs778276793 0.00001
NM_005477.3(HCN4):c.1162C>T (p.Leu388=) rs1158045945 0.00001
NM_005477.3(HCN4):c.829C>T (p.Leu277=) rs1334334457 0.00001
NM_005477.3(HCN4):c.864G>A (p.Lys288=) rs1296638967 0.00001
NM_005477.3(HCN4):c.972A>G (p.Thr324=) rs747884744 0.00001
NM_005477.3(HCN4):c.1008G>A (p.Lys336=)
NM_005477.3(HCN4):c.1020C>T (p.Ser340=)
NM_005477.3(HCN4):c.1038C>T (p.Phe346=)
NM_005477.3(HCN4):c.1044C>G (p.Ser348=) rs2151221193
NM_005477.3(HCN4):c.1044C>T (p.Ser348=)
NM_005477.3(HCN4):c.1120C>T (p.Leu374=) rs779213932
NM_005477.3(HCN4):c.1137C>T (p.Phe379=)
NM_005477.3(HCN4):c.786-10C>T
NM_005477.3(HCN4):c.786-15del
NM_005477.3(HCN4):c.786-16_786-15del rs1479279626
NM_005477.3(HCN4):c.786-18C>G
NM_005477.3(HCN4):c.786-7T>C rs2151221269
NM_005477.3(HCN4):c.813G>A (p.Leu271=)
NM_005477.3(HCN4):c.822G>A (p.Val274=)
NM_005477.3(HCN4):c.822G>T (p.Val274=)
NM_005477.3(HCN4):c.852C>T (p.Ile284=) rs2151221261
NM_005477.3(HCN4):c.855C>G (p.Thr285=)
NM_005477.3(HCN4):c.858C>T (p.Phe286=)
NM_005477.3(HCN4):c.882C>G (p.Pro294=)
NM_005477.3(HCN4):c.900G>T (p.Val300=)
NM_005477.3(HCN4):c.903G>A (p.Val301=)
NM_005477.3(HCN4):c.918C>T (p.Phe306=)
NM_005477.3(HCN4):c.921C>T (p.Leu307=) rs2151221238
NM_005477.3(HCN4):c.928T>C (p.Leu310=)
NM_005477.3(HCN4):c.933C>T (p.Val311=)
NM_005477.3(HCN4):c.957G>A (p.Val319=)
NM_005477.3(HCN4):c.984G>A (p.Leu328=) rs1030745095
NM_005477.3(HCN4):c.990G>C (p.Pro330=) rs146954200
NM_005477.3(HCN4):c.990G>T (p.Pro330=) rs146954200

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