ClinVar Miner

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

Included ClinVar conditions (23):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP
NM_005477.2(HCN4):c.1243G>A (p.Val415Met) rs201978086
NM_005477.2(HCN4):c.1356C>T (p.Ser452=) rs148453034
NM_005477.2(HCN4):c.1371+8C>T rs199838832
NM_005477.2(HCN4):c.1371+9G>A rs200303699
NM_005477.2(HCN4):c.1459G>A (p.Val487Met) rs202037304
NM_005477.2(HCN4):c.1518C>T (p.Tyr506=) rs139590882
NM_005477.2(HCN4):c.1536C>T (p.His512=) rs146306966
NM_005477.2(HCN4):c.1653C>A (p.Ile551=) rs141966309
NM_005477.2(HCN4):c.1683C>A (p.Gly561=) rs62641690
NM_005477.2(HCN4):c.1839C>T (p.Phe613=) rs117731813
NM_005477.2(HCN4):c.1978+3G>T rs113112855
NM_005477.2(HCN4):c.2275G>A (p.Val759Ile) rs62641689
NM_005477.2(HCN4):c.2556G>A (p.Pro852=) rs117819825
NM_005477.2(HCN4):c.2601C>A (p.Ala867=) rs143188160
NM_005477.2(HCN4):c.2648C>G (p.Pro883Arg) rs148398509
NM_005477.2(HCN4):c.2657C>T (p.Ala886Val) rs200575377
NM_005477.2(HCN4):c.2673G>A (p.Ser891=) rs191092709
NM_005477.2(HCN4):c.2700C>A (p.Ala900=) rs377656260
NM_005477.2(HCN4):c.2739G>A (p.Ala913=) rs373411041
NM_005477.2(HCN4):c.2831C>T (p.Ala944Val) rs144450232
NM_005477.2(HCN4):c.2979G>A (p.Thr993=) rs75307879
NM_005477.2(HCN4):c.3033T>G (p.Ser1011=) rs186728422
NM_005477.2(HCN4):c.3288C>T (p.Asp1096=) rs116042117
NM_005477.2(HCN4):c.3337A>G (p.Met1113Val) rs142735148
NM_005477.2(HCN4):c.3350C>T (p.Pro1117Leu) rs140402087
NM_005477.2(HCN4):c.3577G>C (p.Glu1193Gln) rs200507617
NM_005477.2(HCN4):c.3587G>A (p.Arg1196His) rs147181577
NM_005477.2(HCN4):c.36C>G (p.Leu12=) rs201193660
NM_005477.2(HCN4):c.546C>G (p.Pro182=) rs571671463

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