ClinVar Miner

Variants in gene HCN4 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 32
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_005477.3(HCN4):c.107G>A (p.Gly36Glu) rs143090627 0.04452
NM_005477.3(HCN4):c.1683C>A (p.Gly561=) rs62641690 0.01030
NM_005477.3(HCN4):c.3337A>G (p.Met1113Val) rs142735148 0.00983
NM_005477.3(HCN4):c.2648C>G (p.Pro883Arg) rs148398509 0.00737
NM_005477.3(HCN4):c.2657C>T (p.Ala886Val) rs200575377 0.00352
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
NM_005477.3(HCN4):c.3587G>A (p.Arg1196His) rs147181577 0.00191
NM_005477.3(HCN4):c.3350C>T (p.Pro1117Leu) rs140402087 0.00185
NM_005477.3(HCN4):c.1978+3G>T rs113112855 0.00166
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.1356C>T (p.Ser452=) rs148453034 0.00116
NM_005477.3(HCN4):c.2739G>A (p.Ala913=) rs373411041 0.00056
NM_005477.3(HCN4):c.2181C>T (p.His727=) rs140354126 0.00036
NM_005477.3(HCN4):c.1656C>T (p.His552=) rs148142070 0.00029
NM_005477.3(HCN4):c.1536C>T (p.His512=) rs146306966 0.00024
NM_005477.3(HCN4):c.2109C>T (p.Phe703=) rs150378994 0.00021
NM_005477.3(HCN4):c.2313C>T (p.Pro771=) rs142298104 0.00016
NM_005477.3(HCN4):c.1738-6C>T rs760763085 0.00014
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958 0.00012
NM_005477.3(HCN4):c.3117G>A (p.Pro1039=) rs749785521 0.00011
NM_005477.3(HCN4):c.3531G>T (p.Gly1177=) rs375911378 0.00008
NM_005477.3(HCN4):c.1243G>A (p.Val415Met) rs201978086 0.00007
NM_005477.3(HCN4):c.3009G>A (p.Pro1003=) rs775401682 0.00007
NM_005477.3(HCN4):c.1303C>T (p.Leu435=) rs746461789 0.00006
NM_005477.3(HCN4):c.2634C>G (p.Ser878=) rs748478312 0.00006
NM_005477.3(HCN4):c.1254C>T (p.Ile418=) rs373794941 0.00005
NM_005477.3(HCN4):c.1818C>T (p.Ser606=) rs1247778865 0.00002
NM_005477.3(HCN4):c.3264G>A (p.Ala1088=) rs752705479 0.00002
NM_005477.3(HCN4):c.1459G>A (p.Val487Met) rs202037304 0.00001
NM_005477.3(HCN4):c.2055C>T (p.Ser685=) rs886042819 0.00001
NM_005477.3(HCN4):c.785+18T>A rs1412056222

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.