ClinVar Miner

List of variants in gene HCN4 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
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.36C>G (p.Leu12=) rs201193660 0.00635
NM_005477.3(HCN4):c.2275G>A (p.Val759Ile) rs62641689 0.00258
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.*2581C>T rs535089156 0.00083
NM_005477.3(HCN4):c.*1085A>C rs563333401 0.00036
NM_005477.3(HCN4):c.621C>G (p.Arg207=) rs727503958 0.00012
NM_005477.3(HCN4):c.1303C>T (p.Leu435=) rs746461789 0.00006
NM_005477.3(HCN4):c.1455G>A (p.Ala485=) rs148875639 0.00004
NM_005477.3(HCN4):c.2715C>T (p.Ala905=) rs745886315 0.00004
NM_005477.3(HCN4):c.3209G>A (p.Gly1070Asp) rs772839442 0.00004
NM_005477.3(HCN4):c.497C>T (p.Pro166Leu) rs771442346 0.00004
NM_005477.3(HCN4):c.3293C>T (p.Ala1098Val) rs1064797200 0.00003
NM_005477.3(HCN4):c.2309C>A (p.Thr770Lys) rs763021264
NM_005477.3(HCN4):c.2494C>T (p.Leu832=)
NM_005477.3(HCN4):c.3105A>C (p.Pro1035=)
NM_005477.3(HCN4):c.3300T>C (p.Thr1100=) rs2151213924

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.