ClinVar Miner

List of variants in gene TRDN reported as likely pathogenic for catecholaminergic polymorphic ventricular tachycardia 5

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_006073.4(TRDN):c.1282C>T (p.Arg428Ter) rs202219343 0.00016
NM_006073.4(TRDN):c.1420+1G>T rs1375657667 0.00003
NM_006073.4(TRDN):c.1050del (p.Glu351fs) rs753514580
NM_006073.4(TRDN):c.1051+1G>A rs535908547
NM_006073.4(TRDN):c.1233_1234dup (p.Lys412fs) rs778198100
NM_006073.4(TRDN):c.1558G>T (p.Glu520Ter)
NM_006073.4(TRDN):c.1806del (p.Gly603fs) rs1381728472
NM_006073.4(TRDN):c.391+1G>A rs2114436209
NM_006073.4(TRDN):c.424+1G>T
NM_006073.4(TRDN):c.531del (p.Glu178fs) rs1432170970
NM_006073.4(TRDN):c.568dup (p.Ile190fs) rs1085307100

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.