ClinVar Miner

List of variants in gene CYCS reported by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018947.6(CYCS):c.*4524del rs754793722 0.00130
NM_018947.6(CYCS):c.*5013T>C rs759244161 0.00048
NM_018947.6(CYCS):c.*1622del rs199806702 0.00021
NM_018947.6(CYCS):c.147C>T (p.Tyr49=) rs375916000 0.00004
NM_018947.6(CYCS):c.*1676_*1678dup rs11427893
NM_018947.6(CYCS):c.*1678dup rs11427893
NM_018947.6(CYCS):c.*1702_*1705dup rs141609926
NM_018947.6(CYCS):c.*1839C>T rs886062249
NM_018947.6(CYCS):c.*2563_*2564del rs886062242
NM_018947.6(CYCS):c.*3282del rs536451231
NM_018947.6(CYCS):c.*3610del rs60346464
NM_018947.6(CYCS):c.*4723_*4725del rs113653188
NM_018947.6(CYCS):c.*5004_*5005del rs527409336

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.