ClinVar Miner

List of variants in gene DEPDC5 reported as uncertain significance for Seizures

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 19
Download table as spreadsheet
HGVS dbSNP
NM_001242897.2(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310
NM_001242897.2(DEPDC5):c.1246T>C (p.Cys416Arg) rs1568962734
NM_001242897.2(DEPDC5):c.1291G>T (p.Ala431Ser)
NM_001242897.2(DEPDC5):c.146+5G>A rs748264035
NM_001242897.2(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639
NM_001242897.2(DEPDC5):c.1870+3487C>G
NM_001242897.2(DEPDC5):c.2009C>G (p.Thr670Ser) rs1569060315
NM_001242897.2(DEPDC5):c.2357C>T (p.Thr786Met) rs564667614
NM_001242897.2(DEPDC5):c.262A>G (p.Asn88Asp) rs144712084
NM_001242897.2(DEPDC5):c.3030+3861C>T rs79027628
NM_001242897.2(DEPDC5):c.3378G>A (p.Met1126Ile)
NM_001242897.2(DEPDC5):c.3571C>T (p.Arg1191Cys)
NM_001242897.2(DEPDC5):c.3826G>A (p.Gly1276Ser) rs1555929990
NM_001242897.2(DEPDC5):c.3856A>C (p.Ile1286Leu) rs1555930038
NM_001242897.2(DEPDC5):c.3903+5G>A rs1569224557
NM_001242897.2(DEPDC5):c.4439G>A (p.Cys1480Tyr)
NM_001242897.2(DEPDC5):c.842A>T (p.Tyr281Phe) rs200797928
NM_001242897.2(DEPDC5):c.944A>G (p.Asn315Ser)
NM_001242897.2(DEPDC5):c.968A>G (p.Asn323Ser) rs201776005

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.