ClinVar Miner

List of variants in gene DEPDC5 reported as uncertain significance by CeGaT Praxis fuer Humangenetik Tuebingen

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
HGVS dbSNP
NM_001242897.2(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310
NM_001242897.2(DEPDC5):c.1226C>G (p.Thr409Arg) rs773704927
NM_001242897.2(DEPDC5):c.1290C>T (p.Pro430=) rs201202102
NM_001242897.2(DEPDC5):c.1604T>C (p.Ile535Thr) rs1171016858
NM_001242897.2(DEPDC5):c.196A>T (p.Thr66Ser) rs1556523682
NM_001242897.2(DEPDC5):c.2052C>T (p.Asp684=) rs200465447
NM_001242897.2(DEPDC5):c.2066A>C (p.Gln689Pro) rs1057519238
NM_001242897.2(DEPDC5):c.2739G>A (p.Glu913=) rs370906184
NM_001242897.2(DEPDC5):c.3797G>A (p.Arg1266Gln) rs1064795095
NM_001242897.2(DEPDC5):c.4076G>A (p.Ser1359Asn) rs1245607244
NM_001242897.2(DEPDC5):c.413+7A>G rs1057519230
NM_001242897.2(DEPDC5):c.501G>A (p.Thr167=) rs766360619

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.