ClinVar Miner

List of variants in gene DEPDC5 reported as likely pathogenic for not provided

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP
GRCh37/hg19 22q12.2(chr22:32150908-32156688)x1
GRCh37/hg19 22q12.2(chr22:32164800-32164849)x1
NM_001242896.3(DEPDC5):c.1550_1565dup (p.Asp522delinsGluGluProGlyPheTer)
NM_001242896.3(DEPDC5):c.2413del (p.Gln805fs)
NM_001242896.3(DEPDC5):c.944_945del (p.Asn315fs) rs1601935630
NM_001242896.3(DEPDC5):c.999_1000del (p.Val334fs) rs1601969933
NM_001242897.2(DEPDC5):c.1474C>T (p.Arg492Ter) rs1057519107
NM_001242897.2(DEPDC5):c.1870+2315C>T rs780960812
NM_001242897.2(DEPDC5):c.1870+2364dup rs1475605360
NM_001242897.2(DEPDC5):c.3262_3263dup (p.Thr1089fs) rs1555914806
NM_001242897.2(DEPDC5):c.388C>T (p.Gln130Ter) rs1569512941
NM_001242897.2(DEPDC5):c.4219+1G>A rs1555942720
NM_001242897.2(DEPDC5):c.562+1G>A rs1057524233
NM_001242897.2(DEPDC5):c.58+5G>C rs1064794917
NM_001242897.2(DEPDC5):c.946+1G>A rs1556608580

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.