ClinVar Miner

List of variants in gene DEPDC5 reported by GeneDx

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 46
Download table as spreadsheet
HGVS dbSNP
NM_001242897.2(DEPDC5):c.1010C>T (p.Thr337Met) rs1037878155
NM_001242897.2(DEPDC5):c.1045C>T (p.Leu349Phe) rs1085307532
NM_001242897.2(DEPDC5):c.1184A>C (p.Asp395Ala) rs1064796205
NM_001242897.2(DEPDC5):c.1247G>T (p.Cys416Phe) rs767747105
NM_001242897.2(DEPDC5):c.1412G>A (p.Gly471Asp) rs1351408059
NM_001242897.2(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639
NM_001242897.2(DEPDC5):c.1555C>T (p.Gln519Ter) rs886039261
NM_001242897.2(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113
NM_001242897.2(DEPDC5):c.1666G>A (p.Asp556Asn) rs1064795160
NM_001242897.2(DEPDC5):c.1870+2304A>G rs1064794610
NM_001242897.2(DEPDC5):c.1870+2315C>T rs780960812
NM_001242897.2(DEPDC5):c.1870+2364dup rs1475605360
NM_001242897.2(DEPDC5):c.1870+2399G>A rs753762209
NM_001242897.2(DEPDC5):c.1883G>T (p.Arg628Met) rs1064795377
NM_001242897.2(DEPDC5):c.1903C>A (p.Leu635Ile) rs1555894264
NM_001242897.2(DEPDC5):c.194-5T>C rs752848631
NM_001242897.2(DEPDC5):c.2287G>A (p.Val763Met) rs1555899402
NM_001242897.2(DEPDC5):c.2645C>T (p.Thr882Met) rs1064795107
NM_001242897.2(DEPDC5):c.28G>A (p.Val10Ile) rs375027042
NM_001242897.2(DEPDC5):c.3030+3879A>G rs1555909576
NM_001242897.2(DEPDC5):c.3262_3263dup (p.Thr1089fs) rs1555914806
NM_001242897.2(DEPDC5):c.336_337del (p.Asp113fs) rs1085307452
NM_001242897.2(DEPDC5):c.3391A>G (p.Met1131Val) rs1064796392
NM_001242897.2(DEPDC5):c.3678G>T (p.Arg1226Ser) rs374647774
NM_001242897.2(DEPDC5):c.3797G>T (p.Arg1266Leu) rs1064795095
NM_001242897.2(DEPDC5):c.388C>T (p.Gln130Ter) rs1569512941
NM_001242897.2(DEPDC5):c.4108C>T (p.His1370Tyr) rs1064795311
NM_001242897.2(DEPDC5):c.4137G>A (p.Arg1379=) rs1057522689
NM_001242897.2(DEPDC5):c.414-9T>G rs1556556448
NM_001242897.2(DEPDC5):c.4204T>C (p.Tyr1402His) rs1064796662
NM_001242897.2(DEPDC5):c.4213G>A (p.Val1405Ile) rs1057518240
NM_001242897.2(DEPDC5):c.4220-12C>T
NM_001242897.2(DEPDC5):c.4292C>T (p.Thr1431Ile) rs1064794532
NM_001242897.2(DEPDC5):c.4294A>G (p.Ser1432Gly) rs752046892
NM_001242897.2(DEPDC5):c.4493T>C (p.Met1498Thr) rs1555943470
NM_001242897.2(DEPDC5):c.562+1G>A rs1057524233
NM_001242897.2(DEPDC5):c.58+5G>C rs1064794917
NM_001242897.2(DEPDC5):c.59-3C>G rs1064795947
NM_001242897.2(DEPDC5):c.638G>C (p.Ser213Thr) rs374290113
NM_001242897.2(DEPDC5):c.715C>T (p.Arg239Ter) rs587776976
NM_001242897.2(DEPDC5):c.752A>G (p.Tyr251Cys) rs1064796158
NM_001242897.2(DEPDC5):c.842A>T (p.Tyr281Phe) rs200797928
NM_001242897.2(DEPDC5):c.856C>T (p.Arg286Ter) rs886039255
NM_001242897.2(DEPDC5):c.946+1G>A rs1556608580
NM_001242897.2(DEPDC5):c.953A>G (p.Asp318Gly) rs1064795102
NM_001242897.2(DEPDC5):c.983G>C (p.Arg328Pro) rs775605247

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.