ClinVar Miner

List of variants in gene DEPDC5 reported as benign for central nervous system disorder

Included ClinVar conditions (2498):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 62
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001242896.3(DEPDC5):c.484-43G>C rs138286 0.97589
NM_001242896.3(DEPDC5):c.1666+214A>C rs5749334 0.62803
NM_001242896.3(DEPDC5):c.1323A>C (p.Thr441=) rs5998135 0.11421
NM_001242896.3(DEPDC5):c.2170+11G>A rs55645350 0.10718
NM_001242896.3(DEPDC5):c.1472G>C (p.Ser491Thr) rs8138516 0.03859
NM_001242896.3(DEPDC5):c.885A>G (p.Gln295=) rs16989495 0.03316
NM_001242896.3(DEPDC5):c.364-10C>T rs116263417 0.03313
NM_001242896.3(DEPDC5):c.1922C>T (p.Ala641Val) rs16989528 0.02752
NM_001242896.3(DEPDC5):c.1095T>C (p.Asp365=) rs79070552 0.02578
NM_001242896.3(DEPDC5):c.2241C>G (p.Leu747=) rs16989537 0.02410
NM_001242896.3(DEPDC5):c.2135C>T (p.Ser712Phe) rs16989535 0.02396
NM_001242896.3(DEPDC5):c.3358A>G (p.Met1120Val) rs61731662 0.02356
NM_001242896.3(DEPDC5):c.1165C>T (p.Arg389Cys) rs41311139 0.01988
NM_001242896.3(DEPDC5):c.4512C>T (p.His1504=) rs146449468 0.01383
NM_001242896.3(DEPDC5):c.2481G>A (p.Pro827=) rs61731664 0.01330
NM_001242896.3(DEPDC5):c.3696+18G>A rs9621356 0.01290
NM_001242896.3(DEPDC5):c.2742G>A (p.Glu914=) rs118001924 0.01176
NM_001242896.3(DEPDC5):c.2139A>G (p.Leu713=) rs16989536 0.00675
NM_001242896.3(DEPDC5):c.2856T>C (p.Cys952=) rs115299174 0.00386
NM_001242896.3(DEPDC5):c.3810C>T (p.Ala1270=) rs200033252 0.00252
NM_001242896.3(DEPDC5):c.2072T>C (p.Leu691Pro) rs201464790 0.00227
NM_001242896.3(DEPDC5):c.2075C>T (p.Ser692Phe) rs199783404 0.00227
NM_001242896.3(DEPDC5):c.2020C>T (p.Arg674Cys) rs181347577 0.00218
NM_001242896.3(DEPDC5):c.2801+8A>G rs370009456 0.00206
NM_001242896.3(DEPDC5):c.3683T>C (p.Ile1228Thr) rs200653339 0.00200
NM_001242896.3(DEPDC5):c.4519+13G>A rs181976978 0.00193
NM_001242896.3(DEPDC5):c.814G>A (p.Val272Ile) rs187334123 0.00167
NM_001242896.3(DEPDC5):c.1615C>G (p.His539Asp) rs193042481 0.00082
NM_001242896.3(DEPDC5):c.3567A>G (p.Thr1189=) rs142197878 0.00063
NM_001242896.3(DEPDC5):c.624+13_624+14del rs777746872 0.00059
NM_001242896.3(DEPDC5):c.3092C>A (p.Pro1031His) rs376744360 0.00041
NM_001242896.3(DEPDC5):c.1389C>T (p.Asp463=) rs188147862 0.00039
NM_001242896.3(DEPDC5):c.3342C>T (p.Asp1114=) rs774805884 0.00037
NM_001242896.3(DEPDC5):c.193+12A>G rs376099179 0.00029
NM_001242896.3(DEPDC5):c.957G>A (p.Lys319=) rs545689068 0.00026
NM_001242896.3(DEPDC5):c.1355C>T (p.Ala452Val) rs202226316 0.00020
NM_001242896.3(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113 0.00019
NM_001242896.3(DEPDC5):c.3331-19A>G rs377292271 0.00019
NM_001242896.3(DEPDC5):c.3643G>A (p.Val1215Met) rs201603222 0.00019
NM_001242896.3(DEPDC5):c.4764C>T (p.Val1588=) rs540471738 0.00007
NM_001242896.3(DEPDC5):c.562+13T>C rs773199371 0.00004
NM_001242896.3(DEPDC5):c.2004A>G (p.Gly668=) rs374037144 0.00003
NM_001242896.3(DEPDC5):c.4125T>C (p.His1375=) rs200220521 0.00003
NM_001242896.3(DEPDC5):c.2171-15dup rs765158089 0.00002
NM_001242896.3(DEPDC5):c.2286C>T (p.Asp762=) rs200465447 0.00002
NM_001242896.3(DEPDC5):c.3099G>C (p.Val1033=) rs776701394 0.00001
NM_001242896.3(DEPDC5):c.3195G>A (p.Lys1065=) rs769742063 0.00001
NM_001242896.3(DEPDC5):c.4302C>G (p.Pro1434=) rs531253840 0.00001
NM_001242896.3(DEPDC5):c.1082-3dup rs766994249
NM_001242896.3(DEPDC5):c.1218-13_1218-10del rs150103661
NM_001242896.3(DEPDC5):c.1218-5del rs758572377
NM_001242896.3(DEPDC5):c.1324+25dup
NM_001242896.3(DEPDC5):c.2055C>A (p.Phe685Leu) rs61731667
NM_001242896.3(DEPDC5):c.2516-8dup
NM_001242896.3(DEPDC5):c.2634-5del rs1602354182
NM_001242896.3(DEPDC5):c.3213C>T (p.Ala1071=) rs373166302
NM_001242896.3(DEPDC5):c.363+19del rs529780938
NM_001242896.3(DEPDC5):c.363+19dup rs529780938
NM_001242896.3(DEPDC5):c.4437-15C>G rs755374231
NM_001242896.3(DEPDC5):c.483+15del
NM_001242896.3(DEPDC5):c.562+8_562+9del rs754265066
NM_001242896.3(DEPDC5):c.946+17G>A

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.