ClinVar Miner

List of variants in gene DEPDC5 studied for not provided

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Gene type:
ClinVar version:
Total variants: 148
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HGVS dbSNP
GRCh37/hg19 22q12.2(chr22:32150908-32156688)x1
GRCh37/hg19 22q12.2(chr22:32164800-32164849)x1
NM_001242896.1:c.2958_2959insAlu
NM_001242896.3(DEPDC5):c.1119G>A (p.Pro373=) rs779115990
NM_001242896.3(DEPDC5):c.132C>T (p.Pro44=) rs1601581899
NM_001242896.3(DEPDC5):c.1353C>T (p.Asn451=) rs377336412
NM_001242896.3(DEPDC5):c.1398G>A (p.Val466=) rs1602054069
NM_001242896.3(DEPDC5):c.1403G>A (p.Arg468Lys)
NM_001242896.3(DEPDC5):c.1550_1565dup (p.Asp522delinsGluGluProGlyPheTer)
NM_001242896.3(DEPDC5):c.1667-4G>A rs1290733834
NM_001242896.3(DEPDC5):c.191del (p.Lys64fs) rs1601599644
NM_001242896.3(DEPDC5):c.1926G>A (p.Glu642=) rs1602157090
NM_001242896.3(DEPDC5):c.2088T>C (p.Leu696=) rs1392957764
NM_001242896.3(DEPDC5):c.2104+10C>G rs779221302
NM_001242896.3(DEPDC5):c.2121C>T (p.Thr707=) rs1602267687
NM_001242896.3(DEPDC5):c.2178A>G (p.Thr726=) rs559312468
NM_001242896.3(DEPDC5):c.2187T>C (p.Ala729=) rs1395354365
NM_001242896.3(DEPDC5):c.232del (p.Arg78fs)
NM_001242896.3(DEPDC5):c.2349C>T (p.Ile783=) rs771501558
NM_001242896.3(DEPDC5):c.2358G>A (p.Arg786=) rs1462755261
NM_001242896.3(DEPDC5):c.2413del (p.Gln805fs)
NM_001242896.3(DEPDC5):c.2466C>A (p.Pro822=) rs770266753
NM_001242896.3(DEPDC5):c.2500C>G (p.Pro834Ala) rs1569067813
NM_001242896.3(DEPDC5):c.2633+7A>G rs1169099672
NM_001242896.3(DEPDC5):c.2634-5del rs1602354182
NM_001242896.3(DEPDC5):c.274C>T (p.Pro92Ser) rs774294197
NM_001242896.3(DEPDC5):c.2844G>C (p.Leu948=) rs151215663
NM_001242896.3(DEPDC5):c.2853C>T (p.Ala951=) rs1602367039
NM_001242896.3(DEPDC5):c.3003C>A (p.Arg1001=) rs1602368616
NM_001242896.3(DEPDC5):c.3030C>T (p.Thr1010=) rs548885626
NM_001242896.3(DEPDC5):c.3213C>T (p.Ala1071=) rs373166302
NM_001242896.3(DEPDC5):c.3321C>T (p.Phe1107=) rs752465449
NM_001242896.3(DEPDC5):c.3456C>T (p.Gly1152=) rs757188110
NM_001242896.3(DEPDC5):c.3622G>A (p.Ala1208Thr) rs748662185
NM_001242896.3(DEPDC5):c.363+10G>C rs562677392
NM_001242896.3(DEPDC5):c.3816G>A (p.Gln1272=) rs1602677099
NM_001242896.3(DEPDC5):c.3948G>C (p.Leu1316=) rs371864100
NM_001242896.3(DEPDC5):c.3973del (p.Ser1325fs)
NM_001242896.3(DEPDC5):c.4125T>C (p.His1375=) rs200220521
NM_001242896.3(DEPDC5):c.4197dup (p.Glu1400fs)
NM_001242896.3(DEPDC5):c.4283G>A (p.Ser1428Asn)
NM_001242896.3(DEPDC5):c.4531C>T (p.Leu1511=) rs769593405
NM_001242896.3(DEPDC5):c.4767G>A (p.Thr1589=) rs1023748508
NM_001242896.3(DEPDC5):c.483+8T>G rs1363426695
NM_001242896.3(DEPDC5):c.504G>A (p.Ser168=)
NM_001242896.3(DEPDC5):c.944_945del (p.Asn315fs) rs1601935630
NM_001242896.3(DEPDC5):c.946+5G>T
NM_001242896.3(DEPDC5):c.946+7A>G rs1184606889
NM_001242896.3(DEPDC5):c.999_1000del (p.Val334fs) rs1601969933
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.1095T>C (p.Asp365=) rs79070552
NM_001242897.2(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310
NM_001242897.2(DEPDC5):c.1165C>T (p.Arg389Cys) rs41311139
NM_001242897.2(DEPDC5):c.1184A>C (p.Asp395Ala) rs1064796205
NM_001242897.2(DEPDC5):c.1226C>G (p.Thr409Arg) rs773704927
NM_001242897.2(DEPDC5):c.1230C>G (p.Ser410=) rs771613005
NM_001242897.2(DEPDC5):c.1247G>T (p.Cys416Phe) rs767747105
NM_001242897.2(DEPDC5):c.1265G>A (p.Arg422Gln) rs886039277
NM_001242897.2(DEPDC5):c.1290C>T (p.Pro430=) rs201202102
NM_001242897.2(DEPDC5):c.130C>G (p.Pro44Ala) rs756878843
NM_001242897.2(DEPDC5):c.1330G>A (p.Gly444Arg) rs201394709
NM_001242897.2(DEPDC5):c.138T>A (p.Asp46Glu) rs535630975
NM_001242897.2(DEPDC5):c.1412G>A (p.Gly471Asp) rs1351408059
NM_001242897.2(DEPDC5):c.1416A>G (p.Pro472=) rs930376201
NM_001242897.2(DEPDC5):c.1453C>T (p.Arg485Ter) rs1568991466
NM_001242897.2(DEPDC5):c.1459C>T (p.Arg487Ter) rs587777459
NM_001242897.2(DEPDC5):c.1474C>T (p.Arg492Ter) rs1057519107
NM_001242897.2(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639
NM_001242897.2(DEPDC5):c.1526G>A (p.Arg509His) rs372489331
NM_001242897.2(DEPDC5):c.1555C>T (p.Gln519Ter) rs886039261
NM_001242897.2(DEPDC5):c.1604T>C (p.Ile535Thr) rs1171016858
NM_001242897.2(DEPDC5):c.161A>C (p.Gln54Pro) rs201312113
NM_001242897.2(DEPDC5):c.1663C>T (p.Arg555Ter) rs587776973
NM_001242897.2(DEPDC5):c.1666G>A (p.Asp556Asn) rs1064795160
NM_001242897.2(DEPDC5):c.1759C>T (p.Arg587Ter) rs886039263
NM_001242897.2(DEPDC5):c.1870+10T>C rs760092505
NM_001242897.2(DEPDC5):c.1870+2304A>G rs1064794610
NM_001242897.2(DEPDC5):c.1870+2315C>T rs780960812
NM_001242897.2(DEPDC5):c.1870+2328C>T rs16989528
NM_001242897.2(DEPDC5):c.1870+2364dup rs1475605360
NM_001242897.2(DEPDC5):c.1870+2399G>A rs753762209
NM_001242897.2(DEPDC5):c.1870+3481C>T rs181347577
NM_001242897.2(DEPDC5):c.1870+3516C>A rs61731667
NM_001242897.2(DEPDC5):c.1870+3527A>C rs370940232
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.1937-9G>A rs770492339
NM_001242897.2(DEPDC5):c.196A>T (p.Thr66Ser) rs1556523682
NM_001242897.2(DEPDC5):c.2019G>A (p.Ala673=) rs777616535
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.2127C>T (p.Asp709=) rs371165640
NM_001242897.2(DEPDC5):c.2182C>T (p.Arg728Cys) rs953743301
NM_001242897.2(DEPDC5):c.2247G>A (p.Pro749=) rs61731664
NM_001242897.2(DEPDC5):c.2287G>A (p.Val763Met) rs1555899402
NM_001242897.2(DEPDC5):c.2567+8A>G rs370009456
NM_001242897.2(DEPDC5):c.2622T>C (p.Cys874=) rs115299174
NM_001242897.2(DEPDC5):c.2645C>T (p.Thr882Met) rs1064795107
NM_001242897.2(DEPDC5):c.2646G>A (p.Thr882=) rs767693306
NM_001242897.2(DEPDC5):c.2739G>A (p.Glu913=) rs370906184
NM_001242897.2(DEPDC5):c.2851A>G (p.Thr951Ala) rs537257402
NM_001242897.2(DEPDC5):c.28G>A (p.Val10Ile) rs375027042
NM_001242897.2(DEPDC5):c.2979C>G (p.Ala993=) rs373166302
NM_001242897.2(DEPDC5):c.3007A>C (p.Thr1003Pro) rs142540948
NM_001242897.2(DEPDC5):c.3025C>T (p.Arg1009Ter) rs587777458
NM_001242897.2(DEPDC5):c.3030+3822C>T rs772812141
NM_001242897.2(DEPDC5):c.3030+3879A>G rs1555909576
NM_001242897.2(DEPDC5):c.3031-10del rs377356885
NM_001242897.2(DEPDC5):c.3058A>G (p.Met1020Val) rs61731662
NM_001242897.2(DEPDC5):c.3161C>T (p.Ser1054Phe) rs578244490
NM_001242897.2(DEPDC5):c.3186-5dup rs1555914747
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.351A>G (p.Leu117=) rs746535603
NM_001242897.2(DEPDC5):c.363+6_363+7del rs748242785
NM_001242897.2(DEPDC5):c.3678G>T (p.Arg1226Ser) rs374647774
NM_001242897.2(DEPDC5):c.3797G>A (p.Arg1266Gln) rs1064795095
NM_001242897.2(DEPDC5):c.3797G>T (p.Arg1266Leu) rs1064795095
NM_001242897.2(DEPDC5):c.380A>G (p.Tyr127Cys) rs370881336
NM_001242897.2(DEPDC5):c.388C>T (p.Gln130Ter) rs1569512941
NM_001242897.2(DEPDC5):c.4002C>G (p.Pro1334=) rs531253840
NM_001242897.2(DEPDC5):c.4076G>A (p.Ser1359Asn) rs1245607244
NM_001242897.2(DEPDC5):c.4091C>T (p.Thr1364Met) rs556147064
NM_001242897.2(DEPDC5):c.4108C>T (p.His1370Tyr) rs1064795311
NM_001242897.2(DEPDC5):c.413+7A>G rs1057519230
NM_001242897.2(DEPDC5):c.414-9T>G rs1556556448
NM_001242897.2(DEPDC5):c.4204T>C (p.Tyr1402His) rs1064796662
NM_001242897.2(DEPDC5):c.4212C>T (p.His1404=) rs146449468
NM_001242897.2(DEPDC5):c.4219+1G>A rs1555942720
NM_001242897.2(DEPDC5):c.4220-12C>T rs1603016321
NM_001242897.2(DEPDC5):c.4271A>G (p.Gln1424Arg) rs377585542
NM_001242897.2(DEPDC5):c.4292C>T (p.Thr1431Ile) rs1064794532
NM_001242897.2(DEPDC5):c.4493T>C (p.Met1498Thr) rs1555943470
NM_001242897.2(DEPDC5):c.501G>A (p.Thr167=) rs766360619
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.814G>A (p.Val272Ile) rs187334123
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

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