ClinVar Miner

List of variants in gene DEPDC5 reported as uncertain significance for Familial focal epilepsy with variable foci

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 199
Download table as spreadsheet
HGVS dbSNP
NC_000022.10:g.(?_32253411)_(32302503_?)dup
NC_000022.10:g.(?_32297708)_(32302503_?)dup
NC_000022.11:g.(?_31798562)_(31798676_?)del
NC_000022.11:g.(?_31893562)_(31897673_?)del
NM_001242896.3(DEPDC5):c.1074A>G (p.Ile358Met)
NM_001242896.3(DEPDC5):c.1082-3T>A
NM_001242896.3(DEPDC5):c.1160C>T (p.Ala387Val)
NM_001242896.3(DEPDC5):c.1217+8C>A
NM_001242896.3(DEPDC5):c.1253G>T (p.Ser418Ile)
NM_001242896.3(DEPDC5):c.1456G>A (p.Glu486Lys)
NM_001242896.3(DEPDC5):c.1475G>A (p.Arg492Gln)
NM_001242896.3(DEPDC5):c.1489T>C (p.Ser497Pro)
NM_001242896.3(DEPDC5):c.1609C>T (p.His537Tyr)
NM_001242896.3(DEPDC5):c.1640G>C (p.Ser547Thr)
NM_001242896.3(DEPDC5):c.1664G>A (p.Arg555Gln)
NM_001242896.3(DEPDC5):c.1700G>A (p.Arg567Gln)
NM_001242896.3(DEPDC5):c.1704C>G (p.Asp568Glu)
NM_001242896.3(DEPDC5):c.1775C>T (p.Thr592Met)
NM_001242896.3(DEPDC5):c.1871-4G>T
NM_001242896.3(DEPDC5):c.1877C>A (p.Ser626Tyr)
NM_001242896.3(DEPDC5):c.194-3T>C
NM_001242896.3(DEPDC5):c.2035G>A (p.Gly679Ser)
NM_001242896.3(DEPDC5):c.2098G>T (p.Gly700Cys)
NM_001242896.3(DEPDC5):c.2101G>A (p.Ala701Thr)
NM_001242896.3(DEPDC5):c.2161C>A (p.Pro721Thr)
NM_001242896.3(DEPDC5):c.224A>C (p.Gln75Pro)
NM_001242896.3(DEPDC5):c.2281C>T (p.Pro761Ser)
NM_001242896.3(DEPDC5):c.2288G>T (p.Arg763Leu)
NM_001242896.3(DEPDC5):c.2335C>G (p.Pro779Ala)
NM_001242896.3(DEPDC5):c.2387A>G (p.Gln796Arg)
NM_001242896.3(DEPDC5):c.257A>G (p.Tyr86Cys)
NM_001242896.3(DEPDC5):c.2590A>G (p.Thr864Ala)
NM_001242896.3(DEPDC5):c.2715G>C (p.Trp905Cys)
NM_001242896.3(DEPDC5):c.2745G>T (p.Glu915Asp)
NM_001242896.3(DEPDC5):c.2808T>G (p.Ile936Met)
NM_001242896.3(DEPDC5):c.2921G>A (p.Arg974His)
NM_001242896.3(DEPDC5):c.2935G>A (p.Glu979Lys)
NM_001242896.3(DEPDC5):c.2942A>G (p.Gln981Arg)
NM_001242896.3(DEPDC5):c.3017T>C (p.Met1006Thr)
NM_001242896.3(DEPDC5):c.3019C>T (p.Arg1007Trp)
NM_001242896.3(DEPDC5):c.3049A>G (p.Met1017Val)
NM_001242896.3(DEPDC5):c.3068C>T (p.Thr1023Met)
NM_001242896.3(DEPDC5):c.3071A>C (p.His1024Pro)
NM_001242896.3(DEPDC5):c.3170A>C (p.Gln1057Pro)
NM_001242896.3(DEPDC5):c.3202G>C (p.Ala1068Pro)
NM_001242896.3(DEPDC5):c.3203C>T (p.Ala1068Val)
NM_001242896.3(DEPDC5):c.3223A>G (p.Ser1075Gly)
NM_001242896.3(DEPDC5):c.3224G>A (p.Ser1075Asn)
NM_001242896.3(DEPDC5):c.3242C>T (p.Thr1081Ile)
NM_001242896.3(DEPDC5):c.3269G>A (p.Gly1090Glu)
NM_001242896.3(DEPDC5):c.3302G>A (p.Arg1101His)
NM_001242896.3(DEPDC5):c.3340G>C (p.Asp1114His)
NM_001242896.3(DEPDC5):c.3380G>T (p.Gly1127Val)
NM_001242896.3(DEPDC5):c.3416G>C (p.Ser1139Thr)
NM_001242896.3(DEPDC5):c.3425T>C (p.Phe1142Ser)
NM_001242896.3(DEPDC5):c.3479A>T (p.Asp1160Val)
NM_001242896.3(DEPDC5):c.3564-3C>G
NM_001242896.3(DEPDC5):c.3578T>A (p.Leu1193Gln)
NM_001242896.3(DEPDC5):c.3605C>T (p.Pro1202Leu)
NM_001242896.3(DEPDC5):c.3623C>T (p.Ala1208Val)
NM_001242896.3(DEPDC5):c.3652G>A (p.Val1218Met)
NM_001242896.3(DEPDC5):c.3695A>G (p.Gln1232Arg)
NM_001242896.3(DEPDC5):c.3731C>G (p.Ser1244Cys)
NM_001242896.3(DEPDC5):c.3732T>A (p.Ser1244=)
NM_001242896.3(DEPDC5):c.373T>C (p.Cys125Arg)
NM_001242896.3(DEPDC5):c.3746G>A (p.Arg1249Gln)
NM_001242896.3(DEPDC5):c.3785C>T (p.Thr1262Met)
NM_001242896.3(DEPDC5):c.3823G>A (p.Ala1275Thr)
NM_001242896.3(DEPDC5):c.3827C>T (p.Thr1276Ile)
NM_001242896.3(DEPDC5):c.3853G>A (p.Asp1285Asn)
NM_001242896.3(DEPDC5):c.3940C>T (p.Pro1314Ser)
NM_001242896.3(DEPDC5):c.3946C>G (p.Leu1316Val)
NM_001242896.3(DEPDC5):c.3989T>A (p.Phe1330Tyr)
NM_001242896.3(DEPDC5):c.3999T>G (p.Ser1333Arg)
NM_001242896.3(DEPDC5):c.4014C>G (p.Ser1338Arg)
NM_001242896.3(DEPDC5):c.4096C>T (p.Arg1366Trp)
NM_001242896.3(DEPDC5):c.414A>G (p.Arg138=)
NM_001242896.3(DEPDC5):c.4264G>A (p.Gly1422Arg)
NM_001242896.3(DEPDC5):c.4296C>T (p.Gly1432=)
NM_001242896.3(DEPDC5):c.4299C>A (p.Asp1433Glu)
NM_001242896.3(DEPDC5):c.4300C>T (p.Pro1434Ser)
NM_001242896.3(DEPDC5):c.4359C>T (p.Ser1453=)
NM_001242896.3(DEPDC5):c.4376-7_4376-3del
NM_001242896.3(DEPDC5):c.4405A>G (p.Met1469Val)
NM_001242896.3(DEPDC5):c.4407G>A (p.Met1469Ile)
NM_001242896.3(DEPDC5):c.4427T>C (p.Ile1476Thr)
NM_001242896.3(DEPDC5):c.445G>A (p.Glu149Lys)
NM_001242896.3(DEPDC5):c.4484C>G (p.Pro1495Arg)
NM_001242896.3(DEPDC5):c.4559T>A (p.Phe1520Tyr)
NM_001242896.3(DEPDC5):c.4568A>C (p.Gln1523Pro)
NM_001242896.3(DEPDC5):c.4573C>T (p.Arg1525Trp)
NM_001242896.3(DEPDC5):c.4579C>T (p.Arg1527Trp)
NM_001242896.3(DEPDC5):c.4583G>A (p.Arg1528Gln)
NM_001242896.3(DEPDC5):c.4635C>G (p.Gly1545=)
NM_001242896.3(DEPDC5):c.4650C>G (p.Tyr1550Ter)
NM_001242896.3(DEPDC5):c.4738T>C (p.Cys1580Arg)
NM_001242896.3(DEPDC5):c.4745A>G (p.Asn1582Ser)
NM_001242896.3(DEPDC5):c.4748_4788delinsC (p.Arg1583fs)
NM_001242896.3(DEPDC5):c.4756C>A (p.Arg1586=)
NM_001242896.3(DEPDC5):c.4795C>T (p.His1599Tyr)
NM_001242896.3(DEPDC5):c.4808C>T (p.Pro1603Leu)
NM_001242896.3(DEPDC5):c.500C>T (p.Thr167Met)
NM_001242896.3(DEPDC5):c.504G>A (p.Ser168=)
NM_001242896.3(DEPDC5):c.532A>G (p.Ser178Gly)
NM_001242896.3(DEPDC5):c.563-3C>G
NM_001242896.3(DEPDC5):c.572A>G (p.Tyr191Cys)
NM_001242896.3(DEPDC5):c.590_592del (p.Asn197_Gly198delinsSer)
NM_001242896.3(DEPDC5):c.718G>A (p.Ala240Thr)
NM_001242896.3(DEPDC5):c.82A>G (p.Lys28Glu)
NM_001242896.3(DEPDC5):c.920T>G (p.Leu307Arg)
NM_001242896.3(DEPDC5):c.974A>G (p.Asn325Ser)
NM_001242896.3(DEPDC5):c.994A>G (p.Met332Val)
NM_001242897.2(DEPDC5):c.1010C>G (p.Thr337Arg) rs1037878155
NM_001242897.2(DEPDC5):c.1153C>T (p.Arg385Trp) rs200020310
NM_001242897.2(DEPDC5):c.1154G>A (p.Arg385Gln) rs368032858
NM_001242897.2(DEPDC5):c.1174C>T (p.Arg392Cys) rs1028964149
NM_001242897.2(DEPDC5):c.1226C>G (p.Thr409Arg) rs773704927
NM_001242897.2(DEPDC5):c.1234_1235delinsTA (p.Ser412Tyr) rs1602010588
NM_001242897.2(DEPDC5):c.1249A>T (p.Asn417Tyr) rs763518514
NM_001242897.2(DEPDC5):c.1291G>A (p.Ala431Thr) rs777844378
NM_001242897.2(DEPDC5):c.1354G>A (p.Ala452Thr) rs768264302
NM_001242897.2(DEPDC5):c.1381G>A (p.Ala461Thr) rs771161131
NM_001242897.2(DEPDC5):c.1411G>A (p.Gly471Ser) rs756780050
NM_001242897.2(DEPDC5):c.1446-8C>A rs188460159
NM_001242897.2(DEPDC5):c.1466G>A (p.Ser489Asn) rs200209747
NM_001242897.2(DEPDC5):c.1594A>G (p.Ile532Val) rs764496748
NM_001242897.2(DEPDC5):c.167A>G (p.Lys56Arg) rs966689579
NM_001242897.2(DEPDC5):c.1720A>G (p.Arg574Gly) rs762484005
NM_001242897.2(DEPDC5):c.1729G>A (p.Val577Ile) rs573430885
NM_001242897.2(DEPDC5):c.1870+2316G>A rs751767527
NM_001242897.2(DEPDC5):c.1870+2351A>G rs775910110
NM_001242897.2(DEPDC5):c.1870+2415G>A rs752184633
NM_001242897.2(DEPDC5):c.1870+3471C>A rs752274547
NM_001242897.2(DEPDC5):c.1870+3487C>G rs199603004
NM_001242897.2(DEPDC5):c.1870+3506T>A rs373078069
NM_001242897.2(DEPDC5):c.1870+3527A>C rs370940232
NM_001242897.2(DEPDC5):c.194-5T>C rs752848631
NM_001242897.2(DEPDC5):c.1943C>T (p.Thr648Ile) rs1569059850
NM_001242897.2(DEPDC5):c.2053C>T (p.Arg685Cys) rs745342391
NM_001242897.2(DEPDC5):c.2054G>A (p.Arg685His) rs542384516
NM_001242897.2(DEPDC5):c.2107G>C (p.Ala703Pro) rs761280493
NM_001242897.2(DEPDC5):c.2116G>A (p.Asp706Asn) rs776885208
NM_001242897.2(DEPDC5):c.2143A>G (p.Met715Val) rs370318709
NM_001242897.2(DEPDC5):c.2231C>G (p.Pro744Arg) rs746372266
NM_001242897.2(DEPDC5):c.2252C>T (p.Pro751Leu) rs370487077
NM_001242897.2(DEPDC5):c.2319G>C (p.Gln773His) rs368375649
NM_001242897.2(DEPDC5):c.233G>C (p.Arg78Pro) rs373578854
NM_001242897.2(DEPDC5):c.2342C>T (p.Thr781Met) rs200744555
NM_001242897.2(DEPDC5):c.2357C>T (p.Thr786Met) rs564667614
NM_001242897.2(DEPDC5):c.2387G>A (p.Arg796Gln) rs1602350746
NM_001242897.2(DEPDC5):c.2438G>C (p.Ser813Thr) rs185576553
NM_001242897.2(DEPDC5):c.2470G>A (p.Val824Ile) rs374944205
NM_001242897.2(DEPDC5):c.2497G>A (p.Glu833Lys) rs1214608865
NM_001242897.2(DEPDC5):c.2501G>A (p.Arg834Gln) rs781159677
NM_001242897.2(DEPDC5):c.268G>A (p.Val90Ile) rs768456731
NM_001242897.2(DEPDC5):c.2739G>A (p.Glu913=) rs370906184
NM_001242897.2(DEPDC5):c.2761C>T (p.Arg921Trp) rs375050296
NM_001242897.2(DEPDC5):c.2779A>G (p.Met927Val) rs367860294
NM_001242897.2(DEPDC5):c.2780T>A (p.Met927Lys) rs778753730
NM_001242897.2(DEPDC5):c.2787G>T (p.Arg929=) rs201690337
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.2935C>G (p.Gln979Glu) rs1602471069
NM_001242897.2(DEPDC5):c.2972A>C (p.Gln991Pro) rs761678944
NM_001242897.2(DEPDC5):c.2982G>C (p.Glu994Asp) rs753608617
NM_001242897.2(DEPDC5):c.2983A>C (p.Ser995Arg) rs754608531
NM_001242897.2(DEPDC5):c.3013A>C (p.Met1005Leu) rs768817912
NM_001242897.2(DEPDC5):c.3030+3822C>T rs772812141
NM_001242897.2(DEPDC5):c.3030+3843G>A rs1185705971
NM_001242897.2(DEPDC5):c.3030+3861C>T rs79027628
NM_001242897.2(DEPDC5):c.3161C>T (p.Ser1054Phe) rs578244490
NM_001242897.2(DEPDC5):c.3215C>A (p.Thr1072Asn) rs865860087
NM_001242897.2(DEPDC5):c.3263C>T (p.Ser1088Leu) rs376487148
NM_001242897.2(DEPDC5):c.3536A>G (p.His1179Arg) rs201765981
NM_001242897.2(DEPDC5):c.3559G>T (p.Ala1187Ser) rs867268278
NM_001242897.2(DEPDC5):c.3571C>T (p.Arg1191Cys) rs202227830
NM_001242897.2(DEPDC5):c.3576G>C (p.Lys1192Asn) rs1602677998
NM_001242897.2(DEPDC5):c.3808T>A (p.Cys1270Ser) rs771269120
NM_001242897.2(DEPDC5):c.3836C>A (p.Ser1279Tyr) rs765244692
NM_001242897.2(DEPDC5):c.3856A>C (p.Ile1286Leu) rs1555930038
NM_001242897.2(DEPDC5):c.3883G>A (p.Ala1295Thr) rs764462476
NM_001242897.2(DEPDC5):c.4006C>T (p.Arg1336Cys) rs778323702
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.4271A>G (p.Gln1424Arg) rs377585542
NM_001242897.2(DEPDC5):c.4280G>A (p.Arg1427Gln) rs200552561
NM_001242897.2(DEPDC5):c.4294A>G (p.Ser1432Gly) rs752046892
NM_001242897.2(DEPDC5):c.4433A>G (p.Asp1478Gly) rs201347461
NM_001242897.2(DEPDC5):c.4439G>A (p.Cys1480Tyr) rs776213050
NM_001242897.2(DEPDC5):c.4456C>T (p.Arg1486Trp) rs768925194
NM_001242897.2(DEPDC5):c.4478G>T (p.Ser1493Ile) rs1603019516
NM_001242897.2(DEPDC5):c.5G>A (p.Arg2Lys) rs756142773
NM_001242897.2(DEPDC5):c.694+3_694+6del rs1351154360
NM_001242897.2(DEPDC5):c.791G>A (p.Arg264Lys) rs750467533
NM_001242897.2(DEPDC5):c.842A>T (p.Tyr281Phe) rs200797928
NM_001242897.2(DEPDC5):c.90C>G (p.Phe30Leu) rs374794334
NM_001242897.2(DEPDC5):c.944A>G (p.Asn315Ser) rs555944888
NM_001242897.2(DEPDC5):c.953A>G (p.Asp318Gly) rs1064795102
NM_001242897.2(DEPDC5):c.968A>G (p.Asn323Ser) rs201776005

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.