ClinVar Miner

List of variants in gene DEPDC5 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 68
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HGVS dbSNP
NM_001242897.2(DEPDC5):c.1014C>T (p.Pro338=) rs774034064
NM_001242897.2(DEPDC5):c.1230C>G (p.Ser410=) rs771613005
NM_001242897.2(DEPDC5):c.1245T>C (p.Phe415=) rs1555880783
NM_001242897.2(DEPDC5):c.1290C>T (p.Pro430=) rs201202102
NM_001242897.2(DEPDC5):c.1321A>G (p.Thr441Ala) rs199749859
NM_001242897.2(DEPDC5):c.1330G>A (p.Gly444Arg) rs201394709
NM_001242897.2(DEPDC5):c.1380C>T (p.Asp460=) rs375451146
NM_001242897.2(DEPDC5):c.138T>A (p.Asp46Glu) rs535630975
NM_001242897.2(DEPDC5):c.1416A>G (p.Pro472=) rs930376201
NM_001242897.2(DEPDC5):c.146+5G>A rs748264035
NM_001242897.2(DEPDC5):c.1509C>T (p.Ser503=) rs376217381
NM_001242897.2(DEPDC5):c.1758T>C (p.Val586=) rs766732676
NM_001242897.2(DEPDC5):c.1803C>T (p.Phe601=) rs368563183
NM_001242897.2(DEPDC5):c.1870+10T>C rs760092505
NM_001242897.2(DEPDC5):c.1870+3480C>G rs372975881
NM_001242897.2(DEPDC5):c.1870+3495C>T rs779428450
NM_001242897.2(DEPDC5):c.1937-10C>T rs746913609
NM_001242897.2(DEPDC5):c.1937-9G>A rs770492339
NM_001242897.2(DEPDC5):c.2019G>A (p.Ala673=) rs777616535
NM_001242897.2(DEPDC5):c.204T>C (p.Ser68=) rs774206363
NM_001242897.2(DEPDC5):c.2127C>T (p.Asp709=) rs371165640
NM_001242897.2(DEPDC5):c.2133T>C (p.Asp711=) rs751377415
NM_001242897.2(DEPDC5):c.2281+10T>C rs1276307484
NM_001242897.2(DEPDC5):c.2343G>A (p.Thr781=) rs375938114
NM_001242897.2(DEPDC5):c.2358G>A (p.Thr786=) rs763764167
NM_001242897.2(DEPDC5):c.252T>C (p.Asp84=) rs183443533
NM_001242897.2(DEPDC5):c.2628C>T (p.Thr876=) rs1027803497
NM_001242897.2(DEPDC5):c.262A>G (p.Asn88Asp) rs144712084
NM_001242897.2(DEPDC5):c.2646G>A (p.Thr882=) rs767693306
NM_001242897.2(DEPDC5):c.2772G>A (p.Ser924=) rs373751704
NM_001242897.2(DEPDC5):c.2820T>C (p.Thr940=) rs372062387
NM_001242897.2(DEPDC5):c.2823G>A (p.Gly941=) rs1060504242
NM_001242897.2(DEPDC5):c.2862A>G (p.Pro954=) rs756207564
NM_001242897.2(DEPDC5):c.2889C>T (p.Leu963=) rs1555901654
NM_001242897.2(DEPDC5):c.2921A>G (p.Lys974Arg) rs200277794
NM_001242897.2(DEPDC5):c.2943A>G (p.Ala981=) rs776608344
NM_001242897.2(DEPDC5):c.2979C>G (p.Ala993=) rs373166302
NM_001242897.2(DEPDC5):c.2991C>T (p.Ser997=) rs757534228
NM_001242897.2(DEPDC5):c.3030+3812C>T rs371377906
NM_001242897.2(DEPDC5):c.3030+3865C>T rs371969641
NM_001242897.2(DEPDC5):c.3031-10del rs377356885
NM_001242897.2(DEPDC5):c.3066C>T (p.Asp1022=) rs375702574
NM_001242897.2(DEPDC5):c.3186-5dup rs1555914747
NM_001242897.2(DEPDC5):c.3396+10C>A rs755463750
NM_001242897.2(DEPDC5):c.3498C>T (p.Pro1166=) rs376187025
NM_001242897.2(DEPDC5):c.3505+10G>A rs201608608
NM_001242897.2(DEPDC5):c.3506-8T>C rs1555919097
NM_001242897.2(DEPDC5):c.351A>G (p.Leu117=) rs746535603
NM_001242897.2(DEPDC5):c.3537C>T (p.His1179=) rs370472498
NM_001242897.2(DEPDC5):c.3546A>G (p.Gly1182=) rs771875089
NM_001242897.2(DEPDC5):c.3558C>T (p.Phe1186=) rs192246855
NM_001242897.2(DEPDC5):c.3648G>A (p.Leu1216=) rs371864100
NM_001242897.2(DEPDC5):c.3777C>T (p.Asp1259=) rs573674033
NM_001242897.2(DEPDC5):c.4086C>T (p.Pro1362=) rs754105028
NM_001242897.2(DEPDC5):c.4092G>A (p.Thr1364=) rs756506370
NM_001242897.2(DEPDC5):c.4137G>A (p.Arg1379=) rs1057522689
NM_001242897.2(DEPDC5):c.4242C>T (p.Pro1414=) rs368918488
NM_001242897.2(DEPDC5):c.4347C>G (p.Ala1449=) rs1555943168
NM_001242897.2(DEPDC5):c.4383C>T (p.Ser1461=) rs370189053
NM_001242897.2(DEPDC5):c.4509G>A (p.Pro1503=) rs201307299
NM_001242897.2(DEPDC5):c.453C>T (p.Val151=) rs558913954
NM_001242897.2(DEPDC5):c.633C>T (p.Asn211=) rs771270766
NM_001242897.2(DEPDC5):c.711A>C (p.Ile237=) rs368571578
NM_001242897.2(DEPDC5):c.71T>G (p.Val24Gly) rs572660873
NM_001242897.2(DEPDC5):c.813C>T (p.Leu271=) rs200547310
NM_001242897.2(DEPDC5):c.871+9T>C rs373471598
NM_001242897.2(DEPDC5):c.879T>C (p.Phe293=) rs1335286901
NM_001242897.2(DEPDC5):c.946+10G>C rs367917127

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