ClinVar Miner

List of variants in gene DEPDC5 reported as likely benign for Familial focal epilepsy with variable foci

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Total variants: 69
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HGVS dbSNP
NM_001242896.3(DEPDC5):c.1278A>G (p.Ala426=) rs376799291
NM_001242896.3(DEPDC5):c.1329C>T (p.Leu443=) rs758352057
NM_001242896.3(DEPDC5):c.1449T>C (p.Ser483=) rs1461464062
NM_001242896.3(DEPDC5):c.180A>G (p.Glu60=) rs550525739
NM_001242896.3(DEPDC5):c.2271C>T (p.Thr757=) rs373009424
NM_001242896.3(DEPDC5):c.2412C>T (p.Cys804=) rs201290710
NM_001242896.3(DEPDC5):c.258T>C (p.Tyr86=) rs201609075
NM_001242896.3(DEPDC5):c.2730C>T (p.His910=) rs140039884
NM_001242896.3(DEPDC5):c.2904C>T (p.Ile968=) rs200175960
NM_001242896.3(DEPDC5):c.2934C>T (p.Asp978=) rs559006082
NM_001242896.3(DEPDC5):c.2997G>T (p.Arg999=) rs372078779
NM_001242896.3(DEPDC5):c.3069G>A (p.Thr1023=) rs201368629
NM_001242896.3(DEPDC5):c.3606G>A (p.Pro1202=) rs749703301
NM_001242896.3(DEPDC5):c.45C>T (p.Gly15=) rs373199155
NM_001242896.3(DEPDC5):c.4632C>T (p.Val1544=) rs374597058
NM_001242896.3(DEPDC5):c.4689A>G (p.Thr1563=) rs368010039
NM_001242896.3(DEPDC5):c.748T>G (p.Phe250Val) rs201429774
NM_001242897.2(DEPDC5):c.1014C>T (p.Pro338=) rs774034064
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.146+5G>A rs748264035
NM_001242897.2(DEPDC5):c.1509C>T (p.Ser503=) rs376217381
NM_001242897.2(DEPDC5):c.1525C>T (p.Arg509Cys) rs202083639
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+3480C>G rs372975881
NM_001242897.2(DEPDC5):c.1870+3495C>T rs779428450
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.2273A>G (p.Tyr758Cys) rs773004067
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.2550C>T (p.Ala850=) rs201146392
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.2772G>A (p.Ser924=) rs373751704
NM_001242897.2(DEPDC5):c.2862A>G (p.Pro954=) rs756207564
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.2967C>T (p.Ser989=) rs775749832
NM_001242897.2(DEPDC5):c.2991C>T (p.Ser997=) rs757534228
NM_001242897.2(DEPDC5):c.3007A>C (p.Thr1003Pro) rs142540948
NM_001242897.2(DEPDC5):c.3030+3812C>T rs371377906
NM_001242897.2(DEPDC5):c.3030+3862G>A rs759169213
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.3396+10C>A rs755463750
NM_001242897.2(DEPDC5):c.3505+10G>A rs201608608
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.363+6_363+7del rs748242785
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.4242C>T (p.Pro1414=) rs368918488
NM_001242897.2(DEPDC5):c.4383C>T (p.Ser1461=) rs370189053
NM_001242897.2(DEPDC5):c.4500C>T (p.Ala1500=) rs754017226
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.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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