ClinVar Miner

List of variants in gene DEPDC5 reported as likely benign for Seizures

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Total variants: 24
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HGVS dbSNP
NM_001242897.2(DEPDC5):c.1080T>C (p.Asn360=) rs1400775260
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.1389C>T (p.Asp463=) rs188147862
NM_001242897.2(DEPDC5):c.1416A>G (p.Pro472=) rs930376201
NM_001242897.2(DEPDC5):c.1870+3480C>G rs372975881
NM_001242897.2(DEPDC5):c.1870+3495C>T rs779428450
NM_001242897.2(DEPDC5):c.2053C>T (p.Arg685Cys)
NM_001242897.2(DEPDC5):c.2438G>C (p.Ser813Thr) rs185576553
NM_001242897.2(DEPDC5):c.2457A>C (p.Ser819=)
NM_001242897.2(DEPDC5):c.252T>C (p.Asp84=) rs183443533
NM_001242897.2(DEPDC5):c.2550C>T (p.Ala850=)
NM_001242897.2(DEPDC5):c.2820T>C (p.Thr940=) rs372062387
NM_001242897.2(DEPDC5):c.2851A>G (p.Thr951Ala)
NM_001242897.2(DEPDC5):c.2967C>T (p.Ser989=)
NM_001242897.2(DEPDC5):c.3030+3812C>T rs371377906
NM_001242897.2(DEPDC5):c.3030+3862G>A
NM_001242897.2(DEPDC5):c.3066C>T (p.Asp1022=) rs375702574
NM_001242897.2(DEPDC5):c.3267A>G (p.Thr1089=) rs142197878
NM_001242897.2(DEPDC5):c.3343G>A (p.Val1115Met) rs201603222
NM_001242897.2(DEPDC5):c.3510C>T (p.Ala1170=) rs200033252
NM_001242897.2(DEPDC5):c.4383C>T (p.Ser1461=) rs370189053
NM_001242897.2(DEPDC5):c.4459C>T (p.Leu1487=) rs1569256444
NM_001242897.2(DEPDC5):c.4500C>T (p.Ala1500=)

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