ClinVar Miner

List of variants in gene CLN8 reported as likely pathogenic for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_018941.3(CLN8):c.181_183del (p.Lys61del) rs386834123
NM_018941.3(CLN8):c.204del (p.Thr69fs) rs1554449028
NM_018941.3(CLN8):c.209G>A (p.Arg70His) rs386834124
NM_018941.3(CLN8):c.226C>T (p.Gln76Ter) rs1554449047
NM_018941.3(CLN8):c.227A>G (p.Gln76Arg) rs386834125
NM_018941.3(CLN8):c.263del (p.Asp88fs) rs1057516582
NM_018941.3(CLN8):c.283A>T (p.Lys95Ter) rs759830733
NM_018941.3(CLN8):c.2T>C (p.Met1Thr) rs1554448874
NM_018941.3(CLN8):c.306G>A (p.Trp102Ter) rs1554449124
NM_018941.3(CLN8):c.312G>A (p.Trp104Ter) rs1554449136
NM_018941.3(CLN8):c.320T>G (p.Ile107Ser) rs386834126
NM_018941.3(CLN8):c.398T>A (p.Leu133Ter) rs554042394
NM_018941.3(CLN8):c.415C>T (p.His139Tyr) rs386834127
NM_018941.3(CLN8):c.464C>T (p.Ala155Val) rs386834128
NM_018941.3(CLN8):c.46C>A (p.Leu16Met) rs386834129
NM_018941.3(CLN8):c.470A>G (p.His157Arg) rs149308952
NM_018941.3(CLN8):c.473A>G (p.Tyr158Cys) rs386834130
NM_018941.3(CLN8):c.47del (p.Leu16fs) rs1057516867
NM_018941.3(CLN8):c.499G>T (p.Glu167Ter) rs144495588
NM_018941.3(CLN8):c.507C>T (p.Ser169=) rs386834131
NM_018941.3(CLN8):c.509C>T (p.Thr170Met) rs188259026
NM_018941.3(CLN8):c.50del (p.Asp17fs) rs1554448924
NM_018941.3(CLN8):c.543+1G>T rs756267448
NM_018941.3(CLN8):c.544-2A>G rs1554451484
NM_018941.3(CLN8):c.562_563delCT rs386834132
NM_018941.3(CLN8):c.581A>G (p.Gln194Arg) rs386834133
NM_018941.3(CLN8):c.594del (p.His199fs) rs1554451504
NM_018941.3(CLN8):c.610C>T (p.Arg204Cys) rs104894060
NM_018941.3(CLN8):c.611G>T (p.Arg204Leu) rs386834134
NM_018941.3(CLN8):c.634_636TGG[1] (p.Trp213del) rs386834135
NM_018941.3(CLN8):c.661G>A (p.Gly221Ser) rs386834136
NM_018941.3(CLN8):c.66del (p.Ile23fs) rs34238807
NM_018941.3(CLN8):c.709G>A (p.Gly237Arg) rs746645358
NM_018941.3(CLN8):c.763C>T (p.Gln255Ter) rs746397087
NM_018941.3(CLN8):c.766C>G (p.Gln256Glu) rs386834138
NM_018941.3(CLN8):c.88del (p.Ala30fs) rs386834139
NM_018941.3(CLN8):c.[208C>T;792C>G]
NM_018941.3(CLN8):c.[212C>T];[562_563delCT]

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