ClinVar Miner

List of variants in gene CLN6 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (88):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
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HGVS dbSNP
NM_017882.3(CLN6):c.*393G>A
NM_017882.3(CLN6):c.*646C>G rs144976448
NM_017882.3(CLN6):c.*655C>T
NM_017882.3(CLN6):c.*75G>C
NM_017882.3(CLN6):c.*934G>T rs114551417
NM_017882.3(CLN6):c.135C>T (p.Leu45=) rs374577694
NM_017882.3(CLN6):c.13C>A (p.Arg5=) rs886285802
NM_017882.3(CLN6):c.195C>T (p.Ala65=) rs1472031434
NM_017882.3(CLN6):c.199-5C>T rs371705916
NM_017882.3(CLN6):c.204A>G (p.Val68=) rs774960579
NM_017882.3(CLN6):c.213C>G (p.Leu71=) rs146980624
NM_017882.3(CLN6):c.213C>T (p.Leu71=) rs146980624
NM_017882.3(CLN6):c.240T>C (p.Ser80=) rs1395492951
NM_017882.3(CLN6):c.279G>A (p.Thr93=) rs746613593
NM_017882.3(CLN6):c.282C>A (p.Pro94=) rs139261571
NM_017882.3(CLN6):c.303C>T (p.Ile101=) rs1369226101
NM_017882.3(CLN6):c.396T>C (p.Ser132=) rs949403836
NM_017882.3(CLN6):c.42C>A (p.Gly14=) rs373776911
NM_017882.3(CLN6):c.477G>A (p.Pro159=) rs370811678
NM_017882.3(CLN6):c.489C>T (p.Ile163=) rs748682605
NM_017882.3(CLN6):c.543-9C>T rs374653673
NM_017882.3(CLN6):c.564C>A (p.Ile188=) rs371326037
NM_017882.3(CLN6):c.567C>T (p.Leu189=) rs762214934
NM_017882.3(CLN6):c.585C>T (p.Gly195=) rs144507672
NM_017882.3(CLN6):c.5A>G (p.Glu2Gly) rs3743088
NM_017882.3(CLN6):c.64G>T (p.Ala22Ser) rs527373013
NM_017882.3(CLN6):c.678C>T (p.Thr226=) rs374744816
NM_017882.3(CLN6):c.717C>T (p.Phe239=) rs745850620
NM_017882.3(CLN6):c.741C>T (p.His247=) rs140653271
NM_017882.3(CLN6):c.755G>A (p.Arg252His) rs374681194
NM_017882.3(CLN6):c.769A>G (p.Ser257Gly) rs151295143
NM_017882.3(CLN6):c.798C>T (p.Phe266=) rs140319056
NM_017882.3(CLN6):c.801A>G (p.Ala267=) rs901756486
NM_017882.3(CLN6):c.822G>A (p.Ala274=) rs151186473
NM_017882.3(CLN6):c.831C>T (p.Val277=) rs753344266
NM_017882.3(CLN6):c.84-8C>T rs756782429
NM_017882.3(CLN6):c.858C>T (p.Leu286=) rs1043430340
NM_017882.3(CLN6):c.885C>T (p.Tyr295=) rs374990526
NM_017882.3(CLN6):c.912C>T (p.Thr304=) rs201330867
NM_017882.3(CLN6):c.924C>T (p.Ser308=) rs774237925
NM_017882.3(CLN6):c.93T>C (p.Ser31=) rs376510900
NM_017882.3(CLN6):c.99C>T (p.Ser33=) rs752449801

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