ClinVar Miner

List of variants in gene GAL reported as uncertain significance for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_015973.3:c.82del
NM_015973.5(GAL):c.137-2A>G
NM_015973.5(GAL):c.140C>T (p.Ala47Val) rs374472664
NM_015973.5(GAL):c.166G>A (p.Asp56Asn)
NM_015973.5(GAL):c.178C>T (p.Leu60Phe)
NM_015973.5(GAL):c.199C>T (p.Arg67Trp) rs200075890
NM_015973.5(GAL):c.205G>A (p.Glu69Lys) rs571107777
NM_015973.5(GAL):c.263G>A (p.Arg88His) rs778530092
NM_015973.5(GAL):c.43G>A (p.Ala15Thr)
NM_015973.5(GAL):c.55T>C (p.Ser19Pro) rs746008445

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