ClinVar Miner

List of variants in gene ST3GAL5 reported as likely benign for Amish infantile epilepsy syndrome

Included ClinVar conditions (1):
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Gene type:
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Total variants: 10
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HGVS dbSNP
NM_003896.4(ST3GAL5):c.1036G>A (p.Val346Ile) rs145738225
NM_003896.4(ST3GAL5):c.1170T>C (p.Asn390=) rs1229066524
NM_003896.4(ST3GAL5):c.1212G>A (p.Glu404=) rs148195895
NM_003896.4(ST3GAL5):c.155G>A (p.Arg52Gln) rs141917910
NM_003896.4(ST3GAL5):c.37C>T (p.Pro13Ser) rs559756386
NM_003896.4(ST3GAL5):c.414C>T (p.Ser138=) rs368878731
NM_003896.4(ST3GAL5):c.474C>T (p.Tyr158=) rs150855708
NM_003896.4(ST3GAL5):c.522C>G (p.Leu174=) rs766829186
NM_003896.4(ST3GAL5):c.546C>T (p.Asp182=) rs147315816
NM_003896.4(ST3GAL5):c.778T>C (p.Leu260=) rs752738939

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