ClinVar Miner

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

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 8
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NM_003896.3(ST3GAL5):c.-140C>A rs28364795
NM_003896.3(ST3GAL5):c.-141T>C rs28364794
NM_003896.4(ST3GAL5):c.311A>G (p.His104Arg) rs1138484
NM_003896.4(ST3GAL5):c.37C>T (p.Pro13Ser) rs559756386
NM_003896.4(ST3GAL5):c.390G>A (p.Ala130=) rs144270260
NM_003896.4(ST3GAL5):c.465G>A (p.Glu155=) rs199590656
NM_003896.4(ST3GAL5):c.648C>T (p.Phe216=) rs149309844
NM_003896.4(ST3GAL5):c.850-5C>T rs113976691

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