ClinVar Miner

List of variants in gene MFSD8 reported as likely benign for adolescent-onset epilepsy syndrome

Included ClinVar conditions (80):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
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HGVS dbSNP
NM_152778.2(MFSD8):c.1320A>G (p.Leu440=) rs148864710
NM_152778.2(MFSD8):c.1470A>G (p.Gly490=) rs1477527807
NM_152778.2(MFSD8):c.155-9delT rs1060504501
NM_152778.2(MFSD8):c.206C>T (p.Pro69Leu) rs147750747
NM_152778.2(MFSD8):c.270T>A (p.Ala90=) rs754809138
NM_152778.2(MFSD8):c.435A>C (p.Gly145=) rs781299975
NM_152778.2(MFSD8):c.590G>A (p.Gly197Asp) rs28544073
NM_152778.2(MFSD8):c.63-4C>T rs764964269
NM_152778.2(MFSD8):c.63-4delC rs755011754
NM_152778.2(MFSD8):c.78A>G (p.Leu26=) rs770986122
NM_152778.2(MFSD8):c.813C>T (p.Ala271=) rs768499490
NM_152778.2(MFSD8):c.840A>G (p.Leu280=) rs199982542

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