ClinVar Miner

List of variants in gene SLC33A1 reported as likely benign for Spastic paraplegia, autosomal dominant

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Total variants: 14
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HGVS dbSNP
NM_004733.4(SLC33A1):c.*105G>A rs528825751
NM_004733.4(SLC33A1):c.*1141A>T rs77664705
NM_004733.4(SLC33A1):c.*1673_*1676del rs143606890
NM_004733.4(SLC33A1):c.*169del rs139894444
NM_004733.4(SLC33A1):c.*322A>G rs144921458
NM_004733.4(SLC33A1):c.*510A>T rs550090276
NM_004733.4(SLC33A1):c.-125C>T rs144110429
NM_004733.4(SLC33A1):c.-33C>G rs192078418
NM_004733.4(SLC33A1):c.-43C>T rs140074495
NM_004733.4(SLC33A1):c.136G>A (p.Glu46Lys) rs149571533
NM_004733.4(SLC33A1):c.1451A>C (p.Asn484Thr) rs144015992
NM_004733.4(SLC33A1):c.1525G>A (p.Gly509Ser) rs76440173
NM_004733.4(SLC33A1):c.169G>C (p.Gly57Arg) rs150651158
NM_004733.4(SLC33A1):c.327A>G (p.Gln109=) rs74578336

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