ClinVar Miner

List of variants in gene SLC33A1 studied for Spastic paraplegia, autosomal dominant

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Total variants: 37
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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.*1200T>C rs886058102
NM_004733.4(SLC33A1):c.*1230A>G rs886058101
NM_004733.4(SLC33A1):c.*149C>T rs886058107
NM_004733.4(SLC33A1):c.*1529C>T rs886058100
NM_004733.4(SLC33A1):c.*1619A>G rs10513483
NM_004733.4(SLC33A1):c.*1673_*1676del rs143606890
NM_004733.4(SLC33A1):c.*169del rs139894444
NM_004733.4(SLC33A1):c.*179dup rs201290926
NM_004733.4(SLC33A1):c.*322A>G rs144921458
NM_004733.4(SLC33A1):c.*509G>T rs886058106
NM_004733.4(SLC33A1):c.*510A>T rs550090276
NM_004733.4(SLC33A1):c.*582_*583del rs762573505
NM_004733.4(SLC33A1):c.*595A>C rs886058105
NM_004733.4(SLC33A1):c.*746T>G rs774751936
NM_004733.4(SLC33A1):c.*755C>T rs189496085
NM_004733.4(SLC33A1):c.*869G>A rs886058104
NM_004733.4(SLC33A1):c.*893del rs886058103
NM_004733.4(SLC33A1):c.-125C>T rs144110429
NM_004733.4(SLC33A1):c.-27C>T rs777838988
NM_004733.4(SLC33A1):c.-281C>T rs560777515
NM_004733.4(SLC33A1):c.-33C>G rs192078418
NM_004733.4(SLC33A1):c.-343G>A rs1131925
NM_004733.4(SLC33A1):c.-43C>T rs140074495
NM_004733.4(SLC33A1):c.1068G>A (p.Gln356=) rs886058108
NM_004733.4(SLC33A1):c.1149-4A>G rs773106675
NM_004733.4(SLC33A1):c.1267-4G>A rs779467886
NM_004733.4(SLC33A1):c.131G>T (p.Gly44Val) rs780400607
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
NM_004733.4(SLC33A1):c.512A>G (p.Asp171Gly) rs3804769
NM_004733.4(SLC33A1):c.613T>C (p.Leu205=) rs886058110
NM_004733.4(SLC33A1):c.904T>C (p.Phe302Leu) rs886058109

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