ClinVar Miner

List of variants in gene SLC33A1 reported as uncertain significance for Spastic paraplegia, autosomal dominant

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Total variants: 19
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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.*509G>T rs886058106
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.-27C>T rs777838988
NM_004733.4(SLC33A1):c.-281C>T rs560777515
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.613T>C (p.Leu205=) rs886058110
NM_004733.4(SLC33A1):c.904T>C (p.Phe302Leu) rs886058109

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