ClinVar Miner

List of variants in gene SPAST reported as benign for Spastic paraplegia 4, autosomal dominant

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Gene type:
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Total variants: 34
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HGVS dbSNP
NM_014946.3(SPAST):c.*1410T>G rs75645928
NM_014946.3(SPAST):c.*1454G>C rs147052682
NM_014946.3(SPAST):c.*1544G>T rs6709048
NM_014946.3(SPAST):c.*1545T>G rs9789593
NM_014946.3(SPAST):c.*1604G>A rs192438402
NM_014946.3(SPAST):c.*1962A>G rs187724468
NM_014946.3(SPAST):c.*1963A>G rs192476121
NM_014946.3(SPAST):c.*1969A>T rs533154653
NM_014946.3(SPAST):c.*1995A>G rs540679757
NM_014946.3(SPAST):c.*2150G>C rs147721392
NM_014946.3(SPAST):c.*2264G>A rs3769602
NM_014946.3(SPAST):c.*2318G>A rs141017850
NM_014946.3(SPAST):c.*2399C>T rs72796869
NM_014946.3(SPAST):c.*2433A>G rs569779105
NM_014946.3(SPAST):c.*256A>G rs6730400
NM_014946.3(SPAST):c.*2583C>T rs138968325
NM_014946.3(SPAST):c.*2589T>G rs149425698
NM_014946.3(SPAST):c.*3013T>C rs72796870
NM_014946.3(SPAST):c.*51A>G rs6730121
NM_014946.3(SPAST):c.*591A>T rs115996749
NM_014946.3(SPAST):c.*765A>C rs141666739
NM_014946.3(SPAST):c.*819C>T rs186529600
NM_014946.3(SPAST):c.*98A>G rs56272862
NM_014946.3(SPAST):c.131C>T (p.Ser44Leu) rs121908515
NM_014946.3(SPAST):c.1493+18G>T rs189961829
NM_014946.3(SPAST):c.1493+6G>A rs115659052
NM_014946.3(SPAST):c.1494-3dup rs760322678
NM_014946.3(SPAST):c.1735A>C (p.Asn579His) rs144594804
NM_014946.3(SPAST):c.289C>A (p.Pro97Thr) rs372005558
NM_014946.3(SPAST):c.484G>A (p.Val162Ile) rs141944844
NM_014946.3(SPAST):c.683-9C>T rs202209866
NM_014946.3(SPAST):c.865C>T (p.His289Tyr) rs74688377
NM_014946.4(SPAST):c.878C>T (p.Pro293Leu)
NM_014946.4(SPAST):c.879G>A (p.Pro293=) rs145264166

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