ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 38
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HGVS dbSNP
NM_014946.3(SPAST):c.*1156T>C rs546193636
NM_014946.3(SPAST):c.*11T>C rs753913367
NM_014946.3(SPAST):c.*1231C>T rs886055974
NM_014946.3(SPAST):c.*1476A>G rs760307887
NM_014946.3(SPAST):c.*1543_*1544insT rs751815134
NM_014946.3(SPAST):c.*1544dupG rs542086083
NM_014946.3(SPAST):c.*157A>C rs886055963
NM_014946.3(SPAST):c.*1777G>A rs886055976
NM_014946.3(SPAST):c.*1783C>T rs886055977
NM_014946.3(SPAST):c.*1829C>T rs886055978
NM_014946.3(SPAST):c.*1858T>G rs573241334
NM_014946.3(SPAST):c.*2196A>T rs886055979
NM_014946.3(SPAST):c.*2322T>G rs530517245
NM_014946.3(SPAST):c.*2504A>G rs886055980
NM_014946.3(SPAST):c.*2658A>T rs886055981
NM_014946.3(SPAST):c.*2779G>A rs886055982
NM_014946.3(SPAST):c.*2898C>T rs886055983
NM_014946.3(SPAST):c.*2904C>T rs534543205
NM_014946.3(SPAST):c.*2987G>C rs770713063
NM_014946.3(SPAST):c.*2999dupT rs886055984
NM_014946.3(SPAST):c.*380_*383delTTGT rs756347073
NM_014946.3(SPAST):c.*382G>A rs570596299
NM_014946.3(SPAST):c.*478G>T rs886055966
NM_014946.3(SPAST):c.*494C>T rs886055967
NM_014946.3(SPAST):c.*521A>G rs886055968
NM_014946.3(SPAST):c.*533T>G rs886055969
NM_014946.3(SPAST):c.*815_*828delCTTCCTGATGGAATinsAAC rs886055971
NM_014946.3(SPAST):c.*892T>G rs886055972
NM_014946.3(SPAST):c.-104_-102delACG rs886055960
NM_014946.3(SPAST):c.-168G>A rs886055959
NM_014946.3(SPAST):c.-176C>T rs886055958
NM_014946.3(SPAST):c.-220G>T rs886055957
NM_014946.3(SPAST):c.-41C>T rs374327295
NM_014946.3(SPAST):c.-7G>A rs376165443
NM_014946.3(SPAST):c.1005-5C>A rs377123251
NM_014946.3(SPAST):c.1744T>C (p.Leu582=) rs886055962
NM_014946.3(SPAST):c.55C>T (p.Pro19Ser) rs372349942
NM_014946.3(SPAST):c.644G>A (p.Ser215Asn) rs774722817

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