ClinVar Miner

List of variants in gene SPAST reported as likely benign for not specified

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 20
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HGVS dbSNP
NM_014946.3(SPAST):c.*11T>C rs753913367
NM_014946.3(SPAST):c.-41C>T rs374327295
NM_014946.3(SPAST):c.1077T>C (p.Ile359=) rs570106557
NM_014946.3(SPAST):c.1087C>T (p.Leu363=) rs769858706
NM_014946.3(SPAST):c.1173+17A>C rs200640366
NM_014946.3(SPAST):c.1321+9A>G rs201349526
NM_014946.3(SPAST):c.1493+18G>T rs189961829
NM_014946.3(SPAST):c.1493+6G>A rs115659052
NM_014946.3(SPAST):c.1536+17G>T rs201026422
NM_014946.3(SPAST):c.1617-3C>T rs201212542
NM_014946.3(SPAST):c.171G>C (p.Leu57=) rs1057523187
NM_014946.3(SPAST):c.1728+16A>G rs76494041
NM_014946.3(SPAST):c.289C>A (p.Pro97Thr) rs372005558
NM_014946.3(SPAST):c.327G>C (p.Pro109=) rs1033468634
NM_014946.3(SPAST):c.415+12G>A rs539075273
NM_014946.3(SPAST):c.415+17G>T rs748969302
NM_014946.3(SPAST):c.816A>G (p.Leu272=) rs1239753392
NM_014946.3(SPAST):c.865C>T (p.His289Tyr) rs74688377
NM_014946.3(SPAST):c.871-12G>A rs764275621
NM_014946.3(SPAST):c.942G>A (p.Leu314=) rs776121105

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