ClinVar Miner

List of variants in gene SPAST reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 57
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HGVS dbSNP
NM_014946.3(SPAST):c.*11T>C rs753913367
NM_014946.3(SPAST):c.*1231_*1233delCAT rs376420990
NM_014946.3(SPAST):c.*1376A>G rs575900032
NM_014946.3(SPAST):c.*1410T>G rs75645928
NM_014946.3(SPAST):c.*1454G>C rs147052682
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.*19C>T rs558483397
NM_014946.3(SPAST):c.*2150G>C rs147721392
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.*244_*247delTTAG rs201733642
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.*606_*608delTGT rs142605868
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.-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.1098+19C>G
NM_014946.3(SPAST):c.1173+17A>C rs200640366
NM_014946.3(SPAST):c.1173+283dup
NM_014946.3(SPAST):c.1174-208G>A
NM_014946.3(SPAST):c.131C>T (p.Ser44Leu) rs121908515
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.416-240A>G
NM_014946.3(SPAST):c.484G>A (p.Val162Ile) rs141944844
NM_014946.3(SPAST):c.586+9_586+12delTAAT rs554544808
NM_014946.3(SPAST):c.683-9C>T rs202209866
NM_014946.3(SPAST):c.68G>A (p.Arg23Lys)
NM_014946.3(SPAST):c.816A>G (p.Leu272=) rs1239753392
NM_014946.3(SPAST):c.828T>C (p.Ser276=) rs77525846
NM_014946.3(SPAST):c.865C>T (p.His289Tyr) rs74688377
NM_014946.3(SPAST):c.870+60A>C
NM_014946.3(SPAST):c.871-12G>A rs764275621
NM_014946.3(SPAST):c.879G>A (p.Pro293=) rs145264166
NM_014946.3(SPAST):c.942G>A (p.Leu314=) rs776121105

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