ClinVar Miner

List of variants in gene TUBA1A reported as uncertain significance

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Total variants: 33
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HGVS dbSNP
NM_001270399.1(TUBA1A):c.-663C>T rs886049496
NM_001270399.1(TUBA1A):c.-766A>G rs886049497
NM_006009.4(TUBA1A):c.*1del (p.Ter452=) rs781483247
NM_006009.4(TUBA1A):c.-64G>A rs886049494
NM_006009.4(TUBA1A):c.-69G>T rs371310839
NM_006009.4(TUBA1A):c.-78C>T rs574389302
NM_006009.4(TUBA1A):c.-99A>T rs886049495
NM_006009.4(TUBA1A):c.1082C>T (p.Thr361Ile) rs1555162301
NM_006009.4(TUBA1A):c.1224C>A (p.Tyr408Ter) rs753719501
NM_006009.4(TUBA1A):c.1232A>G (p.Glu411Gly) rs1565626917
NM_006009.4(TUBA1A):c.1247G>A (p.Gly416Asp) rs1565626906
NM_006009.4(TUBA1A):c.1248T>C (p.Gly416=) rs3206694
NM_006009.4(TUBA1A):c.1291G>A (p.Asp431Asn) rs1361084932
NM_006009.4(TUBA1A):c.1298_1300AGG[1] (p.Glu434del) rs1555162244
NM_006009.4(TUBA1A):c.235C>T (p.Arg79Cys) rs1555162507
NM_006009.4(TUBA1A):c.273A>G (p.Gln91=) rs765483435
NM_006009.4(TUBA1A):c.276T>C (p.Leu92=) rs1065671
NM_006009.4(TUBA1A):c.344T>C (p.Ile115Thr) rs1085307716
NM_006009.4(TUBA1A):c.376-10T>A rs886049493
NM_006009.4(TUBA1A):c.379G>A (p.Asp127Asn) rs1085308005
NM_006009.4(TUBA1A):c.390G>C (p.Thr130=) rs1143559
NM_006009.4(TUBA1A):c.4-10C>T rs757244916
NM_006009.4(TUBA1A):c.4-7C>T rs560491477
NM_006009.4(TUBA1A):c.521C>T (p.Ala174Val) rs587784489
NM_006009.4(TUBA1A):c.53A>G (p.Asn18Ser) rs1064795213
NM_006009.4(TUBA1A):c.562_564dup (p.Ile188dup) rs587784490
NM_006009.4(TUBA1A):c.640C>A (p.Arg214Ser) rs886044568
NM_006009.4(TUBA1A):c.663T>C (p.Arg221=) rs754280693
NM_006009.4(TUBA1A):c.733G>A (p.Asp245Asn) rs1555162357
NM_006009.4(TUBA1A):c.758C>G (p.Thr253Arg) rs587784493
NM_006009.4(TUBA1A):c.791G>A (p.Arg264His) rs886043627
NM_006009.4(TUBA1A):c.96C>T (p.Pro32=) rs139102191
NM_006009.4(TUBA1A):c.991G>A (p.Ala331Thr) rs587784496

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