ClinVar Miner

List of variants in gene TUBA1A reported as uncertain significance

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Total variants: 88
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HGVS dbSNP gnomAD frequency
NM_006009.4(TUBA1A):c.4-7C>T rs560491477 0.00053
NM_006009.4(TUBA1A):c.1248T>C (p.Gly416=) rs3206694 0.00004
NM_006009.4(TUBA1A):c.859T>A (p.Ser287Thr) rs150978489 0.00002
NM_006009.4(TUBA1A):c.1056G>C (p.Lys352Asn)
NM_006009.4(TUBA1A):c.1078C>T (p.Pro360Ser) rs2121242056
NM_006009.4(TUBA1A):c.1081A>G (p.Thr361Ala)
NM_006009.4(TUBA1A):c.1082C>T (p.Thr361Ile) rs1555162301
NM_006009.4(TUBA1A):c.1117A>G (p.Arg373Gly) rs1942165485
NM_006009.4(TUBA1A):c.1127G>A (p.Cys376Tyr) rs2121241786
NM_006009.4(TUBA1A):c.1136G>A (p.Ser379Asn)
NM_006009.4(TUBA1A):c.1154C>T (p.Ala385Val)
NM_006009.4(TUBA1A):c.1182G>C (p.Lys394Asn) rs1942164467
NM_006009.4(TUBA1A):c.1193T>G (p.Met398Arg) rs1942164218
NM_006009.4(TUBA1A):c.1204C>G (p.Arg402Gly)
NM_006009.4(TUBA1A):c.1222T>G (p.Tyr408Asp) rs2121241414
NM_006009.4(TUBA1A):c.1224C>A (p.Tyr408Ter) rs753719501
NM_006009.4(TUBA1A):c.1225G>A (p.Val409Ile) rs1565626928
NM_006009.4(TUBA1A):c.1232A>G (p.Glu411Gly)
NM_006009.4(TUBA1A):c.1237A>T (p.Met413Leu) rs2121241343
NM_006009.4(TUBA1A):c.1247G>A (p.Gly416Asp) rs1565626906
NM_006009.4(TUBA1A):c.1276G>A (p.Ala426Thr)
NM_006009.4(TUBA1A):c.1283T>A (p.Leu428His)
NM_006009.4(TUBA1A):c.1291G>A (p.Asp431Asn) rs1361084932
NM_006009.4(TUBA1A):c.1298AGG[1] (p.Glu434del) rs1555162244
NM_006009.4(TUBA1A):c.188C>T (p.Pro63Leu) rs2121247772
NM_006009.4(TUBA1A):c.226+6T>C
NM_006009.4(TUBA1A):c.227A>T (p.Asp76Val)
NM_006009.4(TUBA1A):c.235C>T (p.Arg79Cys) rs1555162507
NM_006009.4(TUBA1A):c.250C>A (p.Arg84Ser)
NM_006009.4(TUBA1A):c.251G>A (p.Arg84His) rs1400284461
NM_006009.4(TUBA1A):c.26T>C (p.Val9Ala) rs1565627795
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.326C>G (p.Thr109Ser) rs2121246504
NM_006009.4(TUBA1A):c.343A>T (p.Ile115Phe)
NM_006009.4(TUBA1A):c.34G>C (p.Ala12Pro)
NM_006009.4(TUBA1A):c.358G>T (p.Asp120Tyr) rs2121246309
NM_006009.4(TUBA1A):c.362G>A (p.Arg121Gln) rs2121246284
NM_006009.4(TUBA1A):c.367C>T (p.Arg123Cys) rs886039513
NM_006009.4(TUBA1A):c.376-1G>C rs1942175909
NM_006009.4(TUBA1A):c.377C>T (p.Ala126Val) rs2121245288
NM_006009.4(TUBA1A):c.382C>G (p.Gln128Glu)
NM_006009.4(TUBA1A):c.385T>C (p.Cys129Arg) rs1942175585
NM_006009.4(TUBA1A):c.420C>A (p.Ser140Arg)
NM_006009.4(TUBA1A):c.427G>A (p.Gly143Arg) rs1131691318
NM_006009.4(TUBA1A):c.427G>C (p.Gly143Arg)
NM_006009.4(TUBA1A):c.427G>T (p.Gly143Trp) rs1131691318
NM_006009.4(TUBA1A):c.442G>A (p.Gly148Arg) rs2121244979
NM_006009.4(TUBA1A):c.449C>T (p.Thr150Ile) rs1565627339
NM_006009.4(TUBA1A):c.455T>A (p.Leu152Gln) rs1057521063
NM_006009.4(TUBA1A):c.485G>A (p.Gly162Asp)
NM_006009.4(TUBA1A):c.489del (p.Lys164fs)
NM_006009.4(TUBA1A):c.48del (p.Ile16fs)
NM_006009.4(TUBA1A):c.518C>T (p.Pro173Leu) rs1565627304
NM_006009.4(TUBA1A):c.521C>T (p.Ala174Val) rs587784489
NM_006009.4(TUBA1A):c.527A>T (p.Gln176Leu)
NM_006009.4(TUBA1A):c.528G>C (p.Gln176His)
NM_006009.4(TUBA1A):c.528G>T (p.Gln176His)
NM_006009.4(TUBA1A):c.53A>G (p.Asn18Ser) rs1064795213
NM_006009.4(TUBA1A):c.541G>A (p.Val181Ile)
NM_006009.4(TUBA1A):c.547G>A (p.Glu183Lys)
NM_006009.4(TUBA1A):c.562_564dup (p.Ile188dup) rs587784490
NM_006009.4(TUBA1A):c.578C>T (p.Thr193Ile)
NM_006009.4(TUBA1A):c.581C>T (p.Thr194Ile) rs1397581823
NM_006009.4(TUBA1A):c.638G>C (p.Cys213Ser) rs2121244232
NM_006009.4(TUBA1A):c.640C>A (p.Arg214Ser) rs886044568
NM_006009.4(TUBA1A):c.640C>T (p.Arg214Cys) rs886044568
NM_006009.4(TUBA1A):c.652G>A (p.Asp218Asn) rs1057517858
NM_006009.4(TUBA1A):c.661C>G (p.Arg221Gly)
NM_006009.4(TUBA1A):c.662G>A (p.Arg221His)
NM_006009.4(TUBA1A):c.680T>A (p.Leu227Gln) rs2121243965
NM_006009.4(TUBA1A):c.70T>C (p.Tyr24His)
NM_006009.4(TUBA1A):c.71A>G (p.Tyr24Cys) rs2121248469
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.790C>G (p.Arg264Gly) rs137853043
NM_006009.4(TUBA1A):c.791G>A (p.Arg264His) rs886043627
NM_006009.4(TUBA1A):c.791G>T (p.Arg264Leu)
NM_006009.4(TUBA1A):c.796C>T (p.His266Tyr)
NM_006009.4(TUBA1A):c.817G>A (p.Ala273Thr) rs1592259821
NM_006009.4(TUBA1A):c.82C>T (p.His28Tyr) rs1555162549
NM_006009.4(TUBA1A):c.870G>T (p.Glu290Asp)
NM_006009.4(TUBA1A):c.889G>A (p.Glu297Lys)
NM_006009.4(TUBA1A):c.937A>G (p.Met313Val)
NM_006009.4(TUBA1A):c.967G>A (p.Val323Met) rs2121242709
NM_006009.4(TUBA1A):c.983_984delinsAA (p.Val328Glu)
NM_006009.4(TUBA1A):c.991G>A (p.Ala331Thr) rs587784496
NM_006009.4(TUBA1A):c.995T>C (p.Ile332Thr) rs587784497

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