ClinVar Miner

List of variants in gene TUBA1A reported as uncertain significance for not provided

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Total variants: 54
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HGVS dbSNP gnomAD frequency
NM_006009.4(TUBA1A):c.4-7C>T rs560491477 0.00053
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.1127G>A (p.Cys376Tyr) rs2121241786
NM_006009.4(TUBA1A):c.1154C>T (p.Ala385Val)
NM_006009.4(TUBA1A):c.1225G>A (p.Val409Ile) rs1565626928
NM_006009.4(TUBA1A):c.1237A>T (p.Met413Leu) rs2121241343
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.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.250C>A (p.Arg84Ser)
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.326C>G (p.Thr109Ser) rs2121246504
NM_006009.4(TUBA1A):c.343A>T (p.Ile115Phe)
NM_006009.4(TUBA1A):c.362G>A (p.Arg121Gln) rs2121246284
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.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.449C>T (p.Thr150Ile) rs1565627339
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.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.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.652G>A (p.Asp218Asn) rs1057517858
NM_006009.4(TUBA1A):c.662G>A (p.Arg221His)
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.790C>G (p.Arg264Gly) rs137853043
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.870G>T (p.Glu290Asp)
NM_006009.4(TUBA1A):c.967G>A (p.Val323Met) rs2121242709
NM_006009.4(TUBA1A):c.983_984delinsAA (p.Val328Glu)

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