ClinVar Miner

List of variants in gene TUBA1A reported as likely benign by Invitae

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Total variants: 67
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HGVS dbSNP gnomAD frequency
NM_006009.4(TUBA1A):c.288A>G (p.Lys96=) rs1056875 0.45696
NM_006009.4(TUBA1A):c.1008G>A (p.Lys336=) rs11829764 0.00853
NM_006009.4(TUBA1A):c.786T>C (p.Tyr262=) rs762008241 0.00096
NM_006009.4(TUBA1A):c.227-17C>G rs367632910 0.00030
NM_006009.4(TUBA1A):c.390G>C (p.Thr130=) rs1143559 0.00018
NM_006009.4(TUBA1A):c.378C>T (p.Ala126=) rs1135224 0.00014
NM_006009.4(TUBA1A):c.96C>T (p.Pro32=) rs139102191 0.00011
NM_006009.4(TUBA1A):c.819C>T (p.Ala273=) rs140795162 0.00006
NM_006009.4(TUBA1A):c.1347G>A (p.Glu449=) rs200873943 0.00004
NM_006009.4(TUBA1A):c.24C>T (p.His8=) rs143047732 0.00004
NM_006009.4(TUBA1A):c.849T>C (p.His283=) rs759228609 0.00004
NM_006009.4(TUBA1A):c.330T>C (p.Ile110=) rs774370656 0.00003
NM_006009.4(TUBA1A):c.4-4A>G rs1280504729 0.00003
NM_006009.4(TUBA1A):c.651C>T (p.Leu217=) rs779416899 0.00003
NM_006009.4(TUBA1A):c.1071C>T (p.Tyr357=) rs1489213862 0.00001
NM_006009.4(TUBA1A):c.1227T>G (p.Val409=) rs766135902 0.00001
NM_006009.4(TUBA1A):c.168G>A (p.Thr56=) rs1215478236 0.00001
NM_006009.4(TUBA1A):c.190C>A (p.Arg64=) rs1064794568 0.00001
NM_006009.4(TUBA1A):c.952T>C (p.Leu318=) rs771520376 0.00001
NM_006009.4(TUBA1A):c.954G>A (p.Leu318=) rs17123567 0.00001
NM_006009.4(TUBA1A):c.1023C>T (p.Ile341=)
NM_006009.4(TUBA1A):c.1035T>C (p.Asp345=)
NM_006009.4(TUBA1A):c.1167T>C (p.Ala389=)
NM_006009.4(TUBA1A):c.1224C>T (p.Tyr408=)
NM_006009.4(TUBA1A):c.1230G>C (p.Gly410=) rs772809398
NM_006009.4(TUBA1A):c.1230G>T (p.Gly410=) rs772809398
NM_006009.4(TUBA1A):c.1263C>T (p.Ala421=) rs11558070
NM_006009.4(TUBA1A):c.132A>T (p.Gly44=)
NM_006009.4(TUBA1A):c.141T>C (p.Asp47=)
NM_006009.4(TUBA1A):c.192G>A (p.Arg64=)
NM_006009.4(TUBA1A):c.198G>A (p.Val66=)
NM_006009.4(TUBA1A):c.226+14A>C
NM_006009.4(TUBA1A):c.226+15G>A
NM_006009.4(TUBA1A):c.227-12C>G
NM_006009.4(TUBA1A):c.227-19C>T
NM_006009.4(TUBA1A):c.238A>T (p.Thr80Ser)
NM_006009.4(TUBA1A):c.276T>C (p.Leu92=) rs1065671
NM_006009.4(TUBA1A):c.291A>G (p.Glu97=)
NM_006009.4(TUBA1A):c.3+20C>T
NM_006009.4(TUBA1A):c.3+9C>A rs1592261624
NM_006009.4(TUBA1A):c.324C>T (p.Tyr108=) rs1236410746
NM_006009.4(TUBA1A):c.375+12T>C
NM_006009.4(TUBA1A):c.376-4A>G
NM_006009.4(TUBA1A):c.376-9T>C
NM_006009.4(TUBA1A):c.378C>G (p.Ala126=)
NM_006009.4(TUBA1A):c.384G>A (p.Gln128=)
NM_006009.4(TUBA1A):c.399G>A (p.Gln133=) rs1942175208
NM_006009.4(TUBA1A):c.4-18C>G
NM_006009.4(TUBA1A):c.4-8C>G
NM_006009.4(TUBA1A):c.438T>G (p.Gly146=)
NM_006009.4(TUBA1A):c.453G>A (p.Ser151=)
NM_006009.4(TUBA1A):c.492G>A (p.Lys164=)
NM_006009.4(TUBA1A):c.519G>A (p.Pro173=)
NM_006009.4(TUBA1A):c.525C>T (p.Pro175=)
NM_006009.4(TUBA1A):c.543A>G (p.Val181=)
NM_006009.4(TUBA1A):c.567C>T (p.Leu189=)
NM_006009.4(TUBA1A):c.576C>T (p.His192=)
NM_006009.4(TUBA1A):c.630T>C (p.Tyr210=)
NM_006009.4(TUBA1A):c.657T>C (p.Ile219=)
NM_006009.4(TUBA1A):c.675T>C (p.Thr225=)
NM_006009.4(TUBA1A):c.687G>A (p.Arg229=)
NM_006009.4(TUBA1A):c.753C>T (p.Asp251=)
NM_006009.4(TUBA1A):c.762A>G (p.Glu254=)
NM_006009.4(TUBA1A):c.780G>A (p.Val260=)
NM_006009.4(TUBA1A):c.882T>A (p.Ala294=)
NM_006009.4(TUBA1A):c.930T>G (p.Gly310=)
NM_006009.4(TUBA1A):c.942T>C (p.Ala314=)

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