Chr Mutation (hg38) CAid Gene Transcript Linkouts
16g.89935135G>ACA497381078TUBB3c.684G>A (p.Leu228=)
n.4105G>A
c.468G>A (p.Leu156=)
c.277+1557G>A (n.277+1557G>A)
c.*769G>A (n.*769G>A)
c.1725G>A (p.Leu575=)
 gnomAD v4
16g.89935135G>CCA8256150TUBB3c.684G>C (p.Leu228=)
n.4105G>C
c.468G>C (p.Leu156=)
c.277+1557G>C (n.277+1557G>C)
c.*769G>C (n.*769G>C)
c.1725G>C (p.Leu575=)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
16g.89935135G=CA2242019952TUBB3c.684G= (p.Leu228=)
n.4105G=
c.468G= (p.Leu156=)
c.277+1557G= (n.277+1557G=)
c.*769G= (n.*769G=)
c.1725G= (p.Leu575=)
16g.89935135G>TCA497381080TUBB3c.684G>T (p.Leu228=)
n.4105G>T
c.468G>T (p.Leu156=)
c.277+1557G>T (n.277+1557G>T)
c.*769G>T (n.*769G>T)
c.1725G>T (p.Leu575=)
16g.89935136G>ACA397475116TUBB3c.685G>A (p.Val229Ile)
n.4106G>A
c.469G>A (p.Val157Ile)
c.277+1558G>A (n.277+1558G>A)
c.*770G>A (n.*770G>A)
c.1726G>A (p.Val576Ile)
16g.89935136G>CCA397475117TUBB3c.685G>C (p.Val229Leu)
n.4106G>C
c.469G>C (p.Val157Leu)
c.277+1558G>C (n.277+1558G>C)
c.*770G>C (n.*770G>C)
c.1726G>C (p.Val576Leu)
16g.89935136G>TCA397475118TUBB3c.685G>T (p.Val229Leu)
n.4106G>T
c.469G>T (p.Val157Leu)
c.277+1558G>T (n.277+1558G>T)
c.*770G>T (n.*770G>T)
c.1726G>T (p.Val576Leu)
16g.89935137T>ACA397475119TUBB3c.686T>A (p.Val229Glu)
n.4107T>A
c.470T>A (p.Val157Glu)
c.277+1559T>A (n.277+1559T>A)
c.*771T>A (n.*771T>A)
c.1727T>A (p.Val576Glu)
16g.89935137T>CCA397475120TUBB3c.686T>C (p.Val229Ala)
n.4107T>C
c.470T>C (p.Val157Ala)
c.277+1559T>C (n.277+1559T>C)
c.*771T>C (n.*771T>C)
c.1727T>C (p.Val576Ala)
16g.89935137T>GCA397475121TUBB3c.686T>G (p.Val229Gly)
n.4107T>G
c.470T>G (p.Val157Gly)
c.277+1559T>G (n.277+1559T>G)
c.*771T>G (n.*771T>G)
c.1727T>G (p.Val576Gly)
16g.89935138A=CA2242019959TUBB3c.687A= (p.Val229=)
n.4108A=
c.471A= (p.Val157=)
c.277+1560A= (n.277+1560A=)
c.*772A= (n.*772A=)
c.1728A= (p.Val576=)
16g.89935138A>CCA497381083TUBB3c.687A>C (p.Val229=)
n.4108A>C
c.471A>C (p.Val157=)
c.277+1560A>C (n.277+1560A>C)
c.*772A>C (n.*772A>C)
c.1728A>C (p.Val576=)
16g.89935138A>GCA286619078TUBB3c.687A>G (p.Val229=)
n.4108A>G
c.471A>G (p.Val157=)
c.277+1560A>G (n.277+1560A>G)
c.*772A>G (n.*772A>G)
c.1728A>G (p.Val576=)
 dbSNP gnomAD v3 gnomAD v4
16g.89935138A>TCA8256151TUBB3c.687A>T (p.Val229=)
n.4108A>T
c.471A>T (p.Val157=)
c.277+1560A>T (n.277+1560A>T)
c.*772A>T (n.*772A>T)
c.1728A>T (p.Val576=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.89935139T>ACA397475124TUBB3c.688T>A (p.Ser230Thr)
n.4109T>A
c.472T>A (p.Ser158Thr)
c.277+1561T>A (n.277+1561T>A)
c.*773T>A (n.*773T>A)
c.1729T>A (p.Ser577Thr)
16g.89935139T>CCA397475123TUBB3c.688T>C (p.Ser230Pro)
n.4109T>C
c.472T>C (p.Ser158Pro)
c.277+1561T>C (n.277+1561T>C)
c.*773T>C (n.*773T>C)
c.1729T>C (p.Ser577Pro)
16g.89935139T>GCA397475122TUBB3c.688T>G (p.Ser230Ala)
n.4109T>G
c.472T>G (p.Ser158Ala)
c.277+1561T>G (n.277+1561T>G)
c.*773T>G (n.*773T>G)
c.1729T>G (p.Ser577Ala)
16g.89935140C>ACA397475125TUBB3c.689C>A (p.Ser230Ter)
n.4110C>A
c.473C>A (p.Ser158Ter)
c.277+1562C>A (n.277+1562C>A)
c.*774C>A (n.*774C>A)
c.1730C>A (p.Ser577Ter)
16g.89935140C=CA2242019967TUBB3c.689C= (p.Ser230=)
n.4110C=
c.473C= (p.Ser158=)
c.277+1562C= (n.277+1562C=)
c.*774C= (n.*774C=)
c.1730C= (p.Ser577=)
16g.89935140C>GCA397475126TUBB3c.689C>G (p.Ser230Trp)
n.4110C>G
c.473C>G (p.Ser158Trp)
c.277+1562C>G (n.277+1562C>G)
c.*774C>G (n.*774C>G)
c.1730C>G (p.Ser577Trp)
16g.89935140C>TCA10603568TUBB3c.689C>T (p.Ser230Leu)
n.4110C>T
c.473C>T (p.Ser158Leu)
c.277+1562C>T (n.277+1562C>T)
c.*774C>T (n.*774C>T)
c.1730C>T (p.Ser577Leu)
 ClinVar dbSNP
16g.89935141G>ACA8256152TUBB3c.690G>A (p.Ser230=)
n.4111G>A
c.474G>A (p.Ser158=)
c.277+1563G>A (n.277+1563G>A)
c.*775G>A (n.*775G>A)
c.1731G>A (p.Ser577=)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
16g.89935141G>CCA497381089TUBB3c.690G>C (p.Ser230=)
n.4111G>C
c.474G>C (p.Ser158=)
c.277+1563G>C (n.277+1563G>C)
c.*775G>C (n.*775G>C)
c.1731G>C (p.Ser577=)
16g.89935141G=CA2242019971TUBB3c.690G= (p.Ser230=)
n.4111G=
c.474G= (p.Ser158=)
c.277+1563G= (n.277+1563G=)
c.*775G= (n.*775G=)
c.1731G= (p.Ser577=)
16g.89935141G>TCA497381088TUBB3c.690G>T (p.Ser230=)
n.4111G>T
c.474G>T (p.Ser158=)
c.277+1563G>T (n.277+1563G>T)
c.*775G>T (n.*775G>T)
c.1731G>T (p.Ser577=)
16g.89935142G>ACA397475127TUBB3c.691G>A (p.Ala231Thr)
n.4112G>A
c.475G>A (p.Ala159Thr)
c.277+1564G>A (n.277+1564G>A)
c.*776G>A (n.*776G>A)
c.1732G>A (p.Ala578Thr)
16g.89935142G>CCA397475128TUBB3c.691G>C (p.Ala231Pro)
n.4112G>C
c.475G>C (p.Ala159Pro)
c.277+1564G>C (n.277+1564G>C)
c.*776G>C (n.*776G>C)
c.1732G>C (p.Ala578Pro)
16g.89935142G>TCA397475129TUBB3c.691G>T (p.Ala231Ser)
n.4112G>T
c.475G>T (p.Ala159Ser)
c.277+1564G>T (n.277+1564G>T)
c.*776G>T (n.*776G>T)
c.1732G>T (p.Ala578Ser)
16g.89935143C>ACA397475130TUBB3c.692C>A (p.Ala231Asp)
n.4113C>A
c.476C>A (p.Ala159Asp)
c.277+1565C>A (n.277+1565C>A)
c.*777C>A (n.*777C>A)
c.1733C>A (p.Ala578Asp)
16g.89935143C=CA2242019975TUBB3c.692C= (p.Ala231=)
n.4113C=
c.476C= (p.Ala159=)
c.277+1565C= (n.277+1565C=)
c.*777C= (n.*777C=)
c.1733C= (p.Ala578=)
16g.89935143C>GCA397475131TUBB3c.692C>G (p.Ala231Gly)
n.4113C>G
c.476C>G (p.Ala159Gly)
c.277+1565C>G (n.277+1565C>G)
c.*777C>G (n.*777C>G)
c.1733C>G (p.Ala578Gly)
 dbSNP
16g.89935143C>TCA397475132TUBB3c.692C>T (p.Ala231Val)
n.4113C>T
c.476C>T (p.Ala159Val)
c.277+1565C>T (n.277+1565C>T)
c.*777C>T (n.*777C>T)
c.1733C>T (p.Ala578Val)
16g.89935144C>ACA8256153TUBB3c.693C>A (p.Ala231=)
n.4114C>A
c.477C>A (p.Ala159=)
c.277+1566C>A (n.277+1566C>A)
c.*778C>A (n.*778C>A)
c.1734C>A (p.Ala578=)
 dbSNP ExAC gnomAD v2 gnomAD v4
16g.89935144C=CA2242019977TUBB3c.693C= (p.Ala231=)
n.4114C=
c.477C= (p.Ala159=)
c.277+1566C= (n.277+1566C=)
c.*778C= (n.*778C=)
c.1734C= (p.Ala578=)
16g.89935144C>GCA497381093TUBB3c.693C>G (p.Ala231=)
n.4114C>G
c.477C>G (p.Ala159=)
c.277+1566C>G (n.277+1566C>G)
c.*778C>G (n.*778C>G)
c.1734C>G (p.Ala578=)
16g.89935144C>TCA497381095TUBB3c.693C>T (p.Ala231=)
n.4114C>T
c.477C>T (p.Ala159=)
c.277+1566C>T (n.277+1566C>T)
c.*778C>T (n.*778C>T)
c.1734C>T (p.Ala578=)
 gnomAD v4
16g.89935145A>CCA397475133TUBB3c.694A>C (p.Thr232Pro)
n.4115A>C
c.478A>C (p.Thr160Pro)
c.277+1567A>C (n.277+1567A>C)
c.*779A>C (n.*779A>C)
c.1735A>C (p.Thr579Pro)
16g.89935145A>GCA397475134TUBB3c.694A>G (p.Thr232Ala)
n.4115A>G
c.478A>G (p.Thr160Ala)
c.277+1567A>G (n.277+1567A>G)
c.*779A>G (n.*779A>G)
c.1735A>G (p.Thr579Ala)
16g.89935145A>TCA397475135TUBB3c.694A>T (p.Thr232Ser)
n.4115A>T
c.478A>T (p.Thr160Ser)
c.277+1567A>T (n.277+1567A>T)
c.*779A>T (n.*779A>T)
c.1735A>T (p.Thr579Ser)
16g.89935146C>ACA397475138TUBB3c.695C>A (p.Thr232Asn)
n.4116C>A
c.479C>A (p.Thr160Asn)
c.277+1568C>A (n.277+1568C>A)
c.*780C>A (n.*780C>A)
c.1736C>A (p.Thr579Asn)
16g.89935146C>GCA397475137TUBB3c.695C>G (p.Thr232Ser)
n.4116C>G
c.479C>G (p.Thr160Ser)
c.277+1568C>G (n.277+1568C>G)
c.*780C>G (n.*780C>G)
c.1736C>G (p.Thr579Ser)
16g.89935146C>TCA397475136TUBB3c.695C>T (p.Thr232Ile)
n.4116C>T
c.479C>T (p.Thr160Ile)
c.277+1568C>T (n.277+1568C>T)
c.*780C>T (n.*780C>T)
c.1736C>T (p.Thr579Ile)
16g.89935147C>ACA497381098TUBB3c.696C>A (p.Thr232=)
n.4117C>A
c.480C>A (p.Thr160=)
c.277+1569C>A (n.277+1569C>A)
c.*781C>A (n.*781C>A)
c.1737C>A (p.Thr579=)
16g.89935147C>GCA497381099TUBB3c.696C>G (p.Thr232=)
n.4117C>G
c.480C>G (p.Thr160=)
c.277+1569C>G (n.277+1569C>G)
c.*781C>G (n.*781C>G)
c.1737C>G (p.Thr579=)
 gnomAD v4
16g.89935147C>TCA497381100TUBB3c.696C>T (p.Thr232=)
n.4117C>T
c.480C>T (p.Thr160=)
c.277+1569C>T (n.277+1569C>T)
c.*781C>T (n.*781C>T)
c.1737C>T (p.Thr579=)
 COSMIC
16g.89935148A>CCA397475139TUBB3c.697A>C (p.Met233Leu)
n.4118A>C
c.481A>C (p.Met161Leu)
c.277+1570A>C (n.277+1570A>C)
c.*782A>C (n.*782A>C)
c.1738A>C (p.Met580Leu)
16g.89935148A>GCA397475140TUBB3c.697A>G (p.Met233Val)
n.4118A>G
c.481A>G (p.Met161Val)
c.277+1570A>G (n.277+1570A>G)
c.*782A>G (n.*782A>G)
c.1738A>G (p.Met580Val)
16g.89935148A>TCA397475141TUBB3c.697A>T (p.Met233Leu)
n.4118A>T
c.481A>T (p.Met161Leu)
c.277+1570A>T (n.277+1570A>T)
c.*782A>T (n.*782A>T)
c.1738A>T (p.Met580Leu)
16g.89935149T>ACA397475142TUBB3c.698T>A (p.Met233Lys)
n.4119T>A
c.482T>A (p.Met161Lys)
c.277+1571T>A (n.277+1571T>A)
c.*783T>A (n.*783T>A)
c.1739T>A (p.Met580Lys)
 gnomAD v4
16g.89935149T>CCA397475143TUBB3c.698T>C (p.Met233Thr)
n.4119T>C
c.482T>C (p.Met161Thr)
c.277+1571T>C (n.277+1571T>C)
c.*783T>C (n.*783T>C)
c.1739T>C (p.Met580Thr)

Number of alleles fetched