Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.59024107_59024109delCA2653535268TUBB1c.680_682del (p.His227del)
c.614_616del (p.His205del)
gnomAD v4
20g.59024106C>ACA409467433TUBB1c.679C>A (p.His227Asn)
c.613C>A (p.His205Asn)
20g.59024106C>GCA409467434TUBB1c.679C>G (p.His227Asp)
c.613C>G (p.His205Asp)
20g.59024106C>TCA409467435TUBB1c.679C>T (p.His227Tyr)
c.613C>T (p.His205Tyr)
20g.59024106_59024110delinsCACCTCA2372582071TUBB1c.679_683delinsCACCT (p.His227=)
c.613_617delinsCACCT (p.His205=)
20g.59024107A>CCA409467436TUBB1c.680A>C (p.His227Pro)
c.614A>C (p.His205Pro)
20g.59024107A>GCA409467437TUBB1c.680A>G (p.His227Arg)
c.614A>G (p.His205Arg)
20g.59024107A>TCA409467438TUBB1c.680A>T (p.His227Leu)
c.614A>T (p.His205Leu)
20g.59024108_59024111delCA636607945TUBB1c.681_684del (p.His227GlnfsTer4)
c.615_618del (p.His205GlnfsTer4)
dbSNP gnomAD v2 gnomAD v4
20g.59024108C>ACA409467439TUBB1c.681C>A (p.His227Gln)
c.615C>A (p.His205Gln)
20g.59024108C=CA2372582072TUBB1c.681C= (p.His227=)
c.615C= (p.His205=)
20g.59024108C>GCA409467440TUBB1c.681C>G (p.His227Gln)
c.615C>G (p.His205Gln)
gnomAD v4
20g.59024108C>TCA511316543TUBB1c.681C>T (p.His227=)
c.615C>T (p.His205=)
dbSNP
20g.59024109C>ACA409467441TUBB1c.682C>A (p.Leu228Ile)
c.616C>A (p.Leu206Ile)
20g.59024109C=CA2372582073TUBB1c.682C= (p.Leu228=)
c.616C= (p.Leu206=)
20g.59024109C>GCA409467442TUBB1c.682C>G (p.Leu228Val)
c.616C>G (p.Leu206Val)
dbSNP
20g.59024109C>TCA511316544TUBB1c.682C>T (p.Leu228=)
c.616C>T (p.Leu206=)
20g.59024110T>ACA409467444TUBB1c.683T>A (p.Leu228Gln)
c.617T>A (p.Leu206Gln)
COSMIC
20g.59024110T>CCA9928563TUBB1c.683T>C (p.Leu228Pro)
c.617T>C (p.Leu206Pro)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
20g.59024110T>GCA409467443TUBB1c.683T>G (p.Leu228Arg)
c.617T>G (p.Leu206Arg)
20g.59024110T=CA2372582074TUBB1c.683T= (p.Leu228=)
c.617T= (p.Leu206=)
20g.59024111A>CCA511316545TUBB1c.684A>C (p.Leu228=)
c.618A>C (p.Leu206=)
gnomAD v4
20g.59024111A>GCA511316546TUBB1c.684A>G (p.Leu228=)
c.618A>G (p.Leu206=)
ClinVar
20g.59024111A>TCA511316547TUBB1c.684A>T (p.Leu228=)
c.618A>T (p.Leu206=)
20g.59024112G>ACA409467445TUBB1c.685G>A (p.Val229Met)
c.619G>A (p.Val207Met)
20g.59024112G>CCA409467446TUBB1c.685G>C (p.Val229Leu)
c.619G>C (p.Val207Leu)
dbSNP gnomAD v3 gnomAD v4
20g.59024112G=CA2372582075TUBB1c.685G= (p.Val229=)
c.619G= (p.Val207=)
20g.59024112G>TCA409467447TUBB1c.685G>T (p.Val229Leu)
c.619G>T (p.Val207Leu)
20g.59024113T>ACA409467448TUBB1c.686T>A (p.Val229Glu)
c.620T>A (p.Val207Glu)
20g.59024113T>CCA409467449TUBB1c.686T>C (p.Val229Ala)
c.620T>C (p.Val207Ala)
gnomAD v4
20g.59024113T>GCA409467450TUBB1c.686T>G (p.Val229Gly)
c.620T>G (p.Val207Gly)
20g.59024114G>ACA511316550TUBB1c.687G>A (p.Val229=)
c.621G>A (p.Val207=)
gnomAD v4
20g.59024114G>CCA511316549TUBB1c.687G>C (p.Val229=)
c.621G>C (p.Val207=)
20g.59024114G>TCA511316548TUBB1c.687G>T (p.Val229=)
c.621G>T (p.Val207=)
20g.59024115T>ACA409467451TUBB1c.688T>A (p.Ser230Thr)
c.622T>A (p.Ser208Thr)
20g.59024115T>CCA409467452TUBB1c.688T>C (p.Ser230Pro)
c.622T>C (p.Ser208Pro)
gnomAD v4
20g.59024115T>GCA409467453TUBB1c.688T>G (p.Ser230Ala)
c.622T>G (p.Ser208Ala)
20g.59024116C>ACA409467454TUBB1c.689C>A (p.Ser230Tyr)
c.623C>A (p.Ser208Tyr)
20g.59024116C=CA2372582076TUBB1c.689C= (p.Ser230=)
c.623C= (p.Ser208=)
20g.59024116C>GCA409467455TUBB1c.689C>G (p.Ser230Cys)
c.623C>G (p.Ser208Cys)
20g.59024116C>TCA9928564TUBB1c.689C>T (p.Ser230Phe)
c.623C>T (p.Ser208Phe)
dbSNP ExAC gnomAD v2 gnomAD v4
20g.59024117C>ACA511316553TUBB1c.690C>A (p.Ser230=)
c.624C>A (p.Ser208=)
20g.59024117C>GCA511316555TUBB1c.690C>G (p.Ser230=)
c.624C>G (p.Ser208=)
20g.59024117C>TCA511316554TUBB1c.690C>T (p.Ser230=)
c.624C>T (p.Ser208=)
20g.59024118T>ACA409467457TUBB1c.691T>A (p.Leu231Met)
c.625T>A (p.Leu209Met)
20g.59024118T>CCA511316556TUBB1c.691T>C (p.Leu231=)
c.625T>C (p.Leu209=)
20g.59024118T>GCA409467456TUBB1c.691T>G (p.Leu231Val)
c.625T>G (p.Leu209Val)
20g.59024119T>ACA409467458TUBB1c.692T>A (p.Leu231Ter)
c.626T>A (p.Leu209Ter)
20g.59024119T>CCA409467460TUBB1c.692T>C (p.Leu231Ser)
c.626T>C (p.Leu209Ser)
20g.59024119T>GCA409467459TUBB1c.692T>G (p.Leu231Trp)
c.626T>G (p.Leu209Trp)

Number of alleles fetched