Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
9g.130862877A>CCA375262696ABL1c.721A>C (p.Lys241Gln)
c.664A>C (p.Lys222Gln)
9g.130862877A>GCA375262698ABL1c.721A>G (p.Lys241Glu)
c.664A>G (p.Lys222Glu)
9g.130862877A>TCA375262694ABL1c.721A>T (p.Lys241Ter)
c.664A>T (p.Lys222Ter)
9g.130862878A>CCA375262701ABL1c.722A>C (p.Lys241Thr)
c.665A>C (p.Lys222Thr)
9g.130862878A>GCA375262705ABL1c.722A>G (p.Lys241Arg)
c.665A>G (p.Lys222Arg)
9g.130862878A>TCA375262703ABL1c.722A>T (p.Lys241Met)
c.665A>T (p.Lys222Met)
dbSNP
9g.130862879G>ACA467496260ABL1c.723G>A (p.Lys241=)
c.666G>A (p.Lys222=)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862879G>CCA375262708ABL1c.723G>C (p.Lys241Asn)
c.666G>C (p.Lys222Asn)
dbSNP
9g.130862879G=CA1881463189ABL1c.723G= (p.Lys241=)
c.666G= (p.Lys222=)
9g.130862879G>TCA375262710ABL1c.723G>T (p.Lys241Asn)
c.666G>T (p.Lys222Asn)
9g.130862880C>ACA375262713ABL1c.724C>A (p.Pro242Thr)
c.667C>A (p.Pro223Thr)
dbSNP
9g.130862880C>GCA375262716ABL1c.724C>G (p.Pro242Ala)
c.667C>G (p.Pro223Ala)
9g.130862880C>TCA375262719ABL1c.724C>T (p.Pro242Ser)
c.667C>T (p.Pro223Ser)
dbSNP
9g.130862881C>ACA375262722ABL1c.725C>A (p.Pro242His)
c.668C>A (p.Pro223His)
9g.130862881C>GCA375262724ABL1c.725C>G (p.Pro242Arg)
c.668C>G (p.Pro223Arg)
9g.130862881C>TCA375262726ABL1c.725C>T (p.Pro242Leu)
c.668C>T (p.Pro223Leu)
9g.130862882C>ACA467496264ABL1c.726C>A (p.Pro242=)
c.669C>A (p.Pro223=)
9g.130862882C=CA1881463195ABL1c.726C= (p.Pro242=)
c.669C= (p.Pro223=)
9g.130862882C>GCA467496266ABL1c.726C>G (p.Pro242=)
c.669C>G (p.Pro223=)
9g.130862882C>TCA467496265ABL1c.726C>T (p.Pro242=)
c.669C>T (p.Pro223=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862883A>CCA375262729ABL1c.727A>C (p.Thr243Pro)
c.670A>C (p.Thr224Pro)
9g.130862883A>GCA375262731ABL1c.727A>G (p.Thr243Ala)
c.670A>G (p.Thr224Ala)
gnomAD v4
9g.130862883A>TCA375262734ABL1c.727A>T (p.Thr243Ser)
c.670A>T (p.Thr224Ser)
dbSNP
9g.130862884C>ACA375262741ABL1c.728C>A (p.Thr243Asn)
c.671C>A (p.Thr224Asn)
9g.130862884C>GCA375262739ABL1c.728C>G (p.Thr243Ser)
c.671C>G (p.Thr224Ser)
9g.130862884C>TCA375262737ABL1c.728C>T (p.Thr243Ile)
c.671C>T (p.Thr224Ile)
dbSNP
9g.130862885T>ACA467496269ABL1c.729T>A (p.Thr243=)
c.672T>A (p.Thr224=)
9g.130862885T>CCA5285268ABL1c.729T>C (p.Thr243=)
c.672T>C (p.Thr224=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862885T>GCA467496271ABL1c.729T>G (p.Thr243=)
c.672T>G (p.Thr224=)
gnomAD v4
9g.130862885T=CA1881463199ABL1c.729T= (p.Thr243=)
c.672T= (p.Thr224=)
9g.130862886G>ACA375262747ABL1c.730G>A (p.Val244Ile)
c.673G>A (p.Val225Ile)
9g.130862886G>CCA375262749ABL1c.730G>C (p.Val244Leu)
c.673G>C (p.Val225Leu)
9g.130862886G>TCA375262751ABL1c.730G>T (p.Val244Phe)
c.673G>T (p.Val225Phe)
9g.130862887T>ACA375262755ABL1c.731T>A (p.Val244Asp)
c.674T>A (p.Val225Asp)
9g.130862887T>CCA375262757ABL1c.731T>C (p.Val244Ala)
c.674T>C (p.Val225Ala)
ClinVar dbSNP
9g.130862887T>GCA375262758ABL1c.731T>G (p.Val244Gly)
c.674T>G (p.Val225Gly)
9g.130862887T=CA1881463210ABL1c.731T= (p.Val244=)
c.674T= (p.Val225=)
9g.130862888C>ACA467496274ABL1c.732C>A (p.Val244=)
c.675C>A (p.Val225=)
9g.130862888C>GCA467496276ABL1c.732C>G (p.Val244=)
c.675C>G (p.Val225=)
9g.130862888C>TCA467496278ABL1c.732C>T (p.Val244=)
c.675C>T (p.Val225=)
9g.130862889T>ACA375262760ABL1c.733T>A (p.Tyr245Asn)
c.676T>A (p.Tyr226Asn)
9g.130862889T>CCA375262762ABL1c.733T>C (p.Tyr245His)
c.676T>C (p.Tyr226His)
9g.130862889T>GCA375262764ABL1c.733T>G (p.Tyr245Asp)
c.676T>G (p.Tyr226Asp)
9g.130862890A=CA1881463220ABL1c.734A= (p.Tyr245=)
c.677A= (p.Tyr226=)
9g.130862890A>CCA375262767ABL1c.734A>C (p.Tyr245Ser)
c.677A>C (p.Tyr226Ser)
9g.130862890A>GCA16609342ABL1c.734A>G (p.Tyr245Cys)
c.677A>G (p.Tyr226Cys)
ClinVar dbSNP
9g.130862890A>TCA375262770ABL1c.734A>T (p.Tyr245Phe)
c.677A>T (p.Tyr226Phe)
9g.130862891T>ACA375262772ABL1c.735T>A (p.Tyr245Ter)
c.678T>A (p.Tyr226Ter)
9g.130862891T>CCA467496281ABL1c.735T>C (p.Tyr245=)
c.678T>C (p.Tyr226=)
dbSNP
9g.130862891T>GCA375262774ABL1c.735T>G (p.Tyr245Ter)
c.678T>G (p.Tyr226Ter)
9g.130862892G>ACA375262778ABL1c.736G>A (p.Gly246Ser)
c.679G>A (p.Gly227Ser)
dbSNP
9g.130862892G>CCA375262779ABL1c.736G>C (p.Gly246Arg)
c.679G>C (p.Gly227Arg)
9g.130862892G>TCA375262781ABL1c.736G>T (p.Gly246Cys)
c.679G>T (p.Gly227Cys)
9g.130862893G>ACA375262784ABL1c.737G>A (p.Gly246Asp)
c.680G>A (p.Gly227Asp)
dbSNP gnomAD v4
9g.130862893G>CCA375262787ABL1c.737G>C (p.Gly246Ala)
c.680G>C (p.Gly227Ala)
dbSNP
9g.130862893G=CA1881463228ABL1c.737G= (p.Gly246=)
c.680G= (p.Gly227=)
9g.130862893G>TCA375262789ABL1c.737G>T (p.Gly246Val)
c.680G>T (p.Gly227Val)
9g.130862894T>ACA467496286ABL1c.738T>A (p.Gly246=)
c.681T>A (p.Gly227=)
9g.130862894T>CCA467496287ABL1c.738T>C (p.Gly246=)
c.681T>C (p.Gly227=)
gnomAD v4
9g.130862894T>GCA467496288ABL1c.738T>G (p.Gly246=)
c.681T>G (p.Gly227=)
gnomAD v4
9g.130862895G>ACA375262792ABL1c.739G>A (p.Val247Met)
c.682G>A (p.Val228Met)
dbSNP
9g.130862895G>CCA375262794ABL1c.739G>C (p.Val247Leu)
c.682G>C (p.Val228Leu)
dbSNP
9g.130862895G=CA1881463234ABL1c.739G= (p.Val247=)
c.682G= (p.Val228=)
9g.130862895G>TCA375262796ABL1c.739G>T (p.Val247Leu)
c.682G>T (p.Val228Leu)
9g.130862895_130862896insCCA590945364ABL1c.739_740insC (p.Val247AlafsTer?)
c.682_683insC (p.Val228AlafsTer?)
dbSNP gnomAD v2
9g.130862896T>ACA375262799ABL1c.740T>A (p.Val247Glu)
c.683T>A (p.Val228Glu)
9g.130862896T>CCA375262801ABL1c.740T>C (p.Val247Ala)
c.683T>C (p.Val228Ala)
9g.130862896T>GCA375262803ABL1c.740T>G (p.Val247Gly)
c.683T>G (p.Val228Gly)
9g.130862897G>ACA467496292ABL1c.741G>A (p.Val247=)
c.684G>A (p.Val228=)
dbSNP
9g.130862897G>CCA467496294ABL1c.741G>C (p.Val247=)
c.684G>C (p.Val228=)
9g.130862897G>TCA467496296ABL1c.741G>T (p.Val247=)
c.684G>T (p.Val228=)
9g.130862898T>ACA375262808ABL1c.742T>A (p.Ser248Thr)
c.685T>A (p.Ser229Thr)
9g.130862898T>CCA375262810ABL1c.742T>C (p.Ser248Pro)
c.685T>C (p.Ser229Pro)
dbSNP
9g.130862898T>GCA375262806ABL1c.742T>G (p.Ser248Ala)
c.685T>G (p.Ser229Ala)
9g.130862899C>ACA375262813ABL1c.743C>A (p.Ser248Tyr)
c.686C>A (p.Ser229Tyr)
gnomAD v4
9g.130862899C>GCA375262815ABL1c.743C>G (p.Ser248Cys)
c.686C>G (p.Ser229Cys)
9g.130862899C>TCA375262818ABL1c.743C>T (p.Ser248Phe)
c.686C>T (p.Ser229Phe)
9g.130862900C>ACA467496297ABL1c.744C>A (p.Ser248=)
c.687C>A (p.Ser229=)
9g.130862900C=CA1881463243ABL1c.744C= (p.Ser248=)
c.687C= (p.Ser229=)
9g.130862900C>GCA467496298ABL1c.744C>G (p.Ser248=)
c.687C>G (p.Ser229=)
9g.130862900C>TCA467496299ABL1c.744C>T (p.Ser248=)
c.687C>T (p.Ser229=)
dbSNP
9g.130862901C>ACA375262821ABL1c.745C>A (p.Pro249Thr)
c.688C>A (p.Pro230Thr)
9g.130862901C>GCA375262823ABL1c.745C>G (p.Pro249Ala)
c.688C>G (p.Pro230Ala)
9g.130862901C>TCA375262825ABL1c.745C>T (p.Pro249Ser)
c.688C>T (p.Pro230Ser)
9g.130862902C>ACA375262827ABL1c.746C>A (p.Pro249His)
c.689C>A (p.Pro230His)
9g.130862902C=CA1881463254ABL1c.746C= (p.Pro249=)
c.689C= (p.Pro230=)
9g.130862902C>GCA375262832ABL1c.746C>G (p.Pro249Arg)
c.689C>G (p.Pro230Arg)
9g.130862902C>TCA375262830ABL1c.746C>T (p.Pro249Leu)
c.689C>T (p.Pro230Leu)
ClinVar dbSNP
9g.130862903C>ACA200680480ABL1c.747C>A (p.Pro249=)
c.690C>A (p.Pro230=)
dbSNP gnomAD v4
9g.130862903C=CA1881463262ABL1c.747C= (p.Pro249=)
c.690C= (p.Pro230=)
9g.130862903C>GCA467496301ABL1c.747C>G (p.Pro249=)
c.690C>G (p.Pro230=)
gnomAD v4
9g.130862903C>TCA467496300ABL1c.747C>T (p.Pro249=)
c.690C>T (p.Pro230=)
9g.130862904A=CA1881463266ABL1c.748A= (p.Asn250=)
c.691A= (p.Asn231=)
9g.130862904A>CCA375262837ABL1c.748A>C (p.Asn250His)
c.691A>C (p.Asn231His)
9g.130862904A>GCA375262839ABL1c.748A>G (p.Asn250Asp)
c.691A>G (p.Asn231Asp)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862904A>TCA375262842ABL1c.748A>T (p.Asn250Tyr)
c.691A>T (p.Asn231Tyr)
9g.130862905A=CA1881463276ABL1c.749A= (p.Asn250=)
c.692A= (p.Asn231=)
9g.130862905A>CCA375262844ABL1c.749A>C (p.Asn250Thr)
c.692A>C (p.Asn231Thr)
9g.130862905A>GCA5285269ABL1c.749A>G (p.Asn250Ser)
c.692A>G (p.Asn231Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862905A>TCA375262847ABL1c.749A>T (p.Asn250Ile)
c.692A>T (p.Asn231Ile)
9g.130862906C>ACA375262850ABL1c.750C>A (p.Asn250Lys)
c.693C>A (p.Asn231Lys)
9g.130862906C=CA1881463285ABL1c.750C= (p.Asn250=)
c.693C= (p.Asn231=)
9g.130862906C>GCA375262851ABL1c.750C>G (p.Asn250Lys)
c.693C>G (p.Asn231Lys)
gnomAD v4
9g.130862906C>TCA467496302ABL1c.750C>T (p.Asn250=)
c.693C>T (p.Asn231=)
dbSNP gnomAD v2 gnomAD v4
9g.130862907T>ACA375262855ABL1c.751T>A (p.Tyr251Asn)
c.694T>A (p.Tyr232Asn)
9g.130862907T>CCA375262859ABL1c.751T>C (p.Tyr251His)
c.694T>C (p.Tyr232His)
gnomAD v4
9g.130862907T>GCA375262857ABL1c.751T>G (p.Tyr251Asp)
c.694T>G (p.Tyr232Asp)
9g.130862908A>CCA375262862ABL1c.752A>C (p.Tyr251Ser)
c.695A>C (p.Tyr232Ser)
9g.130862908A>GCA375262864ABL1c.752A>G (p.Tyr251Cys)
c.695A>G (p.Tyr232Cys)
9g.130862908A>TCA375262866ABL1c.752A>T (p.Tyr251Phe)
c.695A>T (p.Tyr232Phe)
dbSNP
9g.130862909C>ACA375262869ABL1c.753C>A (p.Tyr251Ter)
c.696C>A (p.Tyr232Ter)
9g.130862909C=CA1881463288ABL1c.753C= (p.Tyr251=)
c.696C= (p.Tyr232=)
9g.130862909C>GCA375262871ABL1c.753C>G (p.Tyr251Ter)
c.696C>G (p.Tyr232Ter)
9g.130862909C>TCA467496303ABL1c.753C>T (p.Tyr251=)
c.696C>T (p.Tyr232=)
dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862910G>ACA375262874ABL1c.754G>A (p.Asp252Asn)
c.697G>A (p.Asp233Asn)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862910G>CCA375262876ABL1c.754G>C (p.Asp252His)
c.697G>C (p.Asp233His)
9g.130862910G=CA1881463290ABL1c.754G= (p.Asp252=)
c.697G= (p.Asp233=)
9g.130862910G>TCA375262878ABL1c.754G>T (p.Asp252Tyr)
c.697G>T (p.Asp233Tyr)
9g.130862911A>CCA375262881ABL1c.755A>C (p.Asp252Ala)
c.698A>C (p.Asp233Ala)
dbSNP
9g.130862911A>GCA375262882ABL1c.755A>G (p.Asp252Gly)
c.698A>G (p.Asp233Gly)
9g.130862911A>TCA375262884ABL1c.755A>T (p.Asp252Val)
c.698A>T (p.Asp233Val)
9g.130862912C>ACA375262888ABL1c.756C>A (p.Asp252Glu)
c.699C>A (p.Asp233Glu)
9g.130862912C>GCA375262886ABL1c.756C>G (p.Asp252Glu)
c.699C>G (p.Asp233Glu)
9g.130862912C>TCA467496307ABL1c.756C>T (p.Asp252=)
c.699C>T (p.Asp233=)
9g.130862913A>CCA375262892ABL1c.757A>C (p.Lys253Gln)
c.700A>C (p.Lys234Gln)
gnomAD v4
9g.130862913A>GCA375262894ABL1c.757A>G (p.Lys253Glu)
c.700A>G (p.Lys234Glu)
9g.130862913A>TCA375262896ABL1c.757A>T (p.Lys253Ter)
c.700A>T (p.Lys234Ter)
9g.130862914A>CCA375262899ABL1c.758A>C (p.Lys253Thr)
c.701A>C (p.Lys234Thr)
9g.130862914A>GCA375262901ABL1c.758A>G (p.Lys253Arg)
c.701A>G (p.Lys234Arg)
9g.130862914A>TCA375262904ABL1c.758A>T (p.Lys253Met)
c.701A>T (p.Lys234Met)
9g.130862915G>ACA467496308ABL1c.759G>A (p.Lys253=)
c.702G>A (p.Lys234=)
9g.130862915G>CCA375262906ABL1c.759G>C (p.Lys253Asn)
c.702G>C (p.Lys234Asn)
9g.130862915G>TCA375262908ABL1c.759G>T (p.Lys253Asn)
c.702G>T (p.Lys234Asn)
9g.130862916T>ACA375262910ABL1c.760T>A (p.Trp254Arg)
c.703T>A (p.Trp235Arg)
dbSNP
9g.130862916T>CCA375262912ABL1c.760T>C (p.Trp254Arg)
c.703T>C (p.Trp235Arg)
9g.130862916T>GCA375262914ABL1c.760T>G (p.Trp254Gly)
c.703T>G (p.Trp235Gly)
9g.130862917G>ACA375262919ABL1c.761G>A (p.Trp254Ter)
c.704G>A (p.Trp235Ter)
9g.130862917G>CCA375262920ABL1c.761G>C (p.Trp254Ser)
c.704G>C (p.Trp235Ser)
9g.130862917G>TCA375262917ABL1c.761G>T (p.Trp254Leu)
c.704G>T (p.Trp235Leu)
9g.130862918G>ACA375262924ABL1c.762G>A (p.Trp254Ter)
c.705G>A (p.Trp235Ter)
dbSNP
9g.130862918G>CCA375262926ABL1c.762G>C (p.Trp254Cys)
c.705G>C (p.Trp235Cys)
9g.130862918G>TCA375262928ABL1c.762G>T (p.Trp254Cys)
c.705G>T (p.Trp235Cys)
9g.130862919G>ACA122581ABL1c.763G>A (p.Glu255Lys)
c.706G>A (p.Glu236Lys)
ClinVar dbSNP
9g.130862919G>CCA375262933ABL1c.763G>C (p.Glu255Gln)
c.706G>C (p.Glu236Gln)
9g.130862919G=CA1881463293ABL1c.763G= (p.Glu255=)
c.706G= (p.Glu236=)
9g.130862919G>TCA375262935ABL1c.763G>T (p.Glu255Ter)
c.706G>T (p.Glu236Ter)
9g.130862920A=CA1881463302ABL1c.764A= (p.Glu255=)
c.707A= (p.Glu236=)
9g.130862920A>CCA375262937ABL1c.764A>C (p.Glu255Ala)
c.707A>C (p.Glu236Ala)
9g.130862920A>GCA375262939ABL1c.764A>G (p.Glu255Gly)
c.707A>G (p.Glu236Gly)
9g.130862920A>TCA122578ABL1c.764A>T (p.Glu255Val)
c.707A>T (p.Glu236Val)
ClinVar dbSNP
9g.130862921G>ACA467496312ABL1c.765G>A (p.Glu255=)
c.708G>A (p.Glu236=)
dbSNP
9g.130862921G>CCA375262943ABL1c.765G>C (p.Glu255Asp)
c.708G>C (p.Glu236Asp)
9g.130862921G>TCA375262944ABL1c.765G>T (p.Glu255Asp)
c.708G>T (p.Glu236Asp)
9g.130862922A=CA1881463330ABL1c.766A= (p.Met256=)
c.709A= (p.Met237=)
9g.130862922A>CCA375262953ABL1c.766A>C (p.Met256Leu)
c.709A>C (p.Met237Leu)
9g.130862922A>GCA5285270ABL1c.766A>G (p.Met256Val)
c.709A>G (p.Met237Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862922A>TCA375262950ABL1c.766A>T (p.Met256Leu)
c.709A>T (p.Met237Leu)
9g.130862923T>ACA375262959ABL1c.767T>A (p.Met256Lys)
c.710T>A (p.Met237Lys)
9g.130862923T>CCA375262962ABL1c.767T>C (p.Met256Thr)
c.710T>C (p.Met237Thr)
9g.130862923T>GCA375262967ABL1c.767T>G (p.Met256Arg)
c.710T>G (p.Met237Arg)
9g.130862924G>ACA375262971ABL1c.768G>A (p.Met256Ile)
c.711G>A (p.Met237Ile)
gnomAD v4
9g.130862924G>CCA375262974ABL1c.768G>C (p.Met256Ile)
c.711G>C (p.Met237Ile)
9g.130862924G>TCA375262976ABL1c.768G>T (p.Met256Ile)
c.711G>T (p.Met237Ile)
9g.130862925G>ACA375262982ABL1c.769G>A (p.Glu257Lys)
c.712G>A (p.Glu238Lys)
COSMIC
9g.130862925G>CCA375262989ABL1c.769G>C (p.Glu257Gln)
c.712G>C (p.Glu238Gln)
9g.130862925G>TCA375262983ABL1c.769G>T (p.Glu257Ter)
c.712G>T (p.Glu238Ter)
9g.130862926A>CCA375262992ABL1c.770A>C (p.Glu257Ala)
c.713A>C (p.Glu238Ala)
9g.130862926A>GCA375262994ABL1c.770A>G (p.Glu257Gly)
c.713A>G (p.Glu238Gly)
9g.130862926A>TCA375262997ABL1c.770A>T (p.Glu257Val)
c.713A>T (p.Glu238Val)
9g.130862927A=CA1881463336ABL1c.771A= (p.Glu257=)
c.714A= (p.Glu238=)
9g.130862927A>CCA375263000ABL1c.771A>C (p.Glu257Asp)
c.714A>C (p.Glu238Asp)
9g.130862927A>GCA467496318ABL1c.771A>G (p.Glu257=)
c.714A>G (p.Glu238=)
dbSNP
9g.130862927A>TCA375263003ABL1c.771A>T (p.Glu257Asp)
c.714A>T (p.Glu238Asp)
9g.130862928C>ACA375263010ABL1c.772C>A (p.Arg258Ser)
c.715C>A (p.Arg239Ser)
9g.130862928C>GCA375263018ABL1c.772C>G (p.Arg258Gly)
c.715C>G (p.Arg239Gly)
9g.130862928C>TCA375263007ABL1c.772C>T (p.Arg258Cys)
c.715C>T (p.Arg239Cys)
ClinVar dbSNP gnomAD v4
9g.130862929G>ACA375263027ABL1c.773G>A (p.Arg258His)
c.716G>A (p.Arg239His)
ClinVar dbSNP gnomAD v2 gnomAD v4
9g.130862929G>CCA375263022ABL1c.773G>C (p.Arg258Pro)
c.716G>C (p.Arg239Pro)
9g.130862929G=CA1881463349ABL1c.773G= (p.Arg258=)
c.716G= (p.Arg239=)
9g.130862929G>TCA375263024ABL1c.773G>T (p.Arg258Leu)
c.716G>T (p.Arg239Leu)
dbSNP
9g.130862930C>ACA467496322ABL1c.774C>A (p.Arg258=)
c.717C>A (p.Arg239=)
9g.130862930C=CA1881463355ABL1c.774C= (p.Arg258=)
c.717C= (p.Arg239=)
9g.130862930C>GCA467496324ABL1c.774C>G (p.Arg258=)
c.717C>G (p.Arg239=)
9g.130862930C>TCA200680489ABL1c.774C>T (p.Arg258=)
c.717C>T (p.Arg239=)
dbSNP gnomAD v4
9g.130862931A>CCA375263035ABL1c.775A>C (p.Thr259Pro)
c.718A>C (p.Thr240Pro)
9g.130862931A>GCA375263040ABL1c.775A>G (p.Thr259Ala)
c.718A>G (p.Thr240Ala)
9g.130862931A>TCA375263043ABL1c.775A>T (p.Thr259Ser)
c.718A>T (p.Thr240Ser)
9g.130862932C>ACA375263047ABL1c.776C>A (p.Thr259Lys)
c.719C>A (p.Thr240Lys)
9g.130862932C=CA1881463363ABL1c.776C= (p.Thr259=)
c.719C= (p.Thr240=)
9g.130862932C>GCA375263049ABL1c.776C>G (p.Thr259Arg)
c.719C>G (p.Thr240Arg)
dbSNP
9g.130862932C>TCA375263051ABL1c.776C>T (p.Thr259Met)
c.719C>T (p.Thr240Met)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862933G>ACA5285271ABL1c.777G>A (p.Thr259=)
c.720G>A (p.Thr240=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862933G>CCA467496326ABL1c.777G>C (p.Thr259=)
c.720G>C (p.Thr240=)
9g.130862933G=CA1881463375ABL1c.777G= (p.Thr259=)
c.720G= (p.Thr240=)
9g.130862933G>TCA467496327ABL1c.777G>T (p.Thr259=)
c.720G>T (p.Thr240=)
9g.130862934G>ACA375263060ABL1c.778G>A (p.Asp260Asn)
c.721G>A (p.Asp241Asn)
dbSNP
9g.130862934G>CCA375263063ABL1c.778G>C (p.Asp260His)
c.721G>C (p.Asp241His)
dbSNP
9g.130862934G>TCA375263065ABL1c.778G>T (p.Asp260Tyr)
c.721G>T (p.Asp241Tyr)
9g.130862935A>CCA375263075ABL1c.779A>C (p.Asp260Ala)
c.722A>C (p.Asp241Ala)
9g.130862935A>GCA375263071ABL1c.779A>G (p.Asp260Gly)
c.722A>G (p.Asp241Gly)
9g.130862935A>TCA375263073ABL1c.779A>T (p.Asp260Val)
c.722A>T (p.Asp241Val)
9g.130862936C>ACA375263079ABL1c.780C>A (p.Asp260Glu)
c.723C>A (p.Asp241Glu)
9g.130862936C>GCA375263082ABL1c.780C>G (p.Asp260Glu)
c.723C>G (p.Asp241Glu)
9g.130862936C>TCA467496331ABL1c.780C>T (p.Asp260=)
c.723C>T (p.Asp241=)
9g.130862937A>CCA375263084ABL1c.781A>C (p.Ile261Leu)
c.724A>C (p.Ile242Leu)
9g.130862937A>GCA375263089ABL1c.781A>G (p.Ile261Val)
c.724A>G (p.Ile242Val)
9g.130862937A>TCA375263092ABL1c.781A>T (p.Ile261Phe)
c.724A>T (p.Ile242Phe)
9g.130862938T>ACA375263097ABL1c.782T>A (p.Ile261Asn)
c.725T>A (p.Ile242Asn)
9g.130862938T>CCA375263100ABL1c.782T>C (p.Ile261Thr)
c.725T>C (p.Ile242Thr)
dbSNP
9g.130862938T>GCA375263103ABL1c.782T>G (p.Ile261Ser)
c.725T>G (p.Ile242Ser)
9g.130862939C>ACA467496332ABL1c.783C>A (p.Ile261=)
c.726C>A (p.Ile242=)
9g.130862939C>GCA375263106ABL1c.783C>G (p.Ile261Met)
c.726C>G (p.Ile242Met)
COSMIC
9g.130862939C>TCA467496333ABL1c.783C>T (p.Ile261=)
c.726C>T (p.Ile242=)
dbSNP
9g.130862940A=CA1881463382ABL1c.784A= (p.Thr262=)
c.727A= (p.Thr243=)
9g.130862940A>CCA375263112ABL1c.784A>C (p.Thr262Pro)
c.727A>C (p.Thr243Pro)
9g.130862940A>GCA375263114ABL1c.784A>G (p.Thr262Ala)
c.727A>G (p.Thr243Ala)
9g.130862940A>TCA375263116ABL1c.784A>T (p.Thr262Ser)
c.727A>T (p.Thr243Ser)
dbSNP gnomAD v3 gnomAD v4
9g.130862941C>ACA375263126ABL1c.785C>A (p.Thr262Asn)
c.728C>A (p.Thr243Asn)
ClinVar dbSNP
9g.130862941C>GCA375263123ABL1c.785C>G (p.Thr262Ser)
c.728C>G (p.Thr243Ser)
9g.130862941C>TCA375263121ABL1c.785C>T (p.Thr262Ile)
c.728C>T (p.Thr243Ile)
gnomAD v4 COSMIC
9g.130862942C>ACA467496337ABL1c.786C>A (p.Thr262=)
c.729C>A (p.Thr243=)
9g.130862942C>GCA467496336ABL1c.786C>G (p.Thr262=)
c.729C>G (p.Thr243=)
9g.130862942C>TCA467496335ABL1c.786C>T (p.Thr262=)
c.729C>T (p.Thr243=)
gnomAD v4
9g.130862943A=CA1881463387ABL1c.787A= (p.Met263=)
c.730A= (p.Met244=)
9g.130862943A>CCA375263131ABL1c.787A>C (p.Met263Leu)
c.730A>C (p.Met244Leu)
gnomAD v4
9g.130862943A>GCA16602545ABL1c.787A>G (p.Met263Val)
c.730A>G (p.Met244Val)
ClinVar dbSNP COSMIC
9g.130862943A>TCA375263135ABL1c.787A>T (p.Met263Leu)
c.730A>T (p.Met244Leu)
9g.130862944T>ACA375263138ABL1c.788T>A (p.Met263Lys)
c.731T>A (p.Met244Lys)
9g.130862944T>CCA375263141ABL1c.788T>C (p.Met263Thr)
c.731T>C (p.Met244Thr)
9g.130862944T>GCA375263144ABL1c.788T>G (p.Met263Arg)
c.731T>G (p.Met244Arg)
9g.130862945G>ACA375263148ABL1c.789G>A (p.Met263Ile)
c.732G>A (p.Met244Ile)
9g.130862945G>CCA375263151ABL1c.789G>C (p.Met263Ile)
c.732G>C (p.Met244Ile)
9g.130862945G>TCA375263153ABL1c.789G>T (p.Met263Ile)
c.732G>T (p.Met244Ile)
9g.130862946A>CCA375263156ABL1c.790A>C (p.Lys264Gln)
c.733A>C (p.Lys245Gln)
9g.130862946A>GCA375263159ABL1c.790A>G (p.Lys264Glu)
c.733A>G (p.Lys245Glu)
9g.130862946A>TCA375263161ABL1c.790A>T (p.Lys264Ter)
c.733A>T (p.Lys245Ter)
9g.130862947A>CCA375263169ABL1c.791A>C (p.Lys264Thr)
c.734A>C (p.Lys245Thr)
9g.130862947A>GCA375263172ABL1c.791A>G (p.Lys264Arg)
c.734A>G (p.Lys245Arg)
9g.130862947A>TCA375263166ABL1c.791A>T (p.Lys264Met)
c.734A>T (p.Lys245Met)
gnomAD v4
9g.130862948G>ACA467496343ABL1c.792G>A (p.Lys264=)
c.735G>A (p.Lys245=)
dbSNP
9g.130862948G>CCA375263174ABL1c.792G>C (p.Lys264Asn)
c.735G>C (p.Lys245Asn)
9g.130862948G>TCA375263176ABL1c.792G>T (p.Lys264Asn)
c.735G>T (p.Lys245Asn)
9g.130862949C>ACA375263180ABL1c.793C>A (p.His265Asn)
c.736C>A (p.His246Asn)
9g.130862949C=CA1881463395ABL1c.793C= (p.His265=)
c.736C= (p.His246=)
9g.130862949C>GCA375263184ABL1c.793C>G (p.His265Asp)
c.736C>G (p.His246Asp)
dbSNP gnomAD v2 gnomAD v4
9g.130862949C>TCA375263186ABL1c.793C>T (p.His265Tyr)
c.736C>T (p.His246Tyr)
COSMIC
9g.130862950A>CCA375263196ABL1c.794A>C (p.His265Pro)
c.737A>C (p.His246Pro)
9g.130862950A>GCA375263191ABL1c.794A>G (p.His265Arg)
c.737A>G (p.His246Arg)
9g.130862950A>TCA375263195ABL1c.794A>T (p.His265Leu)
c.737A>T (p.His246Leu)
9g.130862951C>ACA375263198ABL1c.795C>A (p.His265Gln)
c.738C>A (p.His246Gln)
9g.130862951C>GCA375263199ABL1c.795C>G (p.His265Gln)
c.738C>G (p.His246Gln)
9g.130862951C>TCA467496347ABL1c.795C>T (p.His265=)
c.738C>T (p.His246=)
gnomAD v4
9g.130862952A>CCA375263202ABL1c.796A>C (p.Lys266Gln)
c.739A>C (p.Lys247Gln)
9g.130862952A>GCA375263203ABL1c.796A>G (p.Lys266Glu)
c.739A>G (p.Lys247Glu)
9g.130862952A>TCA375263205ABL1c.796A>T (p.Lys266Ter)
c.739A>T (p.Lys247Ter)
9g.130862952_130862953insGATGCAAACTCTACATGCAGGGTTTGACCCTAGGTCCTCACCTGCTGTCA2692152325ABL1c.796_797insGATGCAAACTCTACATGCAGGGTTTGACCCTAGGTCCTCACCTGCTGT (p.Lys266ArgfsTer17)
c.739_740insGATGCAAACTCTACATGCAGGGTTTGACCCTAGGTCCTCACCTGCTGT (p.Lys247ArgfsTer17)
gnomAD v4
9g.130862953A=CA1881463399ABL1c.797A= (p.Lys266=)
c.740A= (p.Lys247=)
9g.130862953A>CCA375263215ABL1c.797A>C (p.Lys266Thr)
c.740A>C (p.Lys247Thr)
9g.130862953A>GCA156560ABL1c.797A>G (p.Lys266Arg)
c.740A>G (p.Lys247Arg)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
9g.130862953A>TCA375263209ABL1c.797A>T (p.Lys266Met)
c.740A>T (p.Lys247Met)
9g.130862954G>ACA467496349ABL1c.798G>A (p.Lys266=)
c.741G>A (p.Lys247=)
9g.130862954G>CCA375263217ABL1c.798G>C (p.Lys266Asn)
c.741G>C (p.Lys247Asn)
9g.130862954G>TCA375263218ABL1c.798G>T (p.Lys266Asn)
c.741G>T (p.Lys247Asn)
9g.130862955C>ACA375263219ABL1c.799C>A (p.Leu267Met)
c.742C>A (p.Leu248Met)
dbSNP
9g.130862955C=CA1881463407ABL1c.799C= (p.Leu267=)
c.742C= (p.Leu248=)
9g.130862955C>GCA16602546ABL1c.799C>G (p.Leu267Val)
c.742C>G (p.Leu248Val)
ClinVar dbSNP COSMIC
9g.130862955C>TCA467496352ABL1c.799C>T (p.Leu267=)
c.742C>T (p.Leu248=)
9g.130862956T>ACA375263222ABL1c.800T>A (p.Leu267Gln)
c.743T>A (p.Leu248Gln)
9g.130862956T>CCA375263226ABL1c.800T>C (p.Leu267Pro)
c.743T>C (p.Leu248Pro)
9g.130862956T>GCA375263224ABL1c.800T>G (p.Leu267Arg)
c.743T>G (p.Leu248Arg)
COSMIC
9g.130862957G>ACA200680512ABL1c.801G>A (p.Leu267=)
c.744G>A (p.Leu248=)
dbSNP gnomAD v3 gnomAD v4
9g.130862957G>CCA467496354ABL1c.801G>C (p.Leu267=)
c.744G>C (p.Leu248=)
9g.130862957G=CA1881463414ABL1c.801G= (p.Leu267=)
c.744G= (p.Leu248=)
9g.130862957G>TCA467496353ABL1c.801G>T (p.Leu267=)
c.744G>T (p.Leu248=)
9g.130862958G>ACA375263229ABL1c.802G>A (p.Gly268Ser)
c.745G>A (p.Gly249Ser)
9g.130862958G>CCA375263232ABL1c.802G>C (p.Gly268Arg)
c.745G>C (p.Gly249Arg)
9g.130862958G>TCA375263231ABL1c.802G>T (p.Gly268Cys)
c.745G>T (p.Gly249Cys)
9g.130862959G>ACA375263233ABL1c.803G>A (p.Gly268Asp)
c.746G>A (p.Gly249Asp)
9g.130862959G>CCA375263237ABL1c.803G>C (p.Gly268Ala)
c.746G>C (p.Gly249Ala)
9g.130862959G>TCA375263235ABL1c.803G>T (p.Gly268Val)
c.746G>T (p.Gly249Val)
9g.130862960C>ACA467496356ABL1c.804C>A (p.Gly268=)
c.747C>A (p.Gly249=)
9g.130862960C=CA1881463417ABL1c.804C= (p.Gly268=)
c.747C= (p.Gly249=)
9g.130862960C>GCA200680517ABL1c.804C>G (p.Gly268=)
c.747C>G (p.Gly249=)
dbSNP
9g.130862960C>TCA5285272ABL1c.804C>T (p.Gly268=)
c.747C>T (p.Gly249=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862961G>ACA375263241ABL1c.805G>A (p.Gly269Arg)
c.748G>A (p.Gly250Arg)
dbSNP gnomAD v4 COSMIC COSMIC COSMIC
9g.130862961G>CCA375263244ABL1c.805G>C (p.Gly269Arg)
c.748G>C (p.Gly250Arg)
9g.130862961G=CA1881463426ABL1c.805G= (p.Gly269=)
c.748G= (p.Gly250=)
9g.130862961G>TCA375263246ABL1c.805G>T (p.Gly269Trp)
c.748G>T (p.Gly250Trp)
gnomAD v4
9g.130862965delCA2720753810ABL1c.809del (p.Gly270AlafsTer16)
c.752del (p.Gly251AlafsTer16)
dbSNP
9g.130862962G>ACA16602547ABL1c.806G>A (p.Gly269Glu)
c.749G>A (p.Gly250Glu)
ClinVar dbSNP gnomAD v4 COSMIC
9g.130862962G>CCA375263250ABL1c.806G>C (p.Gly269Ala)
c.749G>C (p.Gly250Ala)
9g.130862962G=CA1881463429ABL1c.806G= (p.Gly269=)
c.749G= (p.Gly250=)
9g.130862962G>TCA375263252ABL1c.806G>T (p.Gly269Val)
c.749G>T (p.Gly250Val)
gnomAD v4
9g.130862963G>ACA5285273ABL1c.807G>A (p.Gly269=)
c.750G>A (p.Gly250=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862963G>CCA467496357ABL1c.807G>C (p.Gly269=)
c.750G>C (p.Gly250=)
9g.130862963G=CA1881463433ABL1c.807G= (p.Gly269=)
c.750G= (p.Gly250=)
9g.130862963G>TCA467496359ABL1c.807G>T (p.Gly269=)
c.750G>T (p.Gly250=)
dbSNP gnomAD v2
9g.130862964G>ACA375263256ABL1c.808G>A (p.Gly270Ser)
c.751G>A (p.Gly251Ser)
9g.130862964G>CCA375263259ABL1c.808G>C (p.Gly270Arg)
c.751G>C (p.Gly251Arg)
9g.130862964G>TCA375263261ABL1c.808G>T (p.Gly270Cys)
c.751G>T (p.Gly251Cys)
COSMIC
9g.130862965G>ACA375263263ABL1c.809G>A (p.Gly270Asp)
c.752G>A (p.Gly251Asp)
dbSNP
9g.130862965G>CCA375263267ABL1c.809G>C (p.Gly270Ala)
c.752G>C (p.Gly251Ala)
9g.130862965G>TCA375263265ABL1c.809G>T (p.Gly270Val)
c.752G>T (p.Gly251Val)
9g.130862966C>ACA467496362ABL1c.810C>A (p.Gly270=)
c.753C>A (p.Gly251=)
9g.130862966C>GCA467496363ABL1c.810C>G (p.Gly270=)
c.753C>G (p.Gly251=)
dbSNP
9g.130862966C>TCA467496364ABL1c.810C>T (p.Gly270=)
c.753C>T (p.Gly251=)
9g.130862967C>ACA375263268ABL1c.811C>A (p.Gln271Lys)
c.754C>A (p.Gln252Lys)
9g.130862967C>GCA375263270ABL1c.811C>G (p.Gln271Glu)
c.754C>G (p.Gln252Glu)
9g.130862967C>TCA375263272ABL1c.811C>T (p.Gln271Ter)
c.754C>T (p.Gln252Ter)
9g.130862968A>CCA375263276ABL1c.812A>C (p.Gln271Pro)
c.755A>C (p.Gln252Pro)
COSMIC COSMIC COSMIC
9g.130862968A>GCA375263279ABL1c.812A>G (p.Gln271Arg)
c.755A>G (p.Gln252Arg)
gnomAD v4
9g.130862968A>TCA375263281ABL1c.812A>T (p.Gln271Leu)
c.755A>T (p.Gln252Leu)
9g.130862969G>ACA467496369ABL1c.813G>A (p.Gln271=)
c.756G>A (p.Gln252=)
dbSNP gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC
9g.130862969G>CCA16602548ABL1c.813G>C (p.Gln271His)
c.756G>C (p.Gln252His)
ClinVar dbSNP COSMIC
9g.130862969G=CA1881463456ABL1c.813G= (p.Gln271=)
c.756G= (p.Gln252=)
9g.130862969G>TCA16602549ABL1c.813G>T (p.Gln271His)
c.756G>T (p.Gln252His)
ClinVar dbSNP COSMIC
9g.130862970T>ACA375263289ABL1c.814T>A (p.Tyr272Asn)
c.757T>A (p.Tyr253Asn)
9g.130862970T>CCA122584ABL1c.814T>C (p.Tyr272His)
c.757T>C (p.Tyr253His)
ClinVar dbSNP COSMIC
9g.130862970T>GCA375263285ABL1c.814T>G (p.Tyr272Asp)
c.757T>G (p.Tyr253Asp)
9g.130862970T=CA1881463460ABL1c.814T= (p.Tyr272=)
c.757T= (p.Tyr253=)
9g.130862971A=CA1881463470ABL1c.815A= (p.Tyr272=)
c.758A= (p.Tyr253=)
9g.130862971A>CCA375263291ABL1c.815A>C (p.Tyr272Ser)
c.758A>C (p.Tyr253Ser)
9g.130862971A>GCA375263294ABL1c.815A>G (p.Tyr272Cys)
c.758A>G (p.Tyr253Cys)
dbSNP
9g.130862971A>TCA16602550ABL1c.815A>T (p.Tyr272Phe)
c.758A>T (p.Tyr253Phe)
ClinVar dbSNP COSMIC
9g.130862972C>ACA375263298ABL1c.816C>A (p.Tyr272Ter)
c.759C>A (p.Tyr253Ter)
9g.130862972C=CA1881463482ABL1c.816C= (p.Tyr272=)
c.759C= (p.Tyr253=)
9g.130862972C>GCA375263299ABL1c.816C>G (p.Tyr272Ter)
c.759C>G (p.Tyr253Ter)
dbSNP
9g.130862972C>TCA5285274ABL1c.816C>T (p.Tyr272=)
c.759C>T (p.Tyr253=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862973G>ACA375263307ABL1c.817G>A (p.Gly273Arg)
c.760G>A (p.Gly254Arg)
ClinVar dbSNP gnomAD v4
9g.130862973G>CCA375263309ABL1c.817G>C (p.Gly273Arg)
c.760G>C (p.Gly254Arg)
9g.130862973G=CA1881463488ABL1c.817G= (p.Gly273=)
c.760G= (p.Gly254=)
9g.130862973G>TCA375263311ABL1c.817G>T (p.Gly273Trp)
c.760G>T (p.Gly254Trp)
9g.130862974G>ACA375263313ABL1c.818G>A (p.Gly273Glu)
c.761G>A (p.Gly254Glu)
dbSNP
9g.130862974G>CCA375263314ABL1c.818G>C (p.Gly273Ala)
c.761G>C (p.Gly254Ala)
9g.130862974G=CA1881463500ABL1c.818G= (p.Gly273=)
c.761G= (p.Gly254=)
9g.130862974G>TCA375263315ABL1c.818G>T (p.Gly273Val)
c.761G>T (p.Gly254Val)
9g.130862975G>ACA467496376ABL1c.819G>A (p.Gly273=)
c.762G>A (p.Gly254=)
ClinVar dbSNP gnomAD v4
9g.130862975G>CCA467496378ABL1c.819G>C (p.Gly273=)
c.762G>C (p.Gly254=)
9g.130862975G=CA1881463508ABL1c.819G= (p.Gly273=)
c.762G= (p.Gly254=)
9g.130862975G>TCA467496379ABL1c.819G>T (p.Gly273=)
c.762G>T (p.Gly254=)
9g.130862976G>ACA16602551ABL1c.820G>A (p.Glu274Lys)
c.763G>A (p.Glu255Lys)
ClinVar dbSNP gnomAD v4 COSMIC
9g.130862976G>CCA375263317ABL1c.820G>C (p.Glu274Gln)
c.763G>C (p.Glu255Gln)
gnomAD v4
9g.130862976G=CA1881463513ABL1c.820G= (p.Glu274=)
c.763G= (p.Glu255=)
9g.130862976G>TCA375263320ABL1c.820G>T (p.Glu274Ter)
c.763G>T (p.Glu255Ter)
9g.130862977A=CA1881463524ABL1c.821A= (p.Glu274=)
c.764A= (p.Glu255=)
9g.130862977A>CCA375263323ABL1c.821A>C (p.Glu274Ala)
c.764A>C (p.Glu255Ala)
9g.130862977A>GCA375263326ABL1c.821A>G (p.Glu274Gly)
c.764A>G (p.Glu255Gly)
9g.130862977A>TCA16602552ABL1c.821A>T (p.Glu274Val)
c.764A>T (p.Glu255Val)
ClinVar dbSNP COSMIC

Number of alleles fetched