Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.130862763_130863035delCA645556968ABL1c.607_879del
c.550_822del
COSMIC
9g.130862776C>ACA375262304ABL1c.620C>A (p.Ser207Tyr)
c.563C>A (p.Ser188Tyr)
9g.130862776C>GCA375262305ABL1c.620C>G (p.Ser207Cys)
c.563C>G (p.Ser188Cys)
9g.130862776C>TCA375262306ABL1c.620C>T (p.Ser207Phe)
c.563C>T (p.Ser188Phe)
9g.130862777C>ACA467496171ABL1c.621C>A (p.Ser207=)
c.564C>A (p.Ser188=)
9g.130862777C=CA1881462989ABL1c.621C= (p.Ser207=)
c.564C= (p.Ser188=)
9g.130862777C>GCA467496172ABL1c.621C>G (p.Ser207=)
c.564C>G (p.Ser188=)
9g.130862777C>TCA467496173ABL1c.621C>T (p.Ser207=)
c.564C>T (p.Ser188=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862778G>ACA375262308ABL1c.622G>A (p.Glu208Lys)
c.565G>A (p.Glu189Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862778G>CCA375262310ABL1c.622G>C (p.Glu208Gln)
c.565G>C (p.Glu189Gln)
dbSNP
9g.130862778G=CA1881462996ABL1c.622G= (p.Glu208=)
c.565G= (p.Glu189=)
9g.130862778G>TCA375262312ABL1c.622G>T (p.Glu208Ter)
c.565G>T (p.Glu189Ter)
dbSNP gnomAD v3 gnomAD v4
9g.130862779A>CCA375262315ABL1c.623A>C (p.Glu208Ala)
c.566A>C (p.Glu189Ala)
9g.130862779A>GCA375262316ABL1c.623A>G (p.Glu208Gly)
c.566A>G (p.Glu189Gly)
9g.130862779A>TCA375262318ABL1c.623A>T (p.Glu208Val)
c.566A>T (p.Glu189Val)
dbSNP
9g.130862780G>ACA467496177ABL1c.624G>A (p.Glu208=)
c.567G>A (p.Glu189=)
9g.130862780G>CCA375262320ABL1c.624G>C (p.Glu208Asp)
c.567G>C (p.Glu189Asp)
9g.130862780G>TCA375262322ABL1c.624G>T (p.Glu208Asp)
c.567G>T (p.Glu189Asp)
9g.130862781A>CCA375262324ABL1c.625A>C (p.Ser209Arg)
c.568A>C (p.Ser190Arg)
9g.130862781A>GCA375262325ABL1c.625A>G (p.Ser209Gly)
c.568A>G (p.Ser190Gly)
gnomAD v4
9g.130862781A>TCA375262327ABL1c.625A>T (p.Ser209Cys)
c.568A>T (p.Ser190Cys)
dbSNP
9g.130862782G>ACA375262332ABL1c.626G>A (p.Ser209Asn)
c.569G>A (p.Ser190Asn)
dbSNP
9g.130862782G>CCA375262334ABL1c.626G>C (p.Ser209Thr)
c.569G>C (p.Ser190Thr)
dbSNP
9g.130862782G>TCA375262329ABL1c.626G>T (p.Ser209Ile)
c.569G>T (p.Ser190Ile)
dbSNP
9g.130862783C>ACA375262336ABL1c.627C>A (p.Ser209Arg)
c.570C>A (p.Ser190Arg)
ClinVar dbSNP
9g.130862783C=CA1881463000ABL1c.627C= (p.Ser209=)
c.570C= (p.Ser190=)
9g.130862783C>GCA375262338ABL1c.627C>G (p.Ser209Arg)
c.570C>G (p.Ser190Arg)
9g.130862783C>TCA467496181ABL1c.627C>T (p.Ser209=)
c.570C>T (p.Ser190=)
dbSNP
9g.130862784C>ACA375262340ABL1c.628C>A (p.Arg210Ser)
c.571C>A (p.Arg191Ser)
9g.130862784C=CA1881463002ABL1c.628C= (p.Arg210=)
c.571C= (p.Arg191=)
9g.130862784C>GCA375262342ABL1c.628C>G (p.Arg210Gly)
c.571C>G (p.Arg191Gly)
9g.130862784C>TCA5285249ABL1c.628C>T (p.Arg210Cys)
c.571C>T (p.Arg191Cys)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862785G>ACA5285250ABL1c.629G>A (p.Arg210His)
c.572G>A (p.Arg191His)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862785G>CCA375262346ABL1c.629G>C (p.Arg210Pro)
c.572G>C (p.Arg191Pro)
9g.130862785G=CA1881463008ABL1c.629G= (p.Arg210=)
c.572G= (p.Arg191=)
9g.130862785G>TCA375262347ABL1c.629G>T (p.Arg210Leu)
c.572G>T (p.Arg191Leu)
9g.130862786C>ACA467496182ABL1c.630C>A (p.Arg210=)
c.573C>A (p.Arg191=)
9g.130862786C>GCA467496184ABL1c.630C>G (p.Arg210=)
c.573C>G (p.Arg191=)
9g.130862786C>TCA467496183ABL1c.630C>T (p.Arg210=)
c.573C>T (p.Arg191=)
gnomAD v4
9g.130862787T>ACA375262350ABL1c.631T>A (p.Phe211Ile)
c.574T>A (p.Phe192Ile)
dbSNP
9g.130862787T>CCA375262352ABL1c.631T>C (p.Phe211Leu)
c.574T>C (p.Phe192Leu)
9g.130862787T>GCA375262353ABL1c.631T>G (p.Phe211Val)
c.574T>G (p.Phe192Val)
9g.130862788T>ACA375262356ABL1c.632T>A (p.Phe211Tyr)
c.575T>A (p.Phe192Tyr)
9g.130862788T>CCA375262357ABL1c.632T>C (p.Phe211Ser)
c.575T>C (p.Phe192Ser)
9g.130862788T>GCA375262359ABL1c.632T>G (p.Phe211Cys)
c.575T>G (p.Phe192Cys)
9g.130862789C>ACA375262361ABL1c.633C>A (p.Phe211Leu)
c.576C>A (p.Phe192Leu)
9g.130862789C>GCA375262362ABL1c.633C>G (p.Phe211Leu)
c.576C>G (p.Phe192Leu)
9g.130862789C>TCA467496189ABL1c.633C>T (p.Phe211=)
c.576C>T (p.Phe192=)
9g.130862790A=CA1881463013ABL1c.634A= (p.Asn212=)
c.577A= (p.Asn193=)
9g.130862790A>CCA5285251ABL1c.634A>C (p.Asn212His)
c.577A>C (p.Asn193His)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862790A>GCA375262366ABL1c.634A>G (p.Asn212Asp)
c.577A>G (p.Asn193Asp)
9g.130862790A>TCA375262367ABL1c.634A>T (p.Asn212Tyr)
c.577A>T (p.Asn193Tyr)
9g.130862791A=CA1881463016ABL1c.635A= (p.Asn212=)
c.578A= (p.Asn193=)
9g.130862791A>CCA375262370ABL1c.635A>C (p.Asn212Thr)
c.578A>C (p.Asn193Thr)
9g.130862791A>GCA5285252ABL1c.635A>G (p.Asn212Ser)
c.578A>G (p.Asn193Ser)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862791A>TCA375262373ABL1c.635A>T (p.Asn212Ile)
c.578A>T (p.Asn193Ile)
9g.130862792C>ACA375262375ABL1c.636C>A (p.Asn212Lys)
c.579C>A (p.Asn193Lys)
dbSNP gnomAD v2 gnomAD v4
9g.130862792C=CA1881463019ABL1c.636C= (p.Asn212=)
c.579C= (p.Asn193=)
9g.130862792C>GCA375262376ABL1c.636C>G (p.Asn212Lys)
c.579C>G (p.Asn193Lys)
9g.130862792C>TCA467496191ABL1c.636C>T (p.Asn212=)
c.579C>T (p.Asn193=)
dbSNP gnomAD v2 gnomAD v4
9g.130862793A=CA1881463022ABL1c.637A= (p.Thr213=)
c.580A= (p.Thr194=)
9g.130862793A>CCA375262377ABL1c.637A>C (p.Thr213Pro)
c.580A>C (p.Thr194Pro)
dbSNP
9g.130862793A>GCA375262378ABL1c.637A>G (p.Thr213Ala)
c.580A>G (p.Thr194Ala)
dbSNP gnomAD v4
9g.130862793A>TCA375262379ABL1c.637A>T (p.Thr213Ser)
c.580A>T (p.Thr194Ser)
dbSNP
9g.130862794C>ACA375262384ABL1c.638C>A (p.Thr213Asn)
c.581C>A (p.Thr194Asn)
gnomAD v4
9g.130862794C>GCA375262382ABL1c.638C>G (p.Thr213Ser)
c.581C>G (p.Thr194Ser)
9g.130862794C>TCA375262380ABL1c.638C>T (p.Thr213Ile)
c.581C>T (p.Thr194Ile)
gnomAD v4
9g.130862794_130862795insAGGACAGAGTGTTTAGAAGATCACTTCA2720751427ABL1c.638_639insAGGACAGAGTGTTTAGAAGATCACTT (p.Leu214GlyfsTer5)
c.581_582insAGGACAGAGTGTTTAGAAGATCACTT (p.Leu195GlyfsTer5)
dbSNP
9g.130862795C>ACA467496195ABL1c.639C>A (p.Thr213=)
c.582C>A (p.Thr194=)
9g.130862795C=CA1881463031ABL1c.639C= (p.Thr213=)
c.582C= (p.Thr194=)
9g.130862795C>GCA467496197ABL1c.639C>G (p.Thr213=)
c.582C>G (p.Thr194=)
ClinVar dbSNP gnomAD v2 gnomAD v4
9g.130862795C>TCA467496199ABL1c.639C>T (p.Thr213=)
c.582C>T (p.Thr194=)
9g.130862796C>ACA375262385ABL1c.640C>A (p.Leu214Met)
c.583C>A (p.Leu195Met)
9g.130862796C=CA1881463037ABL1c.640C= (p.Leu214=)
c.583C= (p.Leu195=)
9g.130862796C>GCA375262387ABL1c.640C>G (p.Leu214Val)
c.583C>G (p.Leu195Val)
dbSNP gnomAD v2 gnomAD v4
9g.130862796C>TCA467496200ABL1c.640C>T (p.Leu214=)
c.583C>T (p.Leu195=)
gnomAD v4
9g.130862797T>ACA375262390ABL1c.641T>A (p.Leu214Gln)
c.584T>A (p.Leu195Gln)
dbSNP
9g.130862797T>CCA375262393ABL1c.641T>C (p.Leu214Pro)
c.584T>C (p.Leu195Pro)
9g.130862797T>GCA375262391ABL1c.641T>G (p.Leu214Arg)
c.584T>G (p.Leu195Arg)
9g.130862798G>ACA467496205ABL1c.642G>A (p.Leu214=)
c.585G>A (p.Leu195=)
dbSNP
9g.130862798G>CCA467496207ABL1c.642G>C (p.Leu214=)
c.585G>C (p.Leu195=)
9g.130862798G=CA1881463041ABL1c.642G= (p.Leu214=)
c.585G= (p.Leu195=)
9g.130862798G>TCA467496208ABL1c.642G>T (p.Leu214=)
c.585G>T (p.Leu195=)
9g.130862799G>ACA375262395ABL1c.643G>A (p.Ala215Thr)
c.586G>A (p.Ala196Thr)
dbSNP
9g.130862799G>CCA5285253ABL1c.643G>C (p.Ala215Pro)
c.586G>C (p.Ala196Pro)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862799G=CA1881463044ABL1c.643G= (p.Ala215=)
c.586G= (p.Ala196=)
9g.130862799G>TCA375262398ABL1c.643G>T (p.Ala215Ser)
c.586G>T (p.Ala196Ser)
9g.130862800C>ACA375262400ABL1c.644C>A (p.Ala215Asp)
c.587C>A (p.Ala196Asp)
9g.130862800C>GCA375262402ABL1c.644C>G (p.Ala215Gly)
c.587C>G (p.Ala196Gly)
9g.130862800C>TCA375262404ABL1c.644C>T (p.Ala215Val)
c.587C>T (p.Ala196Val)
9g.130862801C>ACA467496216ABL1c.645C>A (p.Ala215=)
c.588C>A (p.Ala196=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862801C=CA1881463049ABL1c.645C= (p.Ala215=)
c.588C= (p.Ala196=)
9g.130862801C>GCA5285255ABL1c.645C>G (p.Ala215=)
c.588C>G (p.Ala196=)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862801C>TCA5285254ABL1c.645C>T (p.Ala215=)
c.588C>T (p.Ala196=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862802G>ACA5285256ABL1c.646G>A (p.Glu216Lys)
c.589G>A (p.Glu197Lys)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862802G>CCA375262409ABL1c.646G>C (p.Glu216Gln)
c.589G>C (p.Glu197Gln)
dbSNP gnomAD v4
9g.130862802G=CA1881463058ABL1c.646G= (p.Glu216=)
c.589G= (p.Glu197=)
9g.130862802G>TCA375262411ABL1c.646G>T (p.Glu216Ter)
c.589G>T (p.Glu197Ter)
9g.130862803A=CA1881463065ABL1c.647A= (p.Glu216=)
c.590A= (p.Glu197=)
9g.130862803A>CCA375262415ABL1c.647A>C (p.Glu216Ala)
c.590A>C (p.Glu197Ala)
9g.130862803A>GCA5285257ABL1c.647A>G (p.Glu216Gly)
c.590A>G (p.Glu197Gly)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862803A>TCA375262413ABL1c.647A>T (p.Glu216Val)
c.590A>T (p.Glu197Val)
9g.130862804G>ACA467496223ABL1c.648G>A (p.Glu216=)
c.591G>A (p.Glu197=)
dbSNP gnomAD v2 gnomAD v4
9g.130862804G>CCA375262417ABL1c.648G>C (p.Glu216Asp)
c.591G>C (p.Glu197Asp)
9g.130862804G=CA1881463073ABL1c.648G= (p.Glu216=)
c.591G= (p.Glu197=)
9g.130862804G>TCA375262420ABL1c.648G>T (p.Glu216Asp)
c.591G>T (p.Glu197Asp)
9g.130862805T>ACA375262422ABL1c.649T>A (p.Leu217Met)
c.592T>A (p.Leu198Met)
9g.130862805T>CCA5285259ABL1c.649T>C (p.Leu217=)
c.592T>C (p.Leu198=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862805T>GCA5285258ABL1c.649T>G (p.Leu217Val)
c.592T>G (p.Leu198Val)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862805T=CA1881463081ABL1c.649T= (p.Leu217=)
c.592T= (p.Leu198=)
9g.130862806T>ACA375262425ABL1c.650T>A (p.Leu217Ter)
c.593T>A (p.Leu198Ter)
9g.130862806T>CCA375262427ABL1c.650T>C (p.Leu217Ser)
c.593T>C (p.Leu198Ser)
9g.130862806T>GCA375262429ABL1c.650T>G (p.Leu217Trp)
c.593T>G (p.Leu198Trp)
9g.130862807G>ACA467496232ABL1c.651G>A (p.Leu217=)
c.594G>A (p.Leu198=)
9g.130862807G>CCA375262431ABL1c.651G>C (p.Leu217Phe)
c.594G>C (p.Leu198Phe)
dbSNP
9g.130862807G=CA1881463087ABL1c.651G= (p.Leu217=)
c.594G= (p.Leu198=)
9g.130862807G>TCA375262433ABL1c.651G>T (p.Leu217Phe)
c.594G>T (p.Leu198Phe)
9g.130862808G>ACA375262437ABL1c.652G>A (p.Val218Ile)
c.595G>A (p.Val199Ile)
ClinVar dbSNP
9g.130862808G>CCA375262438ABL1c.652G>C (p.Val218Leu)
c.595G>C (p.Val199Leu)
9g.130862808G=CA1881463091ABL1c.652G= (p.Val218=)
c.595G= (p.Val199=)
9g.130862808G>TCA375262436ABL1c.652G>T (p.Val218Phe)
c.595G>T (p.Val199Phe)
9g.130862809T>ACA375262441ABL1c.653T>A (p.Val218Asp)
c.596T>A (p.Val199Asp)
9g.130862809T>CCA375262442ABL1c.653T>C (p.Val218Ala)
c.596T>C (p.Val199Ala)
9g.130862809T>GCA375262444ABL1c.653T>G (p.Val218Gly)
c.596T>G (p.Val199Gly)
dbSNP
9g.130862810T>ACA467496240ABL1c.654T>A (p.Val218=)
c.597T>A (p.Val199=)
9g.130862810T>CCA467496238ABL1c.654T>C (p.Val218=)
c.597T>C (p.Val199=)
9g.130862810T>GCA200680459ABL1c.654T>G (p.Val218=)
c.597T>G (p.Val199=)
ClinVar dbSNP
9g.130862810T=CA1881463097ABL1c.654T= (p.Val218=)
c.597T= (p.Val199=)
9g.130862811C>ACA375262447ABL1c.655C>A (p.His219Asn)
c.598C>A (p.His200Asn)
9g.130862811C>GCA375262448ABL1c.655C>G (p.His219Asp)
c.598C>G (p.His200Asp)
9g.130862811C>TCA375262450ABL1c.655C>T (p.His219Tyr)
c.598C>T (p.His200Tyr)
9g.130862812A>CCA375262456ABL1c.656A>C (p.His219Pro)
c.599A>C (p.His200Pro)
9g.130862812A>GCA375262452ABL1c.656A>G (p.His219Arg)
c.599A>G (p.His200Arg)
9g.130862812A>TCA375262454ABL1c.656A>T (p.His219Leu)
c.599A>T (p.His200Leu)
9g.130862813T>ACA375262458ABL1c.657T>A (p.His219Gln)
c.600T>A (p.His200Gln)
9g.130862813T>CCA467496250ABL1c.657T>C (p.His219=)
c.600T>C (p.His200=)
gnomAD v4
9g.130862813T>GCA375262459ABL1c.657T>G (p.His219Gln)
c.600T>G (p.His200Gln)
9g.130862814C>ACA375262460ABL1c.658C>A (p.His220Asn)
c.601C>A (p.His201Asn)
9g.130862814C>GCA375262461ABL1c.658C>G (p.His220Asp)
c.601C>G (p.His201Asp)
9g.130862814C>TCA375262462ABL1c.658C>T (p.His220Tyr)
c.601C>T (p.His201Tyr)
COSMIC COSMIC COSMIC
9g.130862815A>CCA375262463ABL1c.659A>C (p.His220Pro)
c.602A>C (p.His201Pro)
9g.130862815A>GCA375262465ABL1c.659A>G (p.His220Arg)
c.602A>G (p.His201Arg)
9g.130862815A>TCA375262464ABL1c.659A>T (p.His220Leu)
c.602A>T (p.His201Leu)
9g.130862816T>ACA375262466ABL1c.660T>A (p.His220Gln)
c.603T>A (p.His201Gln)
9g.130862816T>CCA467496257ABL1c.660T>C (p.His220=)
c.603T>C (p.His201=)
9g.130862816T>GCA375262468ABL1c.660T>G (p.His220Gln)
c.603T>G (p.His201Gln)
9g.130862817C>ACA375262469ABL1c.661C>A (p.His221Asn)
c.604C>A (p.His202Asn)
9g.130862817C>GCA375262470ABL1c.661C>G (p.His221Asp)
c.604C>G (p.His202Asp)
dbSNP
9g.130862817C>TCA375262471ABL1c.661C>T (p.His221Tyr)
c.604C>T (p.His202Tyr)
9g.130862818A>CCA375262472ABL1c.662A>C (p.His221Pro)
c.605A>C (p.His202Pro)
9g.130862818A>GCA375262473ABL1c.662A>G (p.His221Arg)
c.605A>G (p.His202Arg)
9g.130862818A>TCA375262474ABL1c.662A>T (p.His221Leu)
c.605A>T (p.His202Leu)
9g.130862819T>ACA375262475ABL1c.663T>A (p.His221Gln)
c.606T>A (p.His202Gln)
9g.130862819T>CCA5285260ABL1c.663T>C (p.His221=)
c.606T>C (p.His202=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862819T>GCA375262476ABL1c.663T>G (p.His221Gln)
c.606T>G (p.His202Gln)
9g.130862819T=CA1881463104ABL1c.663T= (p.His221=)
c.606T= (p.His202=)
9g.130862820T>ACA375262479ABL1c.664T>A (p.Ser222Thr)
c.607T>A (p.Ser203Thr)
9g.130862820T>CCA375262478ABL1c.664T>C (p.Ser222Pro)
c.607T>C (p.Ser203Pro)
9g.130862820T>GCA375262477ABL1c.664T>G (p.Ser222Ala)
c.607T>G (p.Ser203Ala)
9g.130862821C>ACA375262480ABL1c.665C>A (p.Ser222Ter)
c.608C>A (p.Ser203Ter)
gnomAD v4
9g.130862821C=CA1881463111ABL1c.665C= (p.Ser222=)
c.608C= (p.Ser203=)
9g.130862821C>GCA375262482ABL1c.665C>G (p.Ser222Ter)
c.608C>G (p.Ser203Ter)
9g.130862821C>TCA375262481ABL1c.665C>T (p.Ser222Leu)
c.608C>T (p.Ser203Leu)
dbSNP
9g.130862822A>CCA467496267ABL1c.666A>C (p.Ser222=)
c.609A>C (p.Ser203=)
9g.130862822A>GCA467496268ABL1c.666A>G (p.Ser222=)
c.609A>G (p.Ser203=)
9g.130862822A>TCA467496270ABL1c.666A>T (p.Ser222=)
c.609A>T (p.Ser203=)
9g.130862823A=CA1881463113ABL1c.667A= (p.Thr223=)
c.610A= (p.Thr204=)
9g.130862823A>CCA375262483ABL1c.667A>C (p.Thr223Pro)
c.610A>C (p.Thr204Pro)
9g.130862823A>GCA375262484ABL1c.667A>G (p.Thr223Ala)
c.610A>G (p.Thr204Ala)
ClinVar dbSNP gnomAD v2 gnomAD v4
9g.130862823A>TCA375262485ABL1c.667A>T (p.Thr223Ser)
c.610A>T (p.Thr204Ser)
9g.130862824C>ACA375262486ABL1c.668C>A (p.Thr223Lys)
c.611C>A (p.Thr204Lys)
9g.130862824C=CA1881463117ABL1c.668C= (p.Thr223=)
c.611C= (p.Thr204=)
9g.130862824C>GCA375262487ABL1c.668C>G (p.Thr223Arg)
c.611C>G (p.Thr204Arg)
dbSNP
9g.130862824C>TCA5285261ABL1c.668C>T (p.Thr223Met)
c.611C>T (p.Thr204Met)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862825G>ACA467496273ABL1c.669G>A (p.Thr223=)
c.612G>A (p.Thr204=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862825G>CCA467496275ABL1c.669G>C (p.Thr223=)
c.612G>C (p.Thr204=)
gnomAD v4 COSMIC COSMIC COSMIC
9g.130862825G=CA1881463122ABL1c.669G= (p.Thr223=)
c.612G= (p.Thr204=)
9g.130862825G>TCA467496277ABL1c.669G>T (p.Thr223=)
c.612G>T (p.Thr204=)
dbSNP
9g.130862826G>ACA375262488ABL1c.670G>A (p.Val224Met)
c.613G>A (p.Val205Met)
dbSNP
9g.130862826G>CCA375262489ABL1c.670G>C (p.Val224Leu)
c.613G>C (p.Val205Leu)
dbSNP
9g.130862826G=CA1881463127ABL1c.670G= (p.Val224=)
c.613G= (p.Val205=)
9g.130862826G>TCA375262490ABL1c.670G>T (p.Val224Leu)
c.613G>T (p.Val205Leu)
9g.130862827T>ACA375262491ABL1c.671T>A (p.Val224Glu)
c.614T>A (p.Val205Glu)
9g.130862827T>CCA375262492ABL1c.671T>C (p.Val224Ala)
c.614T>C (p.Val205Ala)
9g.130862827T>GCA375262493ABL1c.671T>G (p.Val224Gly)
c.614T>G (p.Val205Gly)
9g.130862828G>ACA467496282ABL1c.672G>A (p.Val224=)
c.615G>A (p.Val205=)
ClinVar gnomAD v4
9g.130862828G>CCA467496283ABL1c.672G>C (p.Val224=)
c.615G>C (p.Val205=)
dbSNP
9g.130862828G=CA1881463130ABL1c.672G= (p.Val224=)
c.615G= (p.Val205=)
9g.130862828G>TCA467496284ABL1c.672G>T (p.Val224=)
c.615G>T (p.Val205=)
9g.130862829G>ACA375262494ABL1c.673G>A (p.Ala225Thr)
c.616G>A (p.Ala206Thr)
dbSNP gnomAD v2 gnomAD v4
9g.130862829G>CCA375262496ABL1c.673G>C (p.Ala225Pro)
c.616G>C (p.Ala206Pro)
dbSNP
9g.130862829G=CA1881463139ABL1c.673G= (p.Ala225=)
c.616G= (p.Ala206=)
9g.130862829G>TCA375262495ABL1c.673G>T (p.Ala225Ser)
c.616G>T (p.Ala206Ser)
dbSNP
9g.130862830C>ACA375262497ABL1c.674C>A (p.Ala225Asp)
c.617C>A (p.Ala206Asp)
dbSNP
9g.130862830C>GCA375262498ABL1c.674C>G (p.Ala225Gly)
c.617C>G (p.Ala206Gly)
dbSNP
9g.130862830C>TCA375262499ABL1c.674C>T (p.Ala225Val)
c.617C>T (p.Ala206Val)
dbSNP COSMIC COSMIC COSMIC
9g.130862831C>ACA467496293ABL1c.675C>A (p.Ala225=)
c.618C>A (p.Ala206=)
dbSNP
9g.130862831C=CA1881463144ABL1c.675C= (p.Ala225=)
c.618C= (p.Ala206=)
9g.130862831C>GCA467496295ABL1c.675C>G (p.Ala225=)
c.618C>G (p.Ala206=)
gnomAD v4
9g.130862831C>TCA5285262ABL1c.675C>T (p.Ala225=)
c.618C>T (p.Ala206=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862832G>ACA375262500ABL1c.676G>A (p.Asp226Asn)
c.619G>A (p.Asp207Asn)
ClinVar dbSNP gnomAD v4
9g.130862832G>CCA375262501ABL1c.676G>C (p.Asp226His)
c.619G>C (p.Asp207His)
9g.130862832G=CA1881463153ABL1c.676G= (p.Asp226=)
c.619G= (p.Asp207=)
9g.130862832G>TCA375262502ABL1c.676G>T (p.Asp226Tyr)
c.619G>T (p.Asp207Tyr)
9g.130862833A>CCA375262503ABL1c.677A>C (p.Asp226Ala)
c.620A>C (p.Asp207Ala)
dbSNP
9g.130862833A>GCA375262504ABL1c.677A>G (p.Asp226Gly)
c.620A>G (p.Asp207Gly)
9g.130862833A>TCA375262505ABL1c.677A>T (p.Asp226Val)
c.620A>T (p.Asp207Val)
9g.130862834C>ACA375262506ABL1c.678C>A (p.Asp226Glu)
c.621C>A (p.Asp207Glu)
gnomAD v4 COSMIC
9g.130862834C=CA1881463158ABL1c.678C= (p.Asp226=)
c.621C= (p.Asp207=)
9g.130862834C>GCA375262507ABL1c.678C>G (p.Asp226Glu)
c.621C>G (p.Asp207Glu)
dbSNP
9g.130862834C>TCA5285263ABL1c.678C>T (p.Asp226=)
c.621C>T (p.Asp207=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862835G>ACA375262508ABL1c.679G>A (p.Gly227Arg)
c.622G>A (p.Gly208Arg)
dbSNP gnomAD v4
9g.130862835G>CCA375262509ABL1c.679G>C (p.Gly227Arg)
c.622G>C (p.Gly208Arg)
9g.130862835G>TCA375262510ABL1c.679G>T (p.Gly227Trp)
c.622G>T (p.Gly208Trp)
9g.130862836G>ACA375262511ABL1c.680G>A (p.Gly227Glu)
c.623G>A (p.Gly208Glu)
9g.130862836G>CCA375262512ABL1c.680G>C (p.Gly227Ala)
c.623G>C (p.Gly208Ala)
dbSNP
9g.130862836G>TCA375262513ABL1c.680G>T (p.Gly227Val)
c.623G>T (p.Gly208Val)
9g.130862837G>ACA467496194ABL1c.681G>A (p.Gly227=)
c.624G>A (p.Gly208=)
dbSNP gnomAD v4
9g.130862837G>CCA467496196ABL1c.681G>C (p.Gly227=)
c.624G>C (p.Gly208=)
9g.130862837G>TCA467496198ABL1c.681G>T (p.Gly227=)
c.624G>T (p.Gly208=)
9g.130862838C>ACA375262514ABL1c.682C>A (p.Leu228Ile)
c.625C>A (p.Leu209Ile)
dbSNP
9g.130862838C>GCA375262515ABL1c.682C>G (p.Leu228Val)
c.625C>G (p.Leu209Val)
9g.130862838C>TCA375262516ABL1c.682C>T (p.Leu228Phe)
c.625C>T (p.Leu209Phe)
dbSNP
9g.130862839T>ACA375262517ABL1c.683T>A (p.Leu228His)
c.626T>A (p.Leu209His)
9g.130862839T>CCA375262518ABL1c.683T>C (p.Leu228Pro)
c.626T>C (p.Leu209Pro)
9g.130862839T>GCA375262519ABL1c.683T>G (p.Leu228Arg)
c.626T>G (p.Leu209Arg)
9g.130862840C>ACA467496201ABL1c.684C>A (p.Leu228=)
c.627C>A (p.Leu209=)
9g.130862840C>GCA467496204ABL1c.684C>G (p.Leu228=)
c.627C>G (p.Leu209=)
gnomAD v4
9g.130862840C>TCA467496202ABL1c.684C>T (p.Leu228=)
c.627C>T (p.Leu209=)
9g.130862841A=CA1881463160ABL1c.685A= (p.Ile229=)
c.628A= (p.Ile210=)
9g.130862841A>CCA375262521ABL1c.685A>C (p.Ile229Leu)
c.628A>C (p.Ile210Leu)
9g.130862841A>GCA375262522ABL1c.685A>G (p.Ile229Val)
c.628A>G (p.Ile210Val)
dbSNP gnomAD v4
9g.130862841A>TCA375262520ABL1c.685A>T (p.Ile229Phe)
c.628A>T (p.Ile210Phe)
9g.130862842T>ACA375262523ABL1c.686T>A (p.Ile229Asn)
c.629T>A (p.Ile210Asn)
9g.130862842T>CCA375262524ABL1c.686T>C (p.Ile229Thr)
c.629T>C (p.Ile210Thr)
9g.130862842T>GCA375262525ABL1c.686T>G (p.Ile229Ser)
c.629T>G (p.Ile210Ser)
9g.130862843C>ACA467496206ABL1c.687C>A (p.Ile229=)
c.630C>A (p.Ile210=)
9g.130862843C=CA1881463161ABL1c.687C= (p.Ile229=)
c.630C= (p.Ile210=)
9g.130862843C>GCA375262526ABL1c.687C>G (p.Ile229Met)
c.630C>G (p.Ile210Met)
9g.130862843C>TCA5285264ABL1c.687C>T (p.Ile229=)
c.630C>T (p.Ile210=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862844A>CCA375262533ABL1c.688A>C (p.Thr230Pro)
c.631A>C (p.Thr211Pro)
9g.130862844A>GCA375262528ABL1c.688A>G (p.Thr230Ala)
c.631A>G (p.Thr211Ala)
9g.130862844A>TCA375262530ABL1c.688A>T (p.Thr230Ser)
c.631A>T (p.Thr211Ser)
9g.130862845C>ACA375262536ABL1c.689C>A (p.Thr230Asn)
c.632C>A (p.Thr211Asn)
9g.130862845C>GCA375262538ABL1c.689C>G (p.Thr230Ser)
c.632C>G (p.Thr211Ser)
dbSNP
9g.130862845C>TCA375262540ABL1c.689C>T (p.Thr230Ile)
c.632C>T (p.Thr211Ile)
gnomAD v4
9g.130862846C>ACA467496210ABL1c.690C>A (p.Thr230=)
c.633C>A (p.Thr211=)
9g.130862846C>GCA467496211ABL1c.690C>G (p.Thr230=)
c.633C>G (p.Thr211=)
9g.130862846C>TCA467496212ABL1c.690C>T (p.Thr230=)
c.633C>T (p.Thr211=)
gnomAD v4
9g.130862847A>CCA375262543ABL1c.691A>C (p.Thr231Pro)
c.634A>C (p.Thr212Pro)
9g.130862847A>GCA375262545ABL1c.691A>G (p.Thr231Ala)
c.634A>G (p.Thr212Ala)
9g.130862847A>TCA375262547ABL1c.691A>T (p.Thr231Ser)
c.634A>T (p.Thr212Ser)
9g.130862848C>ACA375262551ABL1c.692C>A (p.Thr231Lys)
c.635C>A (p.Thr212Lys)
9g.130862848C=CA1881463164ABL1c.692C= (p.Thr231=)
c.635C= (p.Thr212=)
9g.130862848C>GCA375262553ABL1c.692C>G (p.Thr231Arg)
c.635C>G (p.Thr212Arg)
9g.130862848C>TCA200680473ABL1c.692C>T (p.Thr231Met)
c.635C>T (p.Thr212Met)
ClinVar dbSNP gnomAD v3 gnomAD v4
9g.130862849G>ACA5285265ABL1c.693G>A (p.Thr231=)
c.636G>A (p.Thr212=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862849G>CCA467496214ABL1c.693G>C (p.Thr231=)
c.636G>C (p.Thr212=)
dbSNP
9g.130862849G=CA1881463170ABL1c.693G= (p.Thr231=)
c.636G= (p.Thr212=)
9g.130862849G>TCA467496215ABL1c.693G>T (p.Thr231=)
c.636G>T (p.Thr212=)
9g.130862850C>ACA375262557ABL1c.694C>A (p.Leu232Ile)
c.637C>A (p.Leu213Ile)
gnomAD v4
9g.130862850C>GCA375262558ABL1c.694C>G (p.Leu232Val)
c.637C>G (p.Leu213Val)
9g.130862850C>TCA375262561ABL1c.694C>T (p.Leu232Phe)
c.637C>T (p.Leu213Phe)
9g.130862851T>ACA375262563ABL1c.695T>A (p.Leu232His)
c.638T>A (p.Leu213His)
9g.130862851T>CCA375262565ABL1c.695T>C (p.Leu232Pro)
c.638T>C (p.Leu213Pro)
9g.130862851T>GCA375262567ABL1c.695T>G (p.Leu232Arg)
c.638T>G (p.Leu213Arg)
9g.130862852C>ACA467496217ABL1c.696C>A (p.Leu232=)
c.639C>A (p.Leu213=)
9g.130862852C>GCA467496218ABL1c.696C>G (p.Leu232=)
c.639C>G (p.Leu213=)
9g.130862852C>TCA467496219ABL1c.696C>T (p.Leu232=)
c.639C>T (p.Leu213=)
gnomAD v4
9g.130862853C>ACA375262574ABL1c.697C>A (p.His233Asn)
c.640C>A (p.His214Asn)
9g.130862853C>GCA375262570ABL1c.697C>G (p.His233Asp)
c.640C>G (p.His214Asp)
9g.130862853C>TCA375262572ABL1c.697C>T (p.His233Tyr)
c.640C>T (p.His214Tyr)
9g.130862854A>CCA375262577ABL1c.698A>C (p.His233Pro)
c.641A>C (p.His214Pro)
9g.130862854A>GCA375262579ABL1c.698A>G (p.His233Arg)
c.641A>G (p.His214Arg)
9g.130862854A>TCA375262581ABL1c.698A>T (p.His233Leu)
c.641A>T (p.His214Leu)
9g.130862855T>ACA375262583ABL1c.699T>A (p.His233Gln)
c.642T>A (p.His214Gln)
9g.130862855T>CCA467496221ABL1c.699T>C (p.His233=)
c.642T>C (p.His214=)
9g.130862855T>GCA375262585ABL1c.699T>G (p.His233Gln)
c.642T>G (p.His214Gln)
9g.130862856T>ACA375262586ABL1c.700T>A (p.Tyr234Asn)
c.643T>A (p.Tyr215Asn)
9g.130862856T>CCA375262591ABL1c.700T>C (p.Tyr234His)
c.643T>C (p.Tyr215His)
9g.130862856T>GCA375262589ABL1c.700T>G (p.Tyr234Asp)
c.643T>G (p.Tyr215Asp)
9g.130862857A=CA1881463176ABL1c.701A= (p.Tyr234=)
c.644A= (p.Tyr215=)
9g.130862857A>CCA375262594ABL1c.701A>C (p.Tyr234Ser)
c.644A>C (p.Tyr215Ser)
9g.130862857A>GCA375262596ABL1c.701A>G (p.Tyr234Cys)
c.644A>G (p.Tyr215Cys)
9g.130862857A>TCA375262598ABL1c.701A>T (p.Tyr234Phe)
c.644A>T (p.Tyr215Phe)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
9g.130862858T>ACA375262599ABL1c.702T>A (p.Tyr234Ter)
c.645T>A (p.Tyr215Ter)
9g.130862858T>CCA467496224ABL1c.702T>C (p.Tyr234=)
c.645T>C (p.Tyr215=)
9g.130862858T>GCA375262601ABL1c.702T>G (p.Tyr234Ter)
c.645T>G (p.Tyr215Ter)
9g.130862859C>ACA375262604ABL1c.703C>A (p.Pro235Thr)
c.646C>A (p.Pro216Thr)
9g.130862859C>GCA375262606ABL1c.703C>G (p.Pro235Ala)
c.646C>G (p.Pro216Ala)
dbSNP
9g.130862859C>TCA375262608ABL1c.703C>T (p.Pro235Ser)
c.646C>T (p.Pro216Ser)
9g.130862860C>ACA375262611ABL1c.704C>A (p.Pro235Gln)
c.647C>A (p.Pro216Gln)
9g.130862860C>GCA375262613ABL1c.704C>G (p.Pro235Arg)
c.647C>G (p.Pro216Arg)
9g.130862860C>TCA375262615ABL1c.704C>T (p.Pro235Leu)
c.647C>T (p.Pro216Leu)
9g.130862861A>CCA467496228ABL1c.705A>C (p.Pro235=)
c.648A>C (p.Pro216=)
9g.130862861A>GCA467496229ABL1c.705A>G (p.Pro235=)
c.648A>G (p.Pro216=)
gnomAD v4
9g.130862861A>TCA467496227ABL1c.705A>T (p.Pro235=)
c.648A>T (p.Pro216=)
9g.130862862G>ACA375262622ABL1c.706G>A (p.Ala236Thr)
c.649G>A (p.Ala217Thr)
dbSNP gnomAD v4
9g.130862862G>CCA375262620ABL1c.706G>C (p.Ala236Pro)
c.649G>C (p.Ala217Pro)
9g.130862862G>TCA375262618ABL1c.706G>T (p.Ala236Ser)
c.649G>T (p.Ala217Ser)
9g.130862863C>ACA375262629ABL1c.707C>A (p.Ala236Asp)
c.650C>A (p.Ala217Asp)
9g.130862863C>GCA375262625ABL1c.707C>G (p.Ala236Gly)
c.650C>G (p.Ala217Gly)
9g.130862863C>TCA375262627ABL1c.707C>T (p.Ala236Val)
c.650C>T (p.Ala217Val)
dbSNP
9g.130862864C>ACA467496235ABL1c.708C>A (p.Ala236=)
c.651C>A (p.Ala217=)
dbSNP
9g.130862864C>GCA467496234ABL1c.708C>G (p.Ala236=)
c.651C>G (p.Ala217=)
gnomAD v4
9g.130862864C>TCA467496233ABL1c.708C>T (p.Ala236=)
c.651C>T (p.Ala217=)
gnomAD v4
9g.130862865C>ACA375262632ABL1c.709C>A (p.Pro237Thr)
c.652C>A (p.Pro218Thr)
9g.130862865C>GCA375262634ABL1c.709C>G (p.Pro237Ala)
c.652C>G (p.Pro218Ala)
9g.130862865C>TCA375262635ABL1c.709C>T (p.Pro237Ser)
c.652C>T (p.Pro218Ser)
COSMIC COSMIC COSMIC
9g.130862866C>ACA375262639ABL1c.710C>A (p.Pro237Gln)
c.653C>A (p.Pro218Gln)
9g.130862866C>GCA375262641ABL1c.710C>G (p.Pro237Arg)
c.653C>G (p.Pro218Arg)
9g.130862866C>TCA375262642ABL1c.710C>T (p.Pro237Leu)
c.653C>T (p.Pro218Leu)
9g.130862867A>CCA467496239ABL1c.711A>C (p.Pro237=)
c.654A>C (p.Pro218=)
9g.130862867A>GCA467496243ABL1c.711A>G (p.Pro237=)
c.654A>G (p.Pro218=)
9g.130862867A>TCA467496241ABL1c.711A>T (p.Pro237=)
c.654A>T (p.Pro218=)
9g.130862868A>CCA375262645ABL1c.712A>C (p.Lys238Gln)
c.655A>C (p.Lys219Gln)
9g.130862868A>GCA375262646ABL1c.712A>G (p.Lys238Glu)
c.655A>G (p.Lys219Glu)
9g.130862868A>TCA375262649ABL1c.712A>T (p.Lys238Ter)
c.655A>T (p.Lys219Ter)
9g.130862869A>CCA375262651ABL1c.713A>C (p.Lys238Thr)
c.656A>C (p.Lys219Thr)
9g.130862869A>GCA375262653ABL1c.713A>G (p.Lys238Arg)
c.656A>G (p.Lys219Arg)
9g.130862869A>TCA375262655ABL1c.713A>T (p.Lys238Met)
c.656A>T (p.Lys219Met)
9g.130862870G>ACA467496246ABL1c.714G>A (p.Lys238=)
c.657G>A (p.Lys219=)
gnomAD v4
9g.130862870G>CCA375262661ABL1c.714G>C (p.Lys238Asn)
c.657G>C (p.Lys219Asn)
9g.130862870G>TCA375262659ABL1c.714G>T (p.Lys238Asn)
c.657G>T (p.Lys219Asn)
9g.130862871C>ACA375262664ABL1c.715C>A (p.Arg239Ser)
c.658C>A (p.Arg220Ser)
dbSNP gnomAD v3 gnomAD v4
9g.130862871C=CA1881463179ABL1c.715C= (p.Arg239=)
c.658C= (p.Arg220=)
9g.130862871C>GCA375262666ABL1c.715C>G (p.Arg239Gly)
c.658C>G (p.Arg220Gly)
9g.130862871C>TCA5285266ABL1c.715C>T (p.Arg239Cys)
c.658C>T (p.Arg220Cys)
dbSNP ExAC gnomAD v2 gnomAD v4
9g.130862872G>ACA375262671ABL1c.716G>A (p.Arg239His)
c.659G>A (p.Arg220His)
ClinVar dbSNP gnomAD v4
9g.130862872G>CCA375262672ABL1c.716G>C (p.Arg239Pro)
c.659G>C (p.Arg220Pro)
dbSNP
9g.130862872G=CA1881463187ABL1c.716G= (p.Arg239=)
c.659G= (p.Arg220=)
9g.130862872G>TCA5285267ABL1c.716G>T (p.Arg239Leu)
c.659G>T (p.Arg220Leu)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
9g.130862873C>ACA467496251ABL1c.717C>A (p.Arg239=)
c.660C>A (p.Arg220=)
9g.130862873C>GCA467496252ABL1c.717C>G (p.Arg239=)
c.660C>G (p.Arg220=)
9g.130862873C>TCA467496255ABL1c.717C>T (p.Arg239=)
c.660C>T (p.Arg220=)
9g.130862874A>CCA375262675ABL1c.718A>C (p.Asn240His)
c.661A>C (p.Asn221His)
9g.130862874A>GCA375262677ABL1c.718A>G (p.Asn240Asp)
c.661A>G (p.Asn221Asp)
9g.130862874A>TCA375262679ABL1c.718A>T (p.Asn240Tyr)
c.661A>T (p.Asn221Tyr)
9g.130862875A>CCA375262683ABL1c.719A>C (p.Asn240Thr)
c.662A>C (p.Asn221Thr)
9g.130862875A>GCA375262685ABL1c.719A>G (p.Asn240Ser)
c.662A>G (p.Asn221Ser)
9g.130862875A>TCA375262687ABL1c.719A>T (p.Asn240Ile)
c.662A>T (p.Asn221Ile)
9g.130862876C>ACA375262690ABL1c.720C>A (p.Asn240Lys)
c.663C>A (p.Asn221Lys)
9g.130862876C>GCA375262692ABL1c.720C>G (p.Asn240Lys)
c.663C>G (p.Asn221Lys)
9g.130862876C>TCA467496259ABL1c.720C>T (p.Asn240=)
c.663C>T (p.Asn221=)

Number of alleles fetched