Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21006730T>ACA345987410APOBc.10138A>T (p.Lys3380Ter)
c.5869+4003A>T (n.5869+4003A>T)
2g.21006730T>CCA345987411APOBc.10138A>G (p.Lys3380Glu)
c.5869+4003A>G (n.5869+4003A>G)
2g.21006730T>GCA345987412APOBc.10138A>C (p.Lys3380Gln)
c.5869+4003A>C (n.5869+4003A>C)
2g.21006731G>ACA042549APOBc.10137C>T (p.Tyr3379=)
c.5869+4002C>T (n.5869+4002C>T)
dbSNP ExAC gnomAD v2
2g.21006731G>CCA345987413APOBc.10137C>G (p.Tyr3379Ter)
c.5869+4002C>G (n.5869+4002C>G)
2g.21006731G=CA2493474938APOBc.10137C= (p.Tyr3379=)
c.5869+4002C= (n.5869+4002C=)
2g.21006731G>TCA345987414APOBc.10137C>A (p.Tyr3379Ter)
c.5869+4002C>A (n.5869+4002C>A)
2g.21006732T>ACA345987415APOBc.10136A>T (p.Tyr3379Phe)
c.5869+4001A>T (n.5869+4001A>T)
2g.21006732T>CCA43496436APOBc.10136A>G (p.Tyr3379Cys)
c.5869+4001A>G (n.5869+4001A>G)
dbSNP gnomAD v4
2g.21006732T>GCA345987416APOBc.10136A>C (p.Tyr3379Ser)
c.5869+4001A>C (n.5869+4001A>C)
2g.21006732T=CA2493474939APOBc.10136A= (p.Tyr3379=)
c.5869+4001A= (n.5869+4001A=)
2g.21006733A>CCA345987417APOBc.10135T>G (p.Tyr3379Asp)
c.5869+4000T>G (n.5869+4000T>G)
2g.21006733A>GCA345987419APOBc.10135T>C (p.Tyr3379His)
c.5869+4000T>C (n.5869+4000T>C)
2g.21006733A>TCA345987418APOBc.10135T>A (p.Tyr3379Asn)
c.5869+4000T>A (n.5869+4000T>A)
2g.21006734delCA2658076562APOBc.10134del (p.Gln3378HisfsTer4)
c.5869+3999del (n.5869+3999del)
gnomAD v4
2g.21006734C>ACA345987420APOBc.10134G>T (p.Gln3378His)
c.5869+3999G>T (n.5869+3999G>T)
2g.21006734C=CA2493474940APOBc.10134G= (p.Gln3378=)
c.5869+3999G= (n.5869+3999G=)
2g.21006734C>GCA43496442APOBc.10134G>C (p.Gln3378His)
c.5869+3999G>C (n.5869+3999G>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006734C>TCA425343671APOBc.10134G>A (p.Gln3378=)
c.5869+3999G>A (n.5869+3999G>A)
dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.21006735T>ACA345987421APOBc.10133A>T (p.Gln3378Leu)
c.5869+3998A>T (n.5869+3998A>T)
2g.21006735T>CCA345987422APOBc.10133A>G (p.Gln3378Arg)
c.5869+3998A>G (n.5869+3998A>G)
2g.21006735T>GCA345987423APOBc.10133A>C (p.Gln3378Pro)
c.5869+3998A>C (n.5869+3998A>C)
2g.21006736G>ACA345987424APOBc.10132C>T (p.Gln3378Ter)
c.5869+3997C>T (n.5869+3997C>T)
2g.21006736G>CCA345987425APOBc.10132C>G (p.Gln3378Glu)
c.5869+3997C>G (n.5869+3997C>G)
2g.21006736G=CA2493474941APOBc.10132C= (p.Gln3378=)
c.5869+3997C= (n.5869+3997C=)
2g.21006736G>TCA345987426APOBc.10132C>A (p.Gln3378Lys)
c.5869+3997C>A (n.5869+3997C>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006737C>ACA425343680APOBc.10131G>T (p.Leu3377=)
c.5869+3996G>T (n.5869+3996G>T)
2g.21006737C=CA2493474942APOBc.10131G= (p.Leu3377=)
c.5869+3996G= (n.5869+3996G=)
2g.21006737C>GCA425343681APOBc.10131G>C (p.Leu3377=)
c.5869+3996G>C (n.5869+3996G>C)
2g.21006737C>TCA042539APOBc.10131G>A (p.Leu3377=)
c.5869+3996G>A (n.5869+3996G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006738A>CCA345987427APOBc.10130T>G (p.Leu3377Arg)
c.5869+3995T>G (n.5869+3995T>G)
2g.21006738A>GCA345987428APOBc.10130T>C (p.Leu3377Pro)
c.5869+3995T>C (n.5869+3995T>C)
2g.21006738A>TCA345987429APOBc.10130T>A (p.Leu3377Gln)
c.5869+3995T>A (n.5869+3995T>A)
2g.21006739G>ACA425343687APOBc.10129C>T (p.Leu3377=)
c.5869+3994C>T (n.5869+3994C>T)
2g.21006739G>CCA345987431APOBc.10129C>G (p.Leu3377Val)
c.5869+3994C>G (n.5869+3994C>G)
ClinVar
2g.21006739G=CA2493474943APOBc.10129C= (p.Leu3377=)
c.5869+3994C= (n.5869+3994C=)
2g.21006739G>TCA345987430APOBc.10129C>A (p.Leu3377Met)
c.5869+3994C>A (n.5869+3994C>A)
ClinVar dbSNP gnomAD v4
2g.21006740T>ACA425343689APOBc.10128A>T (p.Ala3376=)
c.5869+3993A>T (n.5869+3993A>T)
COSMIC
2g.21006740T>CCA10614157APOBc.10128A>G (p.Ala3376=)
c.5869+3993A>G (n.5869+3993A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006740T>GCA425343691APOBc.10128A>C (p.Ala3376=)
c.5869+3993A>C (n.5869+3993A>C)
dbSNP
2g.21006740T=CA2493474944APOBc.10128A= (p.Ala3376=)
c.5869+3993A= (n.5869+3993A=)
2g.21006741G>ACA43496466APOBc.10127C>T (p.Ala3376Val)
c.5869+3992C>T (n.5869+3992C>T)
dbSNP
2g.21006741G>CCA345987432APOBc.10127C>G (p.Ala3376Gly)
c.5869+3992C>G (n.5869+3992C>G)
2g.21006741G=CA2493474945APOBc.10127C= (p.Ala3376=)
c.5869+3992C= (n.5869+3992C=)
2g.21006741G>TCA042512APOBc.10127C>A (p.Ala3376Glu)
c.5869+3992C>A (n.5869+3992C>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006742C>ACA345987433APOBc.10126G>T (p.Ala3376Ser)
c.5869+3991G>T (n.5869+3991G>T)
ClinVar
2g.21006742C=CA2493474946APOBc.10126G= (p.Ala3376=)
c.5869+3991G= (n.5869+3991G=)
2g.21006742C>GCA345987434APOBc.10126G>C (p.Ala3376Pro)
c.5869+3991G>C (n.5869+3991G>C)
2g.21006742C>TCA345987435APOBc.10126G>A (p.Ala3376Thr)
c.5869+3991G>A (n.5869+3991G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21006743A=CA2493474947APOBc.10125T= (p.Asp3375=)
c.5869+3990T= (n.5869+3990T=)
2g.21006743A>CCA345987436APOBc.10125T>G (p.Asp3375Glu)
c.5869+3990T>G (n.5869+3990T>G)
2g.21006743A>GCA425343695APOBc.10125T>C (p.Asp3375=)
c.5869+3990T>C (n.5869+3990T>C)
ClinVar dbSNP gnomAD v4
2g.21006743A>TCA345987437APOBc.10125T>A (p.Asp3375Glu)
c.5869+3990T>A (n.5869+3990T>A)
2g.21006744T>ACA43496467APOBc.10124A>T (p.Asp3375Val)
c.5869+3989A>T (n.5869+3989A>T)
dbSNP
2g.21006744T>CCA345987438APOBc.10124A>G (p.Asp3375Gly)
c.5869+3989A>G (n.5869+3989A>G)
gnomAD v4
2g.21006744T>GCA345987439APOBc.10124A>C (p.Asp3375Ala)
c.5869+3989A>C (n.5869+3989A>C)
2g.21006744T=CA2493474948APOBc.10124A= (p.Asp3375=)
c.5869+3989A= (n.5869+3989A=)
2g.21006745C>ACA345987442APOBc.10123G>T (p.Asp3375Tyr)
c.5869+3988G>T (n.5869+3988G>T)
2g.21006745C=CA2493474949APOBc.10123G= (p.Asp3375=)
c.5869+3988G= (n.5869+3988G=)
2g.21006745C>GCA345987441APOBc.10123G>C (p.Asp3375His)
c.5869+3988G>C (n.5869+3988G>C)
2g.21006745C>TCA345987440APOBc.10123G>A (p.Asp3375Asn)
c.5869+3988G>A (n.5869+3988G>A)
dbSNP
2g.21006746A=CA2493474950APOBc.10122T= (p.Ile3374=)
c.5869+3987T= (n.5869+3987T=)
2g.21006746A>CCA345987443APOBc.10122T>G (p.Ile3374Met)
c.5869+3987T>G (n.5869+3987T>G)
dbSNP
2g.21006746A>GCA042491APOBc.10122T>C (p.Ile3374=)
c.5869+3987T>C (n.5869+3987T>C)
dbSNP ExAC gnomAD v2
2g.21006746A>TCA425343698APOBc.10122T>A (p.Ile3374=)
c.5869+3987T>A (n.5869+3987T>A)
gnomAD v4
2g.21006747delCA2576686509APOBc.10122del (p.Ile3374MetfsTer8)
c.5869+3987del (n.5869+3987del)
2g.21006747A=CA2493474951APOBc.10121T= (p.Ile3374=)
c.5869+3986T= (n.5869+3986T=)
2g.21006747A>CCA345987444APOBc.10121T>G (p.Ile3374Ser)
c.5869+3986T>G (n.5869+3986T>G)
2g.21006747A>GCA43496478APOBc.10121T>C (p.Ile3374Thr)
c.5869+3986T>C (n.5869+3986T>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006747A>TCA345987445APOBc.10121T>A (p.Ile3374Asn)
c.5869+3986T>A (n.5869+3986T>A)
2g.21006748T>ACA345987446APOBc.10120A>T (p.Ile3374Phe)
c.5869+3985A>T (n.5869+3985A>T)
ClinVar
2g.21006748T>CCA345987448APOBc.10120A>G (p.Ile3374Val)
c.5869+3985A>G (n.5869+3985A>G)
2g.21006748T>GCA345987447APOBc.10120A>C (p.Ile3374Leu)
c.5869+3985A>C (n.5869+3985A>C)
2g.21006749G>ACA425343705APOBc.10119C>T (p.Val3373=)
c.5869+3984C>T (n.5869+3984C>T)
gnomAD v4
2g.21006749G>CCA425343706APOBc.10119C>G (p.Val3373=)
c.5869+3984C>G (n.5869+3984C>G)
2g.21006749G>TCA425343707APOBc.10119C>A (p.Val3373=)
c.5869+3984C>A (n.5869+3984C>A)
2g.21006750A>CCA345987449APOBc.10118T>G (p.Val3373Gly)
c.5869+3983T>G (n.5869+3983T>G)
2g.21006750A>GCA345987450APOBc.10118T>C (p.Val3373Ala)
c.5869+3983T>C (n.5869+3983T>C)
2g.21006750A>TCA345987451APOBc.10118T>A (p.Val3373Asp)
c.5869+3983T>A (n.5869+3983T>A)
2g.21006751C>ACA345987452APOBc.10117G>T (p.Val3373Phe)
c.5869+3982G>T (n.5869+3982G>T)
2g.21006751C=CA2493474952APOBc.10117G= (p.Val3373=)
c.5869+3982G= (n.5869+3982G=)
2g.21006751C>GCA042477APOBc.10117G>C (p.Val3373Leu)
c.5869+3982G>C (n.5869+3982G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006751C>TCA345987453APOBc.10117G>A (p.Val3373Ile)
c.5869+3982G>A (n.5869+3982G>A)
gnomAD v4
2g.21006751_21006757delinsCAGATGACA2493474953APOBc.10111_10117delinsTCATCTG (p.Ser3371=)
c.5869+3976_5869+3982delinsTCATCTG (n.5869+3976_5869+3982delinsTCATCTG)
2g.21006752A=CA2493474954APOBc.10116T= (p.Ser3372=)
c.5869+3981T= (n.5869+3981T=)
2g.21006752A>CCA425343714APOBc.10116T>G (p.Ser3372=)
c.5869+3981T>G (n.5869+3981T>G)
2g.21006752A>GCA042462APOBc.10116T>C (p.Ser3372=)
c.5869+3981T>C (n.5869+3981T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006752A>TCA425343718APOBc.10116T>A (p.Ser3372=)
c.5869+3981T>A (n.5869+3981T>A)
2g.21006761_21006766delCA531312732APOBc.10111_10116del (p.Ser3371_Ser3372del)
c.5869+3976_5869+3981del (n.5869+3976_5869+3981del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006753G>ACA345987454APOBc.10115C>T (p.Ser3372Phe)
c.5869+3980C>T (n.5869+3980C>T)
dbSNP
2g.21006753G>CCA345987455APOBc.10115C>G (p.Ser3372Cys)
c.5869+3980C>G (n.5869+3980C>G)
2g.21006753G=CA2493474955APOBc.10115C= (p.Ser3372=)
c.5869+3980C= (n.5869+3980C=)
2g.21006753G>TCA345987456APOBc.10115C>A (p.Ser3372Tyr)
c.5869+3980C>A (n.5869+3980C>A)
2g.21006754A=CA2493474956APOBc.10114T= (p.Ser3372=)
c.5869+3979T= (n.5869+3979T=)
2g.21006754A>CCA042447APOBc.10114T>G (p.Ser3372Ala)
c.5869+3979T>G (n.5869+3979T>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006754A>GCA43496490APOBc.10114T>C (p.Ser3372Pro)
c.5869+3979T>C (n.5869+3979T>C)
dbSNP
2g.21006754A>TCA345987457APOBc.10114T>A (p.Ser3372Thr)
c.5869+3979T>A (n.5869+3979T>A)
2g.21006755T>ACA43496491APOBc.10113A>T (p.Ser3371=)
c.5869+3978A>T (n.5869+3978A>T)
dbSNP gnomAD v2 gnomAD v4
2g.21006755T>CCA425343724APOBc.10113A>G (p.Ser3371=)
c.5869+3978A>G (n.5869+3978A>G)
gnomAD v4
2g.21006755T>GCA425343725APOBc.10113A>C (p.Ser3371=)
c.5869+3978A>C (n.5869+3978A>C)
2g.21006755T=CA2493474957APOBc.10113A= (p.Ser3371=)
c.5869+3978A= (n.5869+3978A=)
2g.21006756G>ACA345987460APOBc.10112C>T (p.Ser3371Leu)
c.5869+3977C>T (n.5869+3977C>T)
2g.21006756G>CCA345987458APOBc.10112C>G (p.Ser3371Ter)
c.5869+3977C>G (n.5869+3977C>G)
2g.21006756G>TCA345987459APOBc.10112C>A (p.Ser3371Ter)
c.5869+3977C>A (n.5869+3977C>A)
2g.21006757A>CCA345987461APOBc.10111T>G (p.Ser3371Ala)
c.5869+3976T>G (n.5869+3976T>G)
2g.21006757A>GCA345987462APOBc.10111T>C (p.Ser3371Pro)
c.5869+3976T>C (n.5869+3976T>C)
2g.21006757A>TCA345987463APOBc.10111T>A (p.Ser3371Thr)
c.5869+3976T>A (n.5869+3976T>A)
2g.21006758A>CCA425343732APOBc.10110T>G (p.Ser3370=)
c.5869+3975T>G (n.5869+3975T>G)
2g.21006758A>GCA425343733APOBc.10110T>C (p.Ser3370=)
c.5869+3975T>C (n.5869+3975T>C)
2g.21006758A>TCA425343734APOBc.10110T>A (p.Ser3370=)
c.5869+3975T>A (n.5869+3975T>A)
2g.21006759G>ACA345987464APOBc.10109C>T (p.Ser3370Phe)
c.5869+3974C>T (n.5869+3974C>T)
dbSNP
2g.21006759G>CCA345987465APOBc.10109C>G (p.Ser3370Cys)
c.5869+3974C>G (n.5869+3974C>G)
2g.21006759G=CA2493474958APOBc.10109C= (p.Ser3370=)
c.5869+3974C= (n.5869+3974C=)
2g.21006759G>TCA345987466APOBc.10109C>A (p.Ser3370Tyr)
c.5869+3974C>A (n.5869+3974C>A)
2g.21006760A>CCA345987467APOBc.10108T>G (p.Ser3370Ala)
c.5869+3973T>G (n.5869+3973T>G)
2g.21006760A>GCA345987468APOBc.10108T>C (p.Ser3370Pro)
c.5869+3973T>C (n.5869+3973T>C)
gnomAD v4
2g.21006760A>TCA345987469APOBc.10108T>A (p.Ser3370Thr)
c.5869+3973T>A (n.5869+3973T>A)
2g.21006761T>ACA425343736APOBc.10107A>T (p.Ser3369=)
c.5869+3972A>T (n.5869+3972A>T)
2g.21006761T>CCA425343737APOBc.10107A>G (p.Ser3369=)
c.5869+3972A>G (n.5869+3972A>G)
ClinVar gnomAD v4
2g.21006761T>GCA425343738APOBc.10107A>C (p.Ser3369=)
c.5869+3972A>C (n.5869+3972A>C)
dbSNP
2g.21006761T=CA2493474959APOBc.10107A= (p.Ser3369=)
c.5869+3972A= (n.5869+3972A=)
2g.21006762G>ACA345987470APOBc.10106C>T (p.Ser3369Leu)
c.5869+3971C>T (n.5869+3971C>T)
2g.21006762G>CCA345987471APOBc.10106C>G (p.Ser3369Ter)
c.5869+3971C>G (n.5869+3971C>G)
2g.21006762G>TCA345987472APOBc.10106C>A (p.Ser3369Ter)
c.5869+3971C>A (n.5869+3971C>A)
2g.21006765_21006767delCA645523820APOBc.10104_10106del (p.Ser3369del)
c.5869+3969_5869+3971del (n.5869+3969_5869+3971del)
COSMIC
2g.21006763A>CCA345987473APOBc.10105T>G (p.Ser3369Ala)
c.5869+3970T>G (n.5869+3970T>G)
2g.21006763A>GCA345987475APOBc.10105T>C (p.Ser3369Pro)
c.5869+3970T>C (n.5869+3970T>C)
gnomAD v4
2g.21006763A>TCA345987474APOBc.10105T>A (p.Ser3369Thr)
c.5869+3970T>A (n.5869+3970T>A)
2g.21006763_21006781delinsAAGAAAGGAGATGAGCAACCA2493474960APOBc.10087_10105delinsGTTGCTCATCTCCTTTCTT (p.Val3363=)
c.5869+3952_5869+3970delinsGTTGCTCATCTCCTTTCTT (n.5869+3952_5869+3970delinsGTTGCTCATCTCCTTTCTT)
2g.21006764A>CCA425343741APOBc.10104T>G (p.Ser3368=)
c.5869+3969T>G (n.5869+3969T>G)
2g.21006764A>GCA425343743APOBc.10104T>C (p.Ser3368=)
c.5869+3969T>C (n.5869+3969T>C)
2g.21006764A>TCA425343745APOBc.10104T>A (p.Ser3368=)
c.5869+3969T>A (n.5869+3969T>A)
2g.21006765_21006782delCA531312733APOBc.10087_10104del (p.Val3363_Ser3368del)
c.5869+3952_5869+3969del (n.5869+3952_5869+3969del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006765G>ACA042422APOBc.10103C>T (p.Ser3368Phe)
c.5869+3968C>T (n.5869+3968C>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006765G>CCA345987476APOBc.10103C>G (p.Ser3368Cys)
c.5869+3968C>G (n.5869+3968C>G)
2g.21006765G=CA2493474961APOBc.10103C= (p.Ser3368=)
c.5869+3968C= (n.5869+3968C=)
2g.21006765G>TCA345987477APOBc.10103C>A (p.Ser3368Tyr)
c.5869+3968C>A (n.5869+3968C>A)
2g.21006766A>CCA345987478APOBc.10102T>G (p.Ser3368Ala)
c.5869+3967T>G (n.5869+3967T>G)
2g.21006766A>GCA345987479APOBc.10102T>C (p.Ser3368Pro)
c.5869+3967T>C (n.5869+3967T>C)
2g.21006766A>TCA345987480APOBc.10102T>A (p.Ser3368Thr)
c.5869+3967T>A (n.5869+3967T>A)
2g.21006767A=CA2493474962APOBc.10101T= (p.Leu3367=)
c.5869+3966T= (n.5869+3966T=)
2g.21006767A>CCA425343755APOBc.10101T>G (p.Leu3367=)
c.5869+3966T>G (n.5869+3966T>G)
2g.21006767A>GCA042409APOBc.10101T>C (p.Leu3367=)
c.5869+3966T>C (n.5869+3966T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006767A>TCA425343751APOBc.10101T>A (p.Leu3367=)
c.5869+3966T>A (n.5869+3966T>A)
2g.21006768A>CCA345987481APOBc.10100T>G (p.Leu3367Arg)
c.5869+3965T>G (n.5869+3965T>G)
2g.21006768A>GCA345987482APOBc.10100T>C (p.Leu3367Pro)
c.5869+3965T>C (n.5869+3965T>C)
gnomAD v4
2g.21006768A>TCA345987483APOBc.10100T>A (p.Leu3367His)
c.5869+3965T>A (n.5869+3965T>A)
2g.21006770_21006772delCA2573051851APOBc.10098_10100del (p.Leu3367del)
c.5869+3963_5869+3965del (n.5869+3963_5869+3965del)
ClinVar dbSNP
2g.21006769G>ACA345987486APOBc.10099C>T (p.Leu3367Phe)
c.5869+3964C>T (n.5869+3964C>T)
2g.21006769G>CCA345987485APOBc.10099C>G (p.Leu3367Val)
c.5869+3964C>G (n.5869+3964C>G)
2g.21006769G>TCA345987484APOBc.10099C>A (p.Leu3367Ile)
c.5869+3964C>A (n.5869+3964C>A)
2g.21006770G>ACA425343762APOBc.10098C>T (p.Leu3366=)
c.5869+3963C>T (n.5869+3963C>T)
ClinVar dbSNP COSMIC
2g.21006770G>CCA425343760APOBc.10098C>G (p.Leu3366=)
c.5869+3963C>G (n.5869+3963C>G)
2g.21006770G=CA2493474963APOBc.10098C= (p.Leu3366=)
c.5869+3963C= (n.5869+3963C=)
2g.21006770G>TCA425343758APOBc.10098C>A (p.Leu3366=)
c.5869+3963C>A (n.5869+3963C>A)
2g.21006771A=CA2493474964APOBc.10097T= (p.Leu3366=)
c.5869+3962T= (n.5869+3962T=)
2g.21006771A>CCA345987487APOBc.10097T>G (p.Leu3366Arg)
c.5869+3962T>G (n.5869+3962T>G)
2g.21006771A>GCA345987488APOBc.10097T>C (p.Leu3366Pro)
c.5869+3962T>C (n.5869+3962T>C)
gnomAD v4
2g.21006771A>TCA345987489APOBc.10097T>A (p.Leu3366His)
c.5869+3962T>A (n.5869+3962T>A)
dbSNP
2g.21006772delCA2593838322APOBc.10096del (p.Leu3366SerfsTer16)
c.5869+3961del (n.5869+3961del)
gnomAD v3 gnomAD v4
2g.21006772G>ACA345987490APOBc.10096C>T (p.Leu3366Phe)
c.5869+3961C>T (n.5869+3961C>T)
dbSNP
2g.21006772G>CCA345987491APOBc.10096C>G (p.Leu3366Val)
c.5869+3961C>G (n.5869+3961C>G)
2g.21006772G=CA2493474965APOBc.10096C= (p.Leu3366=)
c.5869+3961C= (n.5869+3961C=)
2g.21006772G>TCA345987492APOBc.10096C>A (p.Leu3366Ile)
c.5869+3961C>A (n.5869+3961C>A)
COSMIC
2g.21006773A>CCA345987493APOBc.10095T>G (p.His3365Gln)
c.5869+3960T>G (n.5869+3960T>G)
2g.21006773A>GCA425343768APOBc.10095T>C (p.His3365=)
c.5869+3960T>C (n.5869+3960T>C)
gnomAD v4
2g.21006773A>TCA345987494APOBc.10095T>A (p.His3365Gln)
c.5869+3960T>A (n.5869+3960T>A)
2g.21006774T>ACA345987495APOBc.10094A>T (p.His3365Leu)
c.5869+3959A>T (n.5869+3959A>T)
gnomAD v4
2g.21006774T>CCA345987496APOBc.10094A>G (p.His3365Arg)
c.5869+3959A>G (n.5869+3959A>G)
dbSNP gnomAD v3 gnomAD v4
2g.21006774T>GCA345987497APOBc.10094A>C (p.His3365Pro)
c.5869+3959A>C (n.5869+3959A>C)
gnomAD v4
2g.21006774T=CA2493474966APOBc.10094A= (p.His3365=)
c.5869+3959A= (n.5869+3959A=)
2g.21006775G>ACA345987500APOBc.10093C>T (p.His3365Tyr)
c.5869+3958C>T (n.5869+3958C>T)
gnomAD v4
2g.21006775G>CCA345987499APOBc.10093C>G (p.His3365Asp)
c.5869+3958C>G (n.5869+3958C>G)
dbSNP
2g.21006775G=CA2493474967APOBc.10093C= (p.His3365=)
c.5869+3958C= (n.5869+3958C=)
2g.21006775G>TCA345987498APOBc.10093C>A (p.His3365Asn)
c.5869+3958C>A (n.5869+3958C>A)
2g.21006776A=CA2493474968APOBc.10092T= (p.Ala3364=)
c.5869+3957T= (n.5869+3957T=)
2g.21006776A>CCA425343771APOBc.10092T>G (p.Ala3364=)
c.5869+3957T>G (n.5869+3957T>G)
2g.21006776A>GCA425343778APOBc.10092T>C (p.Ala3364=)
c.5869+3957T>C (n.5869+3957T>C)
dbSNP gnomAD v4
2g.21006776A>TCA425343780APOBc.10092T>A (p.Ala3364=)
c.5869+3957T>A (n.5869+3957T>A)
2g.21006777G>ACA345987502APOBc.10091C>T (p.Ala3364Val)
c.5869+3956C>T (n.5869+3956C>T)
2g.21006777G>CCA345987506APOBc.10091C>G (p.Ala3364Gly)
c.5869+3956C>G (n.5869+3956C>G)
2g.21006777G>TCA345987504APOBc.10091C>A (p.Ala3364Asp)
c.5869+3956C>A (n.5869+3956C>A)
2g.21006778C>ACA345987508APOBc.10090G>T (p.Ala3364Ser)
c.5869+3955G>T (n.5869+3955G>T)
gnomAD v4
2g.21006778C>GCA345987510APOBc.10090G>C (p.Ala3364Pro)
c.5869+3955G>C (n.5869+3955G>C)
2g.21006778C>TCA345987512APOBc.10090G>A (p.Ala3364Thr)
c.5869+3955G>A (n.5869+3955G>A)
gnomAD v4
2g.21006779A>CCA425343784APOBc.10089T>G (p.Val3363=)
c.5869+3954T>G (n.5869+3954T>G)
2g.21006779A>GCA425343786APOBc.10089T>C (p.Val3363=)
c.5869+3954T>C (n.5869+3954T>C)
2g.21006779A>TCA425343787APOBc.10089T>A (p.Val3363=)
c.5869+3954T>A (n.5869+3954T>A)
2g.21006780A>CCA345987514APOBc.10088T>G (p.Val3363Gly)
c.5869+3953T>G (n.5869+3953T>G)
2g.21006780A>GCA345987516APOBc.10088T>C (p.Val3363Ala)
c.5869+3953T>C (n.5869+3953T>C)
2g.21006780A>TCA345987518APOBc.10088T>A (p.Val3363Asp)
c.5869+3953T>A (n.5869+3953T>A)
ClinVar
2g.21006781C>ACA345987521APOBc.10087G>T (p.Val3363Phe)
c.5869+3952G>T (n.5869+3952G>T)
2g.21006781C>GCA345987522APOBc.10087G>C (p.Val3363Leu)
c.5869+3952G>C (n.5869+3952G>C)
2g.21006781C>TCA345987524APOBc.10087G>A (p.Val3363Ile)
c.5869+3952G>A (n.5869+3952G>A)
2g.21006782A=CA2493474969APOBc.10086T= (p.Ile3362=)
c.5869+3951T= (n.5869+3951T=)
2g.21006782A>CCA345987526APOBc.10086T>G (p.Ile3362Met)
c.5869+3951T>G (n.5869+3951T>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21006782A>GCA425343794APOBc.10086T>C (p.Ile3362=)
c.5869+3951T>C (n.5869+3951T>C)
dbSNP
2g.21006782A>TCA425343795APOBc.10086T>A (p.Ile3362=)
c.5869+3951T>A (n.5869+3951T>A)
2g.21006783A>CCA345987532APOBc.10085T>G (p.Ile3362Ser)
c.5869+3950T>G (n.5869+3950T>G)
2g.21006783A>GCA345987530APOBc.10085T>C (p.Ile3362Thr)
c.5869+3950T>C (n.5869+3950T>C)
gnomAD v4
2g.21006783A>TCA345987529APOBc.10085T>A (p.Ile3362Asn)
c.5869+3950T>A (n.5869+3950T>A)
2g.21006783_21006784insATTTGTGGAGGGTAGTCATAACAGCA2548971132APOBc.10084_10085insCTGTTATGACTACCCTCCACAAAT (p.Ile3362delinsThrValMetThrThrLeuHisLysPhe)
c.5869+3949_5869+3950insCTGTTATGACTACCCTCCACAAAT (n.5869+3949_5869+3950insCTGTTATGACTACCCTCCACAAAT)
2g.21006784T>ACA345987535APOBc.10084A>T (p.Ile3362Phe)
c.5869+3949A>T (n.5869+3949A>T)
2g.21006784T>CCA345987536APOBc.10084A>G (p.Ile3362Val)
c.5869+3949A>G (n.5869+3949A>G)
gnomAD v4
2g.21006784T>GCA345987538APOBc.10084A>C (p.Ile3362Leu)
c.5869+3949A>C (n.5869+3949A>C)
2g.21006785A>CCA345987541APOBc.10083T>G (p.Asp3361Glu)
c.5869+3948T>G (n.5869+3948T>G)
2g.21006785A>GCA425343801APOBc.10083T>C (p.Asp3361=)
c.5869+3948T>C (n.5869+3948T>C)
2g.21006785A>TCA345987542APOBc.10083T>A (p.Asp3361Glu)
c.5869+3948T>A (n.5869+3948T>A)
2g.21006786T>ACA345987545APOBc.10082A>T (p.Asp3361Val)
c.5869+3947A>T (n.5869+3947A>T)
2g.21006786T>CCA345987546APOBc.10082A>G (p.Asp3361Gly)
c.5869+3947A>G (n.5869+3947A>G)
2g.21006786T>GCA345987548APOBc.10082A>C (p.Asp3361Ala)
c.5869+3947A>C (n.5869+3947A>C)
2g.21006787C>ACA43496513APOBc.10081G>T (p.Asp3361Tyr)
c.5869+3946G>T (n.5869+3946G>T)
dbSNP
2g.21006787C=CA2493474970APOBc.10081G= (p.Asp3361=)
c.5869+3946G= (n.5869+3946G=)
2g.21006787C>GCA345987552APOBc.10081G>C (p.Asp3361His)
c.5869+3946G>C (n.5869+3946G>C)
2g.21006787C>TCA345987554APOBc.10081G>A (p.Asp3361Asn)
c.5869+3946G>A (n.5869+3946G>A)
dbSNP gnomAD v3 gnomAD v4
2g.21006788T>ACA425343813APOBc.10080A>T (p.Ser3360=)
c.5869+3945A>T (n.5869+3945A>T)
2g.21006788T>CCA425343819APOBc.10080A>G (p.Ser3360=)
c.5869+3945A>G (n.5869+3945A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21006788T>GCA425343820APOBc.10080A>C (p.Ser3360=)
c.5869+3945A>C (n.5869+3945A>C)
2g.21006788T=CA2493474971APOBc.10080A= (p.Ser3360=)
c.5869+3945A= (n.5869+3945A=)
2g.21006789G>ACA345987559APOBc.10079C>T (p.Ser3360Leu)
c.5869+3944C>T (n.5869+3944C>T)
2g.21006789G>CCA345987561APOBc.10079C>G (p.Ser3360Ter)
c.5869+3944C>G (n.5869+3944C>G)
2g.21006789G>TCA345987556APOBc.10079C>A (p.Ser3360Ter)
c.5869+3944C>A (n.5869+3944C>A)
2g.21006790A>CCA345987563APOBc.10078T>G (p.Ser3360Ala)
c.5869+3943T>G (n.5869+3943T>G)
2g.21006790A>GCA345987565APOBc.10078T>C (p.Ser3360Pro)
c.5869+3943T>C (n.5869+3943T>C)
2g.21006790A>TCA345987567APOBc.10078T>A (p.Ser3360Thr)
c.5869+3943T>A (n.5869+3943T>A)
2g.21006791C>ACA345987570APOBc.10077G>T (p.Gln3359His)
c.5869+3942G>T (n.5869+3942G>T)
2g.21006791C=CA2493474972APOBc.10077G= (p.Gln3359=)
c.5869+3942G= (n.5869+3942G=)
2g.21006791C>GCA345987572APOBc.10077G>C (p.Gln3359His)
c.5869+3942G>C (n.5869+3942G>C)
2g.21006791C>TCA43496521APOBc.10077G>A (p.Gln3359=)
c.5869+3942G>A (n.5869+3942G>A)
dbSNP
2g.21006792T>ACA43496531APOBc.10076A>T (p.Gln3359Leu)
c.5869+3941A>T (n.5869+3941A>T)
dbSNP gnomAD v4
2g.21006792T>CCA345987577APOBc.10076A>G (p.Gln3359Arg)
c.5869+3941A>G (n.5869+3941A>G)
2g.21006792T>GCA345987578APOBc.10076A>C (p.Gln3359Pro)
c.5869+3941A>C (n.5869+3941A>C)
2g.21006792T=CA2493474973APOBc.10076A= (p.Gln3359=)
c.5869+3941A= (n.5869+3941A=)
2g.21006793G>ACA345987581APOBc.10075C>T (p.Gln3359Ter)
c.5869+3940C>T (n.5869+3940C>T)
2g.21006793G>CCA345987583APOBc.10075C>G (p.Gln3359Glu)
c.5869+3940C>G (n.5869+3940C>G)
2g.21006793G>TCA345987584APOBc.10075C>A (p.Gln3359Lys)
c.5869+3940C>A (n.5869+3940C>A)
2g.21006794G>ACA425343844APOBc.10074C>T (p.Asn3358=)
c.5869+3939C>T (n.5869+3939C>T)
dbSNP
2g.21006794G>CCA345987589APOBc.10074C>G (p.Asn3358Lys)
c.5869+3939C>G (n.5869+3939C>G)
dbSNP
2g.21006794G=CA2493474974APOBc.10074C= (p.Asn3358=)
c.5869+3939C= (n.5869+3939C=)
2g.21006794G>TCA345987587APOBc.10074C>A (p.Asn3358Lys)
c.5869+3939C>A (n.5869+3939C>A)
2g.21006795T>ACA345987591APOBc.10073A>T (p.Asn3358Ile)
c.5869+3938A>T (n.5869+3938A>T)
2g.21006795T>CCA345987593APOBc.10073A>G (p.Asn3358Ser)
c.5869+3938A>G (n.5869+3938A>G)
ClinVar dbSNP gnomAD v4
2g.21006795T>GCA345987595APOBc.10073A>C (p.Asn3358Thr)
c.5869+3938A>C (n.5869+3938A>C)
gnomAD v4
2g.21006796T>ACA345987598APOBc.10072A>T (p.Asn3358Tyr)
c.5869+3937A>T (n.5869+3937A>T)
2g.21006796T>CCA345987600APOBc.10072A>G (p.Asn3358Asp)
c.5869+3937A>G (n.5869+3937A>G)
2g.21006796T>GCA345987602APOBc.10072A>C (p.Asn3358His)
c.5869+3937A>C (n.5869+3937A>C)
ClinVar dbSNP
2g.21006796T=CA2493474975APOBc.10072A= (p.Asn3358=)
c.5869+3937A= (n.5869+3937A=)
2g.21006797A>CCA345987604APOBc.10071T>G (p.Phe3357Leu)
c.5869+3936T>G (n.5869+3936T>G)
2g.21006797A>GCA425343851APOBc.10071T>C (p.Phe3357=)
c.5869+3936T>C (n.5869+3936T>C)
2g.21006797A>TCA345987607APOBc.10071T>A (p.Phe3357Leu)
c.5869+3936T>A (n.5869+3936T>A)
2g.21006798A=CA2493474976APOBc.10070T= (p.Phe3357=)
c.5869+3935T= (n.5869+3935T=)
2g.21006798A>CCA345987609APOBc.10070T>G (p.Phe3357Cys)
c.5869+3935T>G (n.5869+3935T>G)
2g.21006798A>GCA345987611APOBc.10070T>C (p.Phe3357Ser)
c.5869+3935T>C (n.5869+3935T>C)
2g.21006798A>TCA345987613APOBc.10070T>A (p.Phe3357Tyr)
c.5869+3935T>A (n.5869+3935T>A)
dbSNP
2g.21006799A>CCA345987616APOBc.10069T>G (p.Phe3357Val)
c.5869+3934T>G (n.5869+3934T>G)
2g.21006799A>GCA345987618APOBc.10069T>C (p.Phe3357Leu)
c.5869+3934T>C (n.5869+3934T>C)
dbSNP
2g.21006799A>TCA345987620APOBc.10069T>A (p.Phe3357Ile)
c.5869+3934T>A (n.5869+3934T>A)
2g.21006800A>CCA425343854APOBc.10068T>G (p.Leu3356=)
c.5869+3933T>G (n.5869+3933T>G)
2g.21006800A>GCA425343857APOBc.10068T>C (p.Leu3356=)
c.5869+3933T>C (n.5869+3933T>C)
gnomAD v4
2g.21006800A>TCA425343855APOBc.10068T>A (p.Leu3356=)
c.5869+3933T>A (n.5869+3933T>A)
2g.21006801A>CCA345987625APOBc.10067T>G (p.Leu3356Arg)
c.5869+3932T>G (n.5869+3932T>G)
2g.21006801A>GCA345987627APOBc.10067T>C (p.Leu3356Pro)
c.5869+3932T>C (n.5869+3932T>C)
2g.21006801A>TCA345987623APOBc.10067T>A (p.Leu3356His)
c.5869+3932T>A (n.5869+3932T>A)
2g.21006802G>ACA345987631APOBc.10066C>T (p.Leu3356Phe)
c.5869+3931C>T (n.5869+3931C>T)
gnomAD v4
2g.21006802G>CCA43496537APOBc.10066C>G (p.Leu3356Val)
c.5869+3931C>G (n.5869+3931C>G)
dbSNP gnomAD v3 gnomAD v4
2g.21006802G=CA2493474977APOBc.10066C= (p.Leu3356=)
c.5869+3931C= (n.5869+3931C=)
2g.21006802G>TCA345987632APOBc.10066C>A (p.Leu3356Ile)
c.5869+3931C>A (n.5869+3931C>A)
2g.21006803T>ACA345987635APOBc.10065A>T (p.Glu3355Asp)
c.5869+3930A>T (n.5869+3930A>T)
2g.21006803T>CCA425343863APOBc.10065A>G (p.Glu3355=)
c.5869+3930A>G (n.5869+3930A>G)
2g.21006803T>GCA345987637APOBc.10065A>C (p.Glu3355Asp)
c.5869+3930A>C (n.5869+3930A>C)
dbSNP
2g.21006803T=CA2493474978APOBc.10065A= (p.Glu3355=)
c.5869+3930A= (n.5869+3930A=)
2g.21006804T>ACA345987640APOBc.10064A>T (p.Glu3355Val)
c.5869+3929A>T (n.5869+3929A>T)
2g.21006804T>CCA345987641APOBc.10064A>G (p.Glu3355Gly)
c.5869+3929A>G (n.5869+3929A>G)
dbSNP
2g.21006804T>GCA345987643APOBc.10064A>C (p.Glu3355Ala)
c.5869+3929A>C (n.5869+3929A>C)
2g.21006804T=CA2493474979APOBc.10064A= (p.Glu3355=)
c.5869+3929A= (n.5869+3929A=)
2g.21006805C>ACA345987646APOBc.10063G>T (p.Glu3355Ter)
c.5869+3928G>T (n.5869+3928G>T)
2g.21006805C=CA2493474980APOBc.10063G= (p.Glu3355=)
c.5869+3928G= (n.5869+3928G=)
2g.21006805C>GCA345987647APOBc.10063G>C (p.Glu3355Gln)
c.5869+3928G>C (n.5869+3928G>C)
2g.21006805C>TCA042366APOBc.10063G>A (p.Glu3355Lys)
c.5869+3928G>A (n.5869+3928G>A)
dbSNP ExAC gnomAD v4
2g.21006806A>CCA425343868APOBc.10062T>G (p.Ala3354=)
c.5869+3927T>G (n.5869+3927T>G)
2g.21006806A>GCA425343870APOBc.10062T>C (p.Ala3354=)
c.5869+3927T>C (n.5869+3927T>C)
2g.21006806A>TCA425343871APOBc.10062T>A (p.Ala3354=)
c.5869+3927T>A (n.5869+3927T>A)
2g.21006807G>ACA345987652APOBc.10061C>T (p.Ala3354Val)
c.5869+3926C>T (n.5869+3926C>T)
gnomAD v4 COSMIC
2g.21006807G>CCA042354APOBc.10061C>G (p.Ala3354Gly)
c.5869+3926C>G (n.5869+3926C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006807G=CA2493474981APOBc.10061C= (p.Ala3354=)
c.5869+3926C= (n.5869+3926C=)
2g.21006807G>TCA345987655APOBc.10061C>A (p.Ala3354Asp)
c.5869+3926C>A (n.5869+3926C>A)
2g.21006808C>ACA345987658APOBc.10060G>T (p.Ala3354Ser)
c.5869+3925G>T (n.5869+3925G>T)
2g.21006808C>GCA345987659APOBc.10060G>C (p.Ala3354Pro)
c.5869+3925G>C (n.5869+3925G>C)
2g.21006808C>TCA345987661APOBc.10060G>A (p.Ala3354Thr)
c.5869+3925G>A (n.5869+3925G>A)
ClinVar gnomAD v4
2g.21006809A=CA2493474982APOBc.10059T= (p.Asn3353=)
c.5869+3924T= (n.5869+3924T=)
2g.21006809A>CCA345987663APOBc.10059T>G (p.Asn3353Lys)
c.5869+3924T>G (n.5869+3924T>G)
2g.21006809A>GCA425343877APOBc.10059T>C (p.Asn3353=)
c.5869+3924T>C (n.5869+3924T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006809A>TCA345987665APOBc.10059T>A (p.Asn3353Lys)
c.5869+3924T>A (n.5869+3924T>A)
gnomAD v4
2g.21006810T>ACA345987668APOBc.10058A>T (p.Asn3353Ile)
c.5869+3923A>T (n.5869+3923A>T)
2g.21006810T>CCA345987669APOBc.10058A>G (p.Asn3353Ser)
c.5869+3923A>G (n.5869+3923A>G)
2g.21006810T>GCA345987671APOBc.10058A>C (p.Asn3353Thr)
c.5869+3923A>C (n.5869+3923A>C)
ClinVar gnomAD v4
2g.21006811T>ACA345987674APOBc.10057A>T (p.Asn3353Tyr)
c.5869+3922A>T (n.5869+3922A>T)
gnomAD v4
2g.21006811T>CCA345987675APOBc.10057A>G (p.Asn3353Asp)
c.5869+3922A>G (n.5869+3922A>G)
2g.21006811T>GCA042336APOBc.10057A>C (p.Asn3353His)
c.5869+3922A>C (n.5869+3922A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006811T=CA2493474983APOBc.10057A= (p.Asn3353=)
c.5869+3922A= (n.5869+3922A=)
2g.21006812G>ACA042315APOBc.10056C>T (p.Thr3352=)
c.5869+3921C>T (n.5869+3921C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006812G>CCA425343887APOBc.10056C>G (p.Thr3352=)
c.5869+3921C>G (n.5869+3921C>G)
gnomAD v4
2g.21006812G=CA2493474984APOBc.10056C= (p.Thr3352=)
c.5869+3921C= (n.5869+3921C=)
2g.21006812G>TCA042298APOBc.10056C>A (p.Thr3352=)
c.5869+3921C>A (n.5869+3921C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006813G>ACA042281APOBc.10055C>T (p.Thr3352Ile)
c.5869+3920C>T (n.5869+3920C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21006813G>CCA345987682APOBc.10055C>G (p.Thr3352Ser)
c.5869+3920C>G (n.5869+3920C>G)
2g.21006813G=CA2493474985APOBc.10055C= (p.Thr3352=)
c.5869+3920C= (n.5869+3920C=)
2g.21006813G>TCA345987685APOBc.10055C>A (p.Thr3352Asn)
c.5869+3920C>A (n.5869+3920C>A)
2g.21006814T>ACA345987691APOBc.10054A>T (p.Thr3352Ser)
c.5869+3919A>T (n.5869+3919A>T)
2g.21006814T>CCA042262APOBc.10054A>G (p.Thr3352Ala)
c.5869+3919A>G (n.5869+3919A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006814T>GCA345987688APOBc.10054A>C (p.Thr3352Pro)
c.5869+3919A>C (n.5869+3919A>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006814T=CA2493474986APOBc.10054A= (p.Thr3352=)
c.5869+3919A= (n.5869+3919A=)
2g.21006815A>CCA345987693APOBc.10053T>G (p.Asn3351Lys)
c.5869+3918T>G (n.5869+3918T>G)
2g.21006815A>GCA425343889APOBc.10053T>C (p.Asn3351=)
c.5869+3918T>C (n.5869+3918T>C)
ClinVar
2g.21006815A>TCA345987695APOBc.10053T>A (p.Asn3351Lys)
c.5869+3918T>A (n.5869+3918T>A)
gnomAD v4
2g.21006816T>ACA345987698APOBc.10052A>T (p.Asn3351Ile)
c.5869+3917A>T (n.5869+3917A>T)
2g.21006816T>CCA345987700APOBc.10052A>G (p.Asn3351Ser)
c.5869+3917A>G (n.5869+3917A>G)
dbSNP
2g.21006816T>GCA345987702APOBc.10052A>C (p.Asn3351Thr)
c.5869+3917A>C (n.5869+3917A>C)
2g.21006817T>ACA345987708APOBc.10051A>T (p.Asn3351Tyr)
c.5869+3916A>T (n.5869+3916A>T)
2g.21006817T>CCA345987706APOBc.10051A>G (p.Asn3351Asp)
c.5869+3916A>G (n.5869+3916A>G)
ClinVar
2g.21006817T>GCA345987705APOBc.10051A>C (p.Asn3351His)
c.5869+3916A>C (n.5869+3916A>C)
2g.21006818C>ACA425343900APOBc.10050G>T (p.Leu3350=)
c.5869+3915G>T (n.5869+3915G>T)
2g.21006818C>GCA425343901APOBc.10050G>C (p.Leu3350=)
c.5869+3915G>C (n.5869+3915G>C)
2g.21006818C>TCA425343902APOBc.10050G>A (p.Leu3350=)
c.5869+3915G>A (n.5869+3915G>A)
2g.21006819A=CA2493474987APOBc.10049T= (p.Leu3350=)
c.5869+3914T= (n.5869+3914T=)
2g.21006819A>CCA345987711APOBc.10049T>G (p.Leu3350Arg)
c.5869+3914T>G (n.5869+3914T>G)
2g.21006819A>GCA042223APOBc.10049T>C (p.Leu3350Pro)
c.5869+3914T>C (n.5869+3914T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006819A>TCA345987713APOBc.10049T>A (p.Leu3350Gln)
c.5869+3914T>A (n.5869+3914T>A)
dbSNP gnomAD v3 gnomAD v4
2g.21006820G>ACA425343907APOBc.10048C>T (p.Leu3350=)
c.5869+3913C>T (n.5869+3913C>T)
2g.21006820G>CCA345987716APOBc.10048C>G (p.Leu3350Val)
c.5869+3913C>G (n.5869+3913C>G)
2g.21006820G>TCA345987718APOBc.10048C>A (p.Leu3350Met)
c.5869+3913C>A (n.5869+3913C>A)
2g.21006821T>ACA425343912APOBc.10047A>T (p.Thr3349=)
c.5869+3912A>T (n.5869+3912A>T)
gnomAD v4
2g.21006821T>CCA042210APOBc.10047A>G (p.Thr3349=)
c.5869+3912A>G (n.5869+3912A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006821T>GCA425343910APOBc.10047A>C (p.Thr3349=)
c.5869+3912A>C (n.5869+3912A>C)
2g.21006821T=CA2493474988APOBc.10047A= (p.Thr3349=)
c.5869+3912A= (n.5869+3912A=)
2g.21006822G>ACA345987722APOBc.10046C>T (p.Thr3349Ile)
c.5869+3911C>T (n.5869+3911C>T)
2g.21006822G>CCA345987725APOBc.10046C>G (p.Thr3349Arg)
c.5869+3911C>G (n.5869+3911C>G)
2g.21006822G>TCA345987724APOBc.10046C>A (p.Thr3349Lys)
c.5869+3911C>A (n.5869+3911C>A)
2g.21006823T>ACA43496615APOBc.10045A>T (p.Thr3349Ser)
c.5869+3910A>T (n.5869+3910A>T)
dbSNP
2g.21006823T>CCA345987728APOBc.10045A>G (p.Thr3349Ala)
c.5869+3910A>G (n.5869+3910A>G)
2g.21006823T>GCA042196APOBc.10045A>C (p.Thr3349Pro)
c.5869+3910A>C (n.5869+3910A>C)
dbSNP ExAC gnomAD v3 gnomAD v4
2g.21006823T=CA2493474989APOBc.10045A= (p.Thr3349=)
c.5869+3910A= (n.5869+3910A=)
2g.21006824G>ACA425343920APOBc.10044C>T (p.Ile3348=)
c.5869+3909C>T (n.5869+3909C>T)
dbSNP
2g.21006824G>CCA345987732APOBc.10044C>G (p.Ile3348Met)
c.5869+3909C>G (n.5869+3909C>G)
2g.21006824G=CA2493474990APOBc.10044C= (p.Ile3348=)
c.5869+3909C= (n.5869+3909C=)
2g.21006824G>TCA425343918APOBc.10044C>A (p.Ile3348=)
c.5869+3909C>A (n.5869+3909C>A)
2g.21006825A>CCA345987734APOBc.10043T>G (p.Ile3348Ser)
c.5869+3908T>G (n.5869+3908T>G)
2g.21006825A>GCA345987736APOBc.10043T>C (p.Ile3348Thr)
c.5869+3908T>C (n.5869+3908T>C)
gnomAD v4
2g.21006825A>TCA345987737APOBc.10043T>A (p.Ile3348Asn)
c.5869+3908T>A (n.5869+3908T>A)
2g.21006826T>ACA345987739APOBc.10042A>T (p.Ile3348Phe)
c.5869+3907A>T (n.5869+3907A>T)
2g.21006826T>CCA042177APOBc.10042A>G (p.Ile3348Val)
c.5869+3907A>G (n.5869+3907A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006826T>GCA345987743APOBc.10042A>C (p.Ile3348Leu)
c.5869+3907A>C (n.5869+3907A>C)
2g.21006826T=CA2493474991APOBc.10042A= (p.Ile3348=)
c.5869+3907A= (n.5869+3907A=)
2g.21006827G>ACA425343927APOBc.10041C>T (p.Val3347=)
c.5869+3906C>T (n.5869+3906C>T)
2g.21006827G>CCA425343929APOBc.10041C>G (p.Val3347=)
c.5869+3906C>G (n.5869+3906C>G)
2g.21006827G>TCA425343928APOBc.10041C>A (p.Val3347=)
c.5869+3906C>A (n.5869+3906C>A)
2g.21006828A>CCA345987749APOBc.10040T>G (p.Val3347Gly)
c.5869+3905T>G (n.5869+3905T>G)
COSMIC
2g.21006828A>GCA345987747APOBc.10040T>C (p.Val3347Ala)
c.5869+3905T>C (n.5869+3905T>C)
2g.21006828A>TCA345987746APOBc.10040T>A (p.Val3347Asp)
c.5869+3905T>A (n.5869+3905T>A)
2g.21006829C>ACA345987752APOBc.10039G>T (p.Val3347Phe)
c.5869+3904G>T (n.5869+3904G>T)
2g.21006829C>GCA345987755APOBc.10039G>C (p.Val3347Leu)
c.5869+3904G>C (n.5869+3904G>C)
2g.21006829C>TCA345987753APOBc.10039G>A (p.Val3347Ile)
c.5869+3904G>A (n.5869+3904G>A)
2g.21006830A>CCA345987758APOBc.10038T>G (p.Ser3346Arg)
c.5869+3903T>G (n.5869+3903T>G)
2g.21006830A>GCA425343934APOBc.10038T>C (p.Ser3346=)
c.5869+3903T>C (n.5869+3903T>C)
2g.21006830A>TCA345987759APOBc.10038T>A (p.Ser3346Arg)
c.5869+3903T>A (n.5869+3903T>A)

Number of alleles fetched