Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21006526T>ACA345986736APOBc.10342A>T (p.Thr3448Ser)
c.5869+4207A>T (n.5869+4207A>T)
dbSNP gnomAD v3 gnomAD v4
2g.21006526T>CCA345986737APOBc.10342A>G (p.Thr3448Ala)
c.5869+4207A>G (n.5869+4207A>G)
2g.21006526T>GCA345986738APOBc.10342A>C (p.Thr3448Pro)
c.5869+4207A>C (n.5869+4207A>C)
2g.21006526T=CA2493474830APOBc.10342A= (p.Thr3448=)
c.5869+4207A= (n.5869+4207A=)
2g.21006527A=CA2493474831APOBc.10341T= (p.Asn3447=)
c.5869+4206T= (n.5869+4206T=)
2g.21006527A>CCA345986739APOBc.10341T>G (p.Asn3447Lys)
c.5869+4206T>G (n.5869+4206T>G)
2g.21006527A>GCA425343276APOBc.10341T>C (p.Asn3447=)
c.5869+4206T>C (n.5869+4206T>C)
2g.21006527A>TCA345986740APOBc.10341T>A (p.Asn3447Lys)
c.5869+4206T>A (n.5869+4206T>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006528T>ACA345986743APOBc.10340A>T (p.Asn3447Ile)
c.5869+4205A>T (n.5869+4205A>T)
2g.21006528T>CCA345986742APOBc.10340A>G (p.Asn3447Ser)
c.5869+4205A>G (n.5869+4205A>G)
2g.21006528T>GCA345986741APOBc.10340A>C (p.Asn3447Thr)
c.5869+4205A>C (n.5869+4205A>C)
2g.21006529T>ACA345986744APOBc.10339A>T (p.Asn3447Tyr)
c.5869+4204A>T (n.5869+4204A>T)
2g.21006529T>CCA345986745APOBc.10339A>G (p.Asn3447Asp)
c.5869+4204A>G (n.5869+4204A>G)
2g.21006529T>GCA345986746APOBc.10339A>C (p.Asn3447His)
c.5869+4204A>C (n.5869+4204A>C)
2g.21006530T>ACA425343284APOBc.10338A>T (p.Gly3446=)
c.5869+4203A>T (n.5869+4203A>T)
2g.21006530T>CCA425343285APOBc.10338A>G (p.Gly3446=)
c.5869+4203A>G (n.5869+4203A>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006530T>GCA425343286APOBc.10338A>C (p.Gly3446=)
c.5869+4203A>C (n.5869+4203A>C)
2g.21006530T=CA2493474832APOBc.10338A= (p.Gly3446=)
c.5869+4203A= (n.5869+4203A=)
2g.21006531C>ACA345986747APOBc.10337G>T (p.Gly3446Val)
c.5869+4202G>T (n.5869+4202G>T)
2g.21006531C>GCA345986748APOBc.10337G>C (p.Gly3446Ala)
c.5869+4202G>C (n.5869+4202G>C)
2g.21006531C>TCA345986749APOBc.10337G>A (p.Gly3446Glu)
c.5869+4202G>A (n.5869+4202G>A)
COSMIC
2g.21006532C>ACA345986752APOBc.10336G>T (p.Gly3446Ter)
c.5869+4201G>T (n.5869+4201G>T)
2g.21006532C=CA2493474833APOBc.10336G= (p.Gly3446=)
c.5869+4201G= (n.5869+4201G=)
2g.21006532C>GCA345986751APOBc.10336G>C (p.Gly3446Arg)
c.5869+4201G>C (n.5869+4201G>C)
2g.21006532C>TCA345986750APOBc.10336G>A (p.Gly3446Arg)
c.5869+4201G>A (n.5869+4201G>A)
dbSNP gnomAD v3 gnomAD v4
2g.21006533A=CA2493474834APOBc.10335T= (p.Asn3445=)
c.5869+4200T= (n.5869+4200T=)
2g.21006533A>CCA345986753APOBc.10335T>G (p.Asn3445Lys)
c.5869+4200T>G (n.5869+4200T>G)
gnomAD v4
2g.21006533A>GCA425343290APOBc.10335T>C (p.Asn3445=)
c.5869+4200T>C (n.5869+4200T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006533A>TCA345986754APOBc.10335T>A (p.Asn3445Lys)
c.5869+4200T>A (n.5869+4200T>A)
2g.21006534T>ACA345986755APOBc.10334A>T (p.Asn3445Ile)
c.5869+4199A>T (n.5869+4199A>T)
2g.21006534T>CCA345986757APOBc.10334A>G (p.Asn3445Ser)
c.5869+4199A>G (n.5869+4199A>G)
2g.21006534T>GCA345986756APOBc.10334A>C (p.Asn3445Thr)
c.5869+4199A>C (n.5869+4199A>C)
dbSNP
2g.21006534T=CA2493474835APOBc.10334A= (p.Asn3445=)
c.5869+4199A= (n.5869+4199A=)
2g.21006535T>ACA345986758APOBc.10333A>T (p.Asn3445Tyr)
c.5869+4198A>T (n.5869+4198A>T)
2g.21006535T>CCA043220APOBc.10333A>G (p.Asn3445Asp)
c.5869+4198A>G (n.5869+4198A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006535T>GCA345986759APOBc.10333A>C (p.Asn3445His)
c.5869+4198A>C (n.5869+4198A>C)
2g.21006535T=CA2493474836APOBc.10333A= (p.Asn3445=)
c.5869+4198A= (n.5869+4198A=)
2g.21006536A=CA2493474837APOBc.10332T= (p.Leu3444=)
c.5869+4197T= (n.5869+4197T=)
2g.21006536A>CCA43495995APOBc.10332T>G (p.Leu3444=)
c.5869+4197T>G (n.5869+4197T>G)
dbSNP
2g.21006536A>GCA043199APOBc.10332T>C (p.Leu3444=)
c.5869+4197T>C (n.5869+4197T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006536A>TCA425343298APOBc.10332T>A (p.Leu3444=)
c.5869+4197T>A (n.5869+4197T>A)
2g.21006537A=CA2493474838APOBc.10331T= (p.Leu3444=)
c.5869+4196T= (n.5869+4196T=)
2g.21006537A>CCA345986761APOBc.10331T>G (p.Leu3444Arg)
c.5869+4196T>G (n.5869+4196T>G)
2g.21006537A>GCA345986760APOBc.10331T>C (p.Leu3444Pro)
c.5869+4196T>C (n.5869+4196T>C)
COSMIC
2g.21006537A>TCA345986762APOBc.10331T>A (p.Leu3444His)
c.5869+4196T>A (n.5869+4196T>A)
ClinVar dbSNP gnomAD v4
2g.21006538G>ACA345986763APOBc.10330C>T (p.Leu3444Phe)
c.5869+4195C>T (n.5869+4195C>T)
2g.21006538G>CCA345986765APOBc.10330C>G (p.Leu3444Val)
c.5869+4195C>G (n.5869+4195C>G)
gnomAD v4
2g.21006538G=CA2493474839APOBc.10330C= (p.Leu3444=)
c.5869+4195C= (n.5869+4195C=)
2g.21006538G>TCA345986764APOBc.10330C>A (p.Leu3444Ile)
c.5869+4195C>A (n.5869+4195C>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006539T>ACA345986766APOBc.10329A>T (p.Glu3443Asp)
c.5869+4194A>T (n.5869+4194A>T)
2g.21006539T>CCA425343302APOBc.10329A>G (p.Glu3443=)
c.5869+4194A>G (n.5869+4194A>G)
2g.21006539T>GCA345986767APOBc.10329A>C (p.Glu3443Asp)
c.5869+4194A>C (n.5869+4194A>C)
2g.21006540T>ACA345986768APOBc.10328A>T (p.Glu3443Val)
c.5869+4193A>T (n.5869+4193A>T)
2g.21006540T>CCA345986769APOBc.10328A>G (p.Glu3443Gly)
c.5869+4193A>G (n.5869+4193A>G)
2g.21006540T>GCA345986770APOBc.10328A>C (p.Glu3443Ala)
c.5869+4193A>C (n.5869+4193A>C)
2g.21006541C>ACA345986771APOBc.10327G>T (p.Glu3443Ter)
c.5869+4192G>T (n.5869+4192G>T)
ClinVar dbSNP gnomAD v4
2g.21006541C>GCA345986772APOBc.10327G>C (p.Glu3443Gln)
c.5869+4192G>C (n.5869+4192G>C)
2g.21006541C>TCA345986773APOBc.10327G>A (p.Glu3443Lys)
c.5869+4192G>A (n.5869+4192G>A)
gnomAD v4
2g.21006542T>ACA345986774APOBc.10326A>T (p.Gln3442His)
c.5869+4191A>T (n.5869+4191A>T)
2g.21006542T>CCA043188APOBc.10326A>G (p.Gln3442=)
c.5869+4191A>G (n.5869+4191A>G)
ClinVar dbSNP ExAC gnomAD v4
2g.21006542T>GCA345986775APOBc.10326A>C (p.Gln3442His)
c.5869+4191A>C (n.5869+4191A>C)
COSMIC
2g.21006542T=CA2493474840APOBc.10326A= (p.Gln3442=)
c.5869+4191A= (n.5869+4191A=)
2g.21006543T>ACA345986778APOBc.10325A>T (p.Gln3442Leu)
c.5869+4190A>T (n.5869+4190A>T)
2g.21006543T>CCA345986776APOBc.10325A>G (p.Gln3442Arg)
c.5869+4190A>G (n.5869+4190A>G)
2g.21006543T>GCA345986777APOBc.10325A>C (p.Gln3442Pro)
c.5869+4190A>C (n.5869+4190A>C)
2g.21006544G>ACA345986779APOBc.10324C>T (p.Gln3442Ter)
c.5869+4189C>T (n.5869+4189C>T)
2g.21006544G>CCA345986780APOBc.10324C>G (p.Gln3442Glu)
c.5869+4189C>G (n.5869+4189C>G)
2g.21006544G=CA2493474841APOBc.10324C= (p.Gln3442=)
c.5869+4189C= (n.5869+4189C=)
2g.21006544G>TCA345986781APOBc.10324C>A (p.Gln3442Lys)
c.5869+4189C>A (n.5869+4189C>A)
ClinVar dbSNP gnomAD v4
2g.21006545C>ACA345986782APOBc.10323G>T (p.Lys3441Asn)
c.5869+4188G>T (n.5869+4188G>T)
2g.21006545C=CA2493474842APOBc.10323G= (p.Lys3441=)
c.5869+4188G= (n.5869+4188G=)
2g.21006545C>GCA345986783APOBc.10323G>C (p.Lys3441Asn)
c.5869+4188G>C (n.5869+4188G>C)
2g.21006545C>TCA425343307APOBc.10323G>A (p.Lys3441=)
c.5869+4188G>A (n.5869+4188G>A)
ClinVar dbSNP
2g.21006546T>ACA345986784APOBc.10322A>T (p.Lys3441Met)
c.5869+4187A>T (n.5869+4187A>T)
2g.21006546T>CCA345986785APOBc.10322A>G (p.Lys3441Arg)
c.5869+4187A>G (n.5869+4187A>G)
2g.21006546T>GCA345986786APOBc.10322A>C (p.Lys3441Thr)
c.5869+4187A>C (n.5869+4187A>C)
2g.21006547T>ACA345986787APOBc.10321A>T (p.Lys3441Ter)
c.5869+4186A>T (n.5869+4186A>T)
2g.21006547T>CCA345986788APOBc.10321A>G (p.Lys3441Glu)
c.5869+4186A>G (n.5869+4186A>G)
2g.21006547T>GCA345986789APOBc.10321A>C (p.Lys3441Gln)
c.5869+4186A>C (n.5869+4186A>C)
2g.21006548G>ACA043171APOBc.10320C>T (p.Phe3440=)
c.5869+4185C>T (n.5869+4185C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21006548G>CCA345986791APOBc.10320C>G (p.Phe3440Leu)
c.5869+4185C>G (n.5869+4185C>G)
2g.21006548G=CA2493474843APOBc.10320C= (p.Phe3440=)
c.5869+4185C= (n.5869+4185C=)
2g.21006548G>TCA345986790APOBc.10320C>A (p.Phe3440Leu)
c.5869+4185C>A (n.5869+4185C>A)
2g.21006549A>CCA345986792APOBc.10319T>G (p.Phe3440Cys)
c.5869+4184T>G (n.5869+4184T>G)
2g.21006549A>GCA345986793APOBc.10319T>C (p.Phe3440Ser)
c.5869+4184T>C (n.5869+4184T>C)
2g.21006549A>TCA345986794APOBc.10319T>A (p.Phe3440Tyr)
c.5869+4184T>A (n.5869+4184T>A)
2g.21006550A=CA2493474844APOBc.10318T= (p.Phe3440=)
c.5869+4183T= (n.5869+4183T=)
2g.21006550A>CCA43496047APOBc.10318T>G (p.Phe3440Val)
c.5869+4183T>G (n.5869+4183T>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21006550A>GCA345986795APOBc.10318T>C (p.Phe3440Leu)
c.5869+4183T>C (n.5869+4183T>C)
2g.21006550A>TCA345986796APOBc.10318T>A (p.Phe3440Ile)
c.5869+4183T>A (n.5869+4183T>A)
2g.21006551A=CA2493474845APOBc.10317T= (p.Asn3439=)
c.5869+4182T= (n.5869+4182T=)
2g.21006551A>CCA345986798APOBc.10317T>G (p.Asn3439Lys)
c.5869+4182T>G (n.5869+4182T>G)
2g.21006551A>GCA425343321APOBc.10317T>C (p.Asn3439=)
c.5869+4182T>C (n.5869+4182T>C)
ClinVar dbSNP
2g.21006551A>TCA345986797APOBc.10317T>A (p.Asn3439Lys)
c.5869+4182T>A (n.5869+4182T>A)
2g.21006552T>ACA345986799APOBc.10316A>T (p.Asn3439Ile)
c.5869+4181A>T (n.5869+4181A>T)
2g.21006552T>CCA345986800APOBc.10316A>G (p.Asn3439Ser)
c.5869+4181A>G (n.5869+4181A>G)
2g.21006552T>GCA345986801APOBc.10316A>C (p.Asn3439Thr)
c.5869+4181A>C (n.5869+4181A>C)
2g.21006553T>ACA345986802APOBc.10315A>T (p.Asn3439Tyr)
c.5869+4180A>T (n.5869+4180A>T)
dbSNP gnomAD v2 gnomAD v4
2g.21006553T>CCA345986803APOBc.10315A>G (p.Asn3439Asp)
c.5869+4180A>G (n.5869+4180A>G)
dbSNP
2g.21006553T>GCA345986804APOBc.10315A>C (p.Asn3439His)
c.5869+4180A>C (n.5869+4180A>C)
2g.21006553T=CA2493474846APOBc.10315A= (p.Asn3439=)
c.5869+4180A= (n.5869+4180A=)
2g.21006554C>ACA43496054APOBc.10314G>T (p.Met3438Ile)
c.5869+4179G>T (n.5869+4179G>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21006554C=CA2493474847APOBc.10314G= (p.Met3438=)
c.5869+4179G= (n.5869+4179G=)
2g.21006554C>GCA345986806APOBc.10314G>C (p.Met3438Ile)
c.5869+4179G>C (n.5869+4179G>C)
2g.21006554C>TCA345986805APOBc.10314G>A (p.Met3438Ile)
c.5869+4179G>A (n.5869+4179G>A)
2g.21006554_21006563delinsCATTCTCAAACA2493474848APOBc.10305_10314delinsTTTGAGAATG (p.Ile3435=)
c.5869+4170_5869+4179delinsTTTGAGAATG (n.5869+4170_5869+4179delinsTTTGAGAATG)
2g.21006555A>CCA345986807APOBc.10313T>G (p.Met3438Arg)
c.5869+4178T>G (n.5869+4178T>G)
2g.21006555A>GCA345986808APOBc.10313T>C (p.Met3438Thr)
c.5869+4178T>C (n.5869+4178T>C)
2g.21006555A>TCA345986809APOBc.10313T>A (p.Met3438Lys)
c.5869+4178T>A (n.5869+4178T>A)
2g.21006558_21006566delCA916487986APOBc.10305_10313del (p.Ile3435_Arg3437del)
c.5869+4170_5869+4178del (n.5869+4170_5869+4178del)
dbSNP
2g.21006556T>ACA345986810APOBc.10312A>T (p.Met3438Leu)
c.5869+4177A>T (n.5869+4177A>T)
2g.21006556T>CCA345986811APOBc.10312A>G (p.Met3438Val)
c.5869+4177A>G (n.5869+4177A>G)
dbSNP gnomAD v3 gnomAD v4
2g.21006556T>GCA345986812APOBc.10312A>C (p.Met3438Leu)
c.5869+4177A>C (n.5869+4177A>C)
2g.21006556T=CA2493474849APOBc.10312A= (p.Met3438=)
c.5869+4177A= (n.5869+4177A=)
2g.21006557delCA2586968761APOBc.10312del (p.Met3438Ter)
c.5869+4177del (n.5869+4177del)
gnomAD v4
2g.21006557T>ACA345986813APOBc.10311A>T (p.Arg3437Ser)
c.5869+4176A>T (n.5869+4176A>T)
2g.21006557T>CCA425343332APOBc.10311A>G (p.Arg3437=)
c.5869+4176A>G (n.5869+4176A>G)
2g.21006557T>GCA345986814APOBc.10311A>C (p.Arg3437Ser)
c.5869+4176A>C (n.5869+4176A>C)
2g.21006558C>ACA345986815APOBc.10310G>T (p.Arg3437Ile)
c.5869+4175G>T (n.5869+4175G>T)
2g.21006558C=CA2493474850APOBc.10310G= (p.Arg3437=)
c.5869+4175G= (n.5869+4175G=)
2g.21006558C>GCA345986816APOBc.10310G>C (p.Arg3437Thr)
c.5869+4175G>C (n.5869+4175G>C)
2g.21006558C>TCA345986817APOBc.10310G>A (p.Arg3437Lys)
c.5869+4175G>A (n.5869+4175G>A)
ClinVar dbSNP
2g.21006559T>ACA345986819APOBc.10309A>T (p.Arg3437Ter)
c.5869+4174A>T (n.5869+4174A>T)
2g.21006559T>CCA345986820APOBc.10309A>G (p.Arg3437Gly)
c.5869+4174A>G (n.5869+4174A>G)
2g.21006559T>GCA425343335APOBc.10309A>C (p.Arg3437=)
c.5869+4174A>C (n.5869+4174A>C)
2g.21006560C>ACA345986821APOBc.10308G>T (p.Leu3436Phe)
c.5869+4173G>T (n.5869+4173G>T)
2g.21006560C>GCA345986822APOBc.10308G>C (p.Leu3436Phe)
c.5869+4173G>C (n.5869+4173G>C)
gnomAD v4
2g.21006560C>TCA425343339APOBc.10308G>A (p.Leu3436=)
c.5869+4173G>A (n.5869+4173G>A)
2g.21006561A>CCA345986823APOBc.10307T>G (p.Leu3436Trp)
c.5869+4172T>G (n.5869+4172T>G)
2g.21006561A>GCA345986825APOBc.10307T>C (p.Leu3436Ser)
c.5869+4172T>C (n.5869+4172T>C)
2g.21006561A>TCA345986824APOBc.10307T>A (p.Leu3436Ter)
c.5869+4172T>A (n.5869+4172T>A)
gnomAD v4
2g.21006562A=CA2493474851APOBc.10306T= (p.Leu3436=)
c.5869+4171T= (n.5869+4171T=)
2g.21006562A>CCA345986826APOBc.10306T>G (p.Leu3436Val)
c.5869+4171T>G (n.5869+4171T>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21006562A>GCA043158APOBc.10306T>C (p.Leu3436=)
c.5869+4171T>C (n.5869+4171T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006562A>TCA345986827APOBc.10306T>A (p.Leu3436Met)
c.5869+4171T>A (n.5869+4171T>A)
2g.21006563A>CCA345986828APOBc.10305T>G (p.Ile3435Met)
c.5869+4170T>G (n.5869+4170T>G)
2g.21006563A>GCA425343344APOBc.10305T>C (p.Ile3435=)
c.5869+4170T>C (n.5869+4170T>C)
2g.21006563A>TCA425343345APOBc.10305T>A (p.Ile3435=)
c.5869+4170T>A (n.5869+4170T>A)
2g.21006564A=CA2493474852APOBc.10304T= (p.Ile3435=)
c.5869+4169T= (n.5869+4169T=)
2g.21006564A>CCA345986829APOBc.10304T>G (p.Ile3435Ser)
c.5869+4169T>G (n.5869+4169T>G)
2g.21006564A>GCA043140APOBc.10304T>C (p.Ile3435Thr)
c.5869+4169T>C (n.5869+4169T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006564A>TCA345986830APOBc.10304T>A (p.Ile3435Asn)
c.5869+4169T>A (n.5869+4169T>A)
ClinVar
2g.21006565T>ACA345986831APOBc.10303A>T (p.Ile3435Phe)
c.5869+4168A>T (n.5869+4168A>T)
2g.21006565T>CCA345986832APOBc.10303A>G (p.Ile3435Val)
c.5869+4168A>G (n.5869+4168A>G)
2g.21006565T>GCA345986833APOBc.10303A>C (p.Ile3435Leu)
c.5869+4168A>C (n.5869+4168A>C)
2g.21006566T>ACA425343349APOBc.10302A>T (p.Pro3434=)
c.5869+4167A>T (n.5869+4167A>T)
2g.21006566T>CCA425343351APOBc.10302A>G (p.Pro3434=)
c.5869+4167A>G (n.5869+4167A>G)
2g.21006566T>GCA425343350APOBc.10302A>C (p.Pro3434=)
c.5869+4167A>C (n.5869+4167A>C)
2g.21006567G>ACA345986836APOBc.10301C>T (p.Pro3434Leu)
c.5869+4166C>T (n.5869+4166C>T)
gnomAD v4
2g.21006567G>CCA345986835APOBc.10301C>G (p.Pro3434Arg)
c.5869+4166C>G (n.5869+4166C>G)
2g.21006567G=CA2493474853APOBc.10301C= (p.Pro3434=)
c.5869+4166C= (n.5869+4166C=)
2g.21006567G>TCA345986834APOBc.10301C>A (p.Pro3434Gln)
c.5869+4166C>A (n.5869+4166C>A)
2g.21006567_21006568insACA916487987APOBc.10300_10301insT (p.Pro3434LeufsTer12)
c.5869+4165_5869+4166insT (n.5869+4165_5869+4166insT)
dbSNP
2g.21006568G>ACA345986837APOBc.10300C>T (p.Pro3434Ser)
c.5869+4165C>T (n.5869+4165C>T)
2g.21006568G>CCA345986838APOBc.10300C>G (p.Pro3434Ala)
c.5869+4165C>G (n.5869+4165C>G)
2g.21006568G>TCA345986839APOBc.10300C>A (p.Pro3434Thr)
c.5869+4165C>A (n.5869+4165C>A)
2g.21006569A>CCA345986840APOBc.10299T>G (p.Ile3433Met)
c.5869+4164T>G (n.5869+4164T>G)
2g.21006569A>GCA425343354APOBc.10299T>C (p.Ile3433=)
c.5869+4164T>C (n.5869+4164T>C)
2g.21006569A>TCA425343355APOBc.10299T>A (p.Ile3433=)
c.5869+4164T>A (n.5869+4164T>A)
2g.21006570A>CCA345986841APOBc.10298T>G (p.Ile3433Ser)
c.5869+4163T>G (n.5869+4163T>G)
2g.21006570A>GCA345986842APOBc.10298T>C (p.Ile3433Thr)
c.5869+4163T>C (n.5869+4163T>C)
2g.21006570A>TCA345986843APOBc.10298T>A (p.Ile3433Asn)
c.5869+4163T>A (n.5869+4163T>A)
2g.21006571T>ACA345986844APOBc.10297A>T (p.Ile3433Phe)
c.5869+4162A>T (n.5869+4162A>T)
2g.21006571T>CCA345986845APOBc.10297A>G (p.Ile3433Val)
c.5869+4162A>G (n.5869+4162A>G)
2g.21006571T>GCA345986846APOBc.10297A>C (p.Ile3433Leu)
c.5869+4162A>C (n.5869+4162A>C)
2g.21006572T>ACA345986847APOBc.10296A>T (p.Gln3432His)
c.5869+4161A>T (n.5869+4161A>T)
dbSNP
2g.21006572T>CCA425343360APOBc.10296A>G (p.Gln3432=)
c.5869+4161A>G (n.5869+4161A>G)
2g.21006572T>GCA345986848APOBc.10296A>C (p.Gln3432His)
c.5869+4161A>C (n.5869+4161A>C)
2g.21006572T=CA2493474854APOBc.10296A= (p.Gln3432=)
c.5869+4161A= (n.5869+4161A=)
2g.21006573T>ACA345986850APOBc.10295A>T (p.Gln3432Leu)
c.5869+4160A>T (n.5869+4160A>T)
2g.21006573T>CCA043118APOBc.10295A>G (p.Gln3432Arg)
c.5869+4160A>G (n.5869+4160A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006573T>GCA345986849APOBc.10295A>C (p.Gln3432Pro)
c.5869+4160A>C (n.5869+4160A>C)
gnomAD v4
2g.21006573T=CA2493474855APOBc.10295A= (p.Gln3432=)
c.5869+4160A= (n.5869+4160A=)
2g.21006574G>ACA345986851APOBc.10294C>T (p.Gln3432Ter)
c.5869+4159C>T (n.5869+4159C>T)
2g.21006574G>CCA022744APOBc.10294C>G (p.Gln3432Glu)
c.5869+4159C>G (n.5869+4159C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006574G=CA2493474856APOBc.10294C= (p.Gln3432=)
c.5869+4159C= (n.5869+4159C=)
2g.21006574G>TCA345986852APOBc.10294C>A (p.Gln3432Lys)
c.5869+4159C>A (n.5869+4159C>A)
2g.21006575G>ACA425343363APOBc.10293C>T (p.Ala3431=)
c.5869+4158C>T (n.5869+4158C>T)
ClinVar gnomAD v4
2g.21006575G>CCA425343364APOBc.10293C>G (p.Ala3431=)
c.5869+4158C>G (n.5869+4158C>G)
gnomAD v4
2g.21006575G=CA2493474857APOBc.10293C= (p.Ala3431=)
c.5869+4158C= (n.5869+4158C=)
2g.21006575G>TCA425343365APOBc.10293C>A (p.Ala3431=)
c.5869+4158C>A (n.5869+4158C>A)
gnomAD v3 gnomAD v4
2g.21006576G>ACA345986853APOBc.10292C>T (p.Ala3431Val)
c.5869+4157C>T (n.5869+4157C>T)
gnomAD v4
2g.21006576G>CCA345986854APOBc.10292C>G (p.Ala3431Gly)
c.5869+4157C>G (n.5869+4157C>G)
2g.21006576G>TCA345986855APOBc.10292C>A (p.Ala3431Asp)
c.5869+4157C>A (n.5869+4157C>A)
ClinVar dbSNP
2g.21006576_21006577insAGCA916487988APOBc.10292_10293insTC (p.Gln3432ProfsTer6)
c.5869+4157_5869+4158insTC (n.5869+4157_5869+4158insTC)
dbSNP
2g.21006577C>ACA345986858APOBc.10291G>T (p.Ala3431Ser)
c.5869+4156G>T (n.5869+4156G>T)
2g.21006577C>GCA345986856APOBc.10291G>C (p.Ala3431Pro)
c.5869+4156G>C (n.5869+4156G>C)
gnomAD v4
2g.21006577C>TCA345986857APOBc.10291G>A (p.Ala3431Thr)
c.5869+4156G>A (n.5869+4156G>A)
2g.21006578T>ACA345986859APOBc.10290A>T (p.Lys3430Asn)
c.5869+4155A>T (n.5869+4155A>T)
dbSNP
2g.21006578T>CCA425343368APOBc.10290A>G (p.Lys3430=)
c.5869+4155A>G (n.5869+4155A>G)
2g.21006578T>GCA345986860APOBc.10290A>C (p.Lys3430Asn)
c.5869+4155A>C (n.5869+4155A>C)
2g.21006578T=CA2493474858APOBc.10290A= (p.Lys3430=)
c.5869+4155A= (n.5869+4155A=)
2g.21006579T>ACA345986861APOBc.10289A>T (p.Lys3430Ile)
c.5869+4154A>T (n.5869+4154A>T)
2g.21006579T>CCA345986862APOBc.10289A>G (p.Lys3430Arg)
c.5869+4154A>G (n.5869+4154A>G)
2g.21006579T>GCA043058APOBc.10289A>C (p.Lys3430Thr)
c.5869+4154A>C (n.5869+4154A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006579T=CA2493474859APOBc.10289A= (p.Lys3430=)
c.5869+4154A= (n.5869+4154A=)
2g.21006579_21006580insGGAGGCA916487990APOBc.10288_10289insCCTCC (p.Lys3430ThrfsTer9)
c.5869+4153_5869+4154insCCTCC (n.5869+4153_5869+4154insCCTCC)
dbSNP
2g.21006580T>ACA345986863APOBc.10288A>T (p.Lys3430Ter)
c.5869+4153A>T (n.5869+4153A>T)
2g.21006580T>CCA043029APOBc.10288A>G (p.Lys3430Glu)
c.5869+4153A>G (n.5869+4153A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006580T>GCA345986864APOBc.10288A>C (p.Lys3430Gln)
c.5869+4153A>C (n.5869+4153A>C)
2g.21006580T=CA2493474860APOBc.10288A= (p.Lys3430=)
c.5869+4153A= (n.5869+4153A=)
2g.21006581T>ACA425343374APOBc.10287A>T (p.Thr3429=)
c.5869+4152A>T (n.5869+4152A>T)
2g.21006581T>CCA425343371APOBc.10287A>G (p.Thr3429=)
c.5869+4152A>G (n.5869+4152A>G)
2g.21006581T>GCA425343372APOBc.10287A>C (p.Thr3429=)
c.5869+4152A>C (n.5869+4152A>C)
2g.21006582G>ACA345986865APOBc.10286C>T (p.Thr3429Ile)
c.5869+4151C>T (n.5869+4151C>T)
2g.21006582G>CCA345986866APOBc.10286C>G (p.Thr3429Arg)
c.5869+4151C>G (n.5869+4151C>G)
ClinVar
2g.21006582G>TCA345986867APOBc.10286C>A (p.Thr3429Lys)
c.5869+4151C>A (n.5869+4151C>A)
2g.21006582_21006583delinsGTCA2493474861APOBc.10285_10286delinsAC (p.Thr3429=)
c.5869+4150_5869+4151delinsAC (n.5869+4150_5869+4151delinsAC)
2g.21006583delCA916487991APOBc.10285del (p.Thr3429GlnfsTer8)
c.5869+4150del (n.5869+4150del)
dbSNP
2g.21006583T>ACA345986868APOBc.10285A>T (p.Thr3429Ser)
c.5869+4150A>T (n.5869+4150A>T)
2g.21006583T>CCA345986869APOBc.10285A>G (p.Thr3429Ala)
c.5869+4150A>G (n.5869+4150A>G)
dbSNP
2g.21006583T>GCA345986870APOBc.10285A>C (p.Thr3429Pro)
c.5869+4150A>C (n.5869+4150A>C)
2g.21006584G>ACA425343376APOBc.10284C>T (p.Thr3428=)
c.5869+4149C>T (n.5869+4149C>T)
2g.21006584G>CCA425343377APOBc.10284C>G (p.Thr3428=)
c.5869+4149C>G (n.5869+4149C>G)
2g.21006584G=CA2493474862APOBc.10284C= (p.Thr3428=)
c.5869+4149C= (n.5869+4149C=)
2g.21006584G>TCA425343378APOBc.10284C>A (p.Thr3428=)
c.5869+4149C>A (n.5869+4149C>A)
2g.21006584_21006585insCACA916487992APOBc.10283_10284insTG (p.Thr3429AlafsTer9)
c.5869+4148_5869+4149insTG (n.5869+4148_5869+4149insTG)
dbSNP
2g.21006585G>ACA345986871APOBc.10283C>T (p.Thr3428Ile)
c.5869+4148C>T (n.5869+4148C>T)
dbSNP gnomAD v2 gnomAD v4
2g.21006585G>CCA345986872APOBc.10283C>G (p.Thr3428Ser)
c.5869+4148C>G (n.5869+4148C>G)
2g.21006585G=CA2493474863APOBc.10283C= (p.Thr3428=)
c.5869+4148C= (n.5869+4148C=)
2g.21006585G>TCA043011APOBc.10283C>A (p.Thr3428Asn)
c.5869+4148C>A (n.5869+4148C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006586T>ACA345986873APOBc.10282A>T (p.Thr3428Ser)
c.5869+4147A>T (n.5869+4147A>T)
dbSNP
2g.21006586T>CCA345986874APOBc.10282A>G (p.Thr3428Ala)
c.5869+4147A>G (n.5869+4147A>G)
2g.21006586T>GCA345986875APOBc.10282A>C (p.Thr3428Pro)
c.5869+4147A>C (n.5869+4147A>C)
2g.21006586T=CA2493474864APOBc.10282A= (p.Thr3428=)
c.5869+4147A= (n.5869+4147A=)
2g.21006587T>ACA425343381APOBc.10281A>T (p.Thr3427=)
c.5869+4146A>T (n.5869+4146A>T)
2g.21006587T>CCA425343383APOBc.10281A>G (p.Thr3427=)
c.5869+4146A>G (n.5869+4146A>G)
2g.21006587T>GCA425343382APOBc.10281A>C (p.Thr3427=)
c.5869+4146A>C (n.5869+4146A>C)
2g.21006588G>ACA345986876APOBc.10280C>T (p.Thr3427Ile)
c.5869+4145C>T (n.5869+4145C>T)
2g.21006588G>CCA345986877APOBc.10280C>G (p.Thr3427Arg)
c.5869+4145C>G (n.5869+4145C>G)
2g.21006588G=CA2493474865APOBc.10280C= (p.Thr3427=)
c.5869+4145C= (n.5869+4145C=)
2g.21006588G>TCA43496136APOBc.10280C>A (p.Thr3427Lys)
c.5869+4145C>A (n.5869+4145C>A)
dbSNP
2g.21006589T>ACA345986878APOBc.10279A>T (p.Thr3427Ser)
c.5869+4144A>T (n.5869+4144A>T)
2g.21006589T>CCA345986880APOBc.10279A>G (p.Thr3427Ala)
c.5869+4144A>G (n.5869+4144A>G)
2g.21006589T>GCA345986879APOBc.10279A>C (p.Thr3427Pro)
c.5869+4144A>C (n.5869+4144A>C)
2g.21006590T>ACA425343390APOBc.10278A>T (p.Ala3426=)
c.5869+4143A>T (n.5869+4143A>T)
2g.21006590T>CCA425343391APOBc.10278A>G (p.Ala3426=)
c.5869+4143A>G (n.5869+4143A>G)
2g.21006590T>GCA425343394APOBc.10278A>C (p.Ala3426=)
c.5869+4143A>C (n.5869+4143A>C)
2g.21006591G>ACA345986881APOBc.10277C>T (p.Ala3426Val)
c.5869+4142C>T (n.5869+4142C>T)
2g.21006591G>CCA345986882APOBc.10277C>G (p.Ala3426Gly)
c.5869+4142C>G (n.5869+4142C>G)
dbSNP
2g.21006591G=CA2493474866APOBc.10277C= (p.Ala3426=)
c.5869+4142C= (n.5869+4142C=)
2g.21006591G>TCA43496140APOBc.10277C>A (p.Ala3426Glu)
c.5869+4142C>A (n.5869+4142C>A)
dbSNP
2g.21006592C>ACA345986883APOBc.10276G>T (p.Ala3426Ser)
c.5869+4141G>T (n.5869+4141G>T)
2g.21006592C=CA2493474867APOBc.10276G= (p.Ala3426=)
c.5869+4141G= (n.5869+4141G=)
2g.21006592C>GCA345986884APOBc.10276G>C (p.Ala3426Pro)
c.5869+4141G>C (n.5869+4141G>C)
2g.21006592C>TCA042985APOBc.10276G>A (p.Ala3426Thr)
c.5869+4141G>A (n.5869+4141G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006593C>ACA425343396APOBc.10275G>T (p.Val3425=)
c.5869+4140G>T (n.5869+4140G>T)
gnomAD v4
2g.21006593C>GCA425343398APOBc.10275G>C (p.Val3425=)
c.5869+4140G>C (n.5869+4140G>C)
2g.21006593C>TCA425343397APOBc.10275G>A (p.Val3425=)
c.5869+4140G>A (n.5869+4140G>A)
2g.21006594A>CCA345986885APOBc.10274T>G (p.Val3425Gly)
c.5869+4139T>G (n.5869+4139T>G)
2g.21006594A>GCA345986886APOBc.10274T>C (p.Val3425Ala)
c.5869+4139T>C (n.5869+4139T>C)
gnomAD v4
2g.21006594A>TCA345986887APOBc.10274T>A (p.Val3425Glu)
c.5869+4139T>A (n.5869+4139T>A)
2g.21006595C>ACA345986888APOBc.10273G>T (p.Val3425Leu)
c.5869+4138G>T (n.5869+4138G>T)
2g.21006595C>GCA345986889APOBc.10273G>C (p.Val3425Leu)
c.5869+4138G>C (n.5869+4138G>C)
2g.21006595C>TCA345986890APOBc.10273G>A (p.Val3425Met)
c.5869+4138G>A (n.5869+4138G>A)
2g.21006596T>ACA425343494APOBc.10272A>T (p.Ser3424=)
c.5869+4137A>T (n.5869+4137A>T)
2g.21006596T>CCA425343495APOBc.10272A>G (p.Ser3424=)
c.5869+4137A>G (n.5869+4137A>G)
2g.21006596T>GCA425343497APOBc.10272A>C (p.Ser3424=)
c.5869+4137A>C (n.5869+4137A>C)
dbSNP
2g.21006596T=CA2493474868APOBc.10272A= (p.Ser3424=)
c.5869+4137A= (n.5869+4137A=)
2g.21006597G>ACA345986891APOBc.10271C>T (p.Ser3424Leu)
c.5869+4136C>T (n.5869+4136C>T)
2g.21006597G>CCA345986892APOBc.10271C>G (p.Ser3424Ter)
c.5869+4136C>G (n.5869+4136C>G)
2g.21006597G>TCA345986893APOBc.10271C>A (p.Ser3424Ter)
c.5869+4136C>A (n.5869+4136C>A)
gnomAD v4
2g.21006598A=CA2493474869APOBc.10270T= (p.Ser3424=)
c.5869+4135T= (n.5869+4135T=)
2g.21006598A>CCA345986894APOBc.10270T>G (p.Ser3424Ala)
c.5869+4135T>G (n.5869+4135T>G)
2g.21006598A>GCA345986896APOBc.10270T>C (p.Ser3424Pro)
c.5869+4135T>C (n.5869+4135T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006598A>TCA345986895APOBc.10270T>A (p.Ser3424Thr)
c.5869+4135T>A (n.5869+4135T>A)
dbSNP gnomAD v2 gnomAD v4
2g.21006599C>ACA425343501APOBc.10269G>T (p.Val3423=)
c.5869+4134G>T (n.5869+4134G>T)
gnomAD v4
2g.21006599C=CA2493474870APOBc.10269G= (p.Val3423=)
c.5869+4134G= (n.5869+4134G=)
2g.21006599C>GCA042953APOBc.10269G>C (p.Val3423=)
c.5869+4134G>C (n.5869+4134G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006599C>TCA425343502APOBc.10269G>A (p.Val3423=)
c.5869+4134G>A (n.5869+4134G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006600A=CA2493474871APOBc.10268T= (p.Val3423=)
c.5869+4133T= (n.5869+4133T=)
2g.21006600A>CCA345986897APOBc.10268T>G (p.Val3423Gly)
c.5869+4133T>G (n.5869+4133T>G)
2g.21006600A>GCA43496164APOBc.10268T>C (p.Val3423Ala)
c.5869+4133T>C (n.5869+4133T>C)
dbSNP gnomAD v4 COSMIC
2g.21006600A>TCA345986898APOBc.10268T>A (p.Val3423Glu)
c.5869+4133T>A (n.5869+4133T>A)
2g.21006601C>ACA345986899APOBc.10267G>T (p.Val3423Leu)
c.5869+4132G>T (n.5869+4132G>T)
2g.21006601C=CA2493474872APOBc.10267G= (p.Val3423=)
c.5869+4132G= (n.5869+4132G=)
2g.21006601C>GCA345986900APOBc.10267G>C (p.Val3423Leu)
c.5869+4132G>C (n.5869+4132G>C)
2g.21006601C>TCA042928APOBc.10267G>A (p.Val3423Met)
c.5869+4132G>A (n.5869+4132G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006602T>ACA345986901APOBc.10266A>T (p.Glu3422Asp)
c.5869+4131A>T (n.5869+4131A>T)
2g.21006602T>CCA425343504APOBc.10266A>G (p.Glu3422=)
c.5869+4131A>G (n.5869+4131A>G)
2g.21006602T>GCA43496178APOBc.10266A>C (p.Glu3422Asp)
c.5869+4131A>C (n.5869+4131A>C)
dbSNP
2g.21006602T=CA2493474873APOBc.10266A= (p.Glu3422=)
c.5869+4131A= (n.5869+4131A=)
2g.21006603T>ACA345986903APOBc.10265A>T (p.Glu3422Val)
c.5869+4130A>T (n.5869+4130A>T)
2g.21006603T>CCA042911APOBc.10265A>G (p.Glu3422Gly)
c.5869+4130A>G (n.5869+4130A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006603T>GCA345986902APOBc.10265A>C (p.Glu3422Ala)
c.5869+4130A>C (n.5869+4130A>C)
gnomAD v4
2g.21006603T=CA2493474874APOBc.10265A= (p.Glu3422=)
c.5869+4130A= (n.5869+4130A=)
2g.21006604C>ACA345986904APOBc.10264G>T (p.Glu3422Ter)
c.5869+4129G>T (n.5869+4129G>T)
2g.21006604C>GCA345986905APOBc.10264G>C (p.Glu3422Gln)
c.5869+4129G>C (n.5869+4129G>C)
2g.21006604C>TCA345986906APOBc.10264G>A (p.Glu3422Lys)
c.5869+4129G>A (n.5869+4129G>A)
COSMIC
2g.21006605C>ACA345986907APOBc.10263G>T (p.Met3421Ile)
c.5869+4128G>T (n.5869+4128G>T)
2g.21006605C>GCA345986908APOBc.10263G>C (p.Met3421Ile)
c.5869+4128G>C (n.5869+4128G>C)
2g.21006605C>TCA345986909APOBc.10263G>A (p.Met3421Ile)
c.5869+4128G>A (n.5869+4128G>A)
COSMIC
2g.21006606A=CA2493474875APOBc.10262T= (p.Met3421=)
c.5869+4127T= (n.5869+4127T=)
2g.21006606A>CCA345986910APOBc.10262T>G (p.Met3421Arg)
c.5869+4127T>G (n.5869+4127T>G)
2g.21006606A>GCA042900APOBc.10262T>C (p.Met3421Thr)
c.5869+4127T>C (n.5869+4127T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006606A>TCA345986911APOBc.10262T>A (p.Met3421Lys)
c.5869+4127T>A (n.5869+4127T>A)
2g.21006607T>ACA345986912APOBc.10261A>T (p.Met3421Leu)
c.5869+4126A>T (n.5869+4126A>T)
2g.21006607T>CCA345986913APOBc.10261A>G (p.Met3421Val)
c.5869+4126A>G (n.5869+4126A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21006607T>GCA345986914APOBc.10261A>C (p.Met3421Leu)
c.5869+4126A>C (n.5869+4126A>C)
2g.21006607T=CA2493474876APOBc.10261A= (p.Met3421=)
c.5869+4126A= (n.5869+4126A=)
2g.21006608A=CA2493474877APOBc.10260T= (p.Asn3420=)
c.5869+4125T= (n.5869+4125T=)
2g.21006608A>CCA345986916APOBc.10260T>G (p.Asn3420Lys)
c.5869+4125T>G (n.5869+4125T>G)
2g.21006608A>GCA425343514APOBc.10260T>C (p.Asn3420=)
c.5869+4125T>C (n.5869+4125T>C)
2g.21006608A>TCA345986915APOBc.10260T>A (p.Asn3420Lys)
c.5869+4125T>A (n.5869+4125T>A)
dbSNP
2g.21006609T>ACA345986917APOBc.10259A>T (p.Asn3420Ile)
c.5869+4124A>T (n.5869+4124A>T)
2g.21006609T>CCA345986918APOBc.10259A>G (p.Asn3420Ser)
c.5869+4124A>G (n.5869+4124A>G)
2g.21006609T>GCA345986919APOBc.10259A>C (p.Asn3420Thr)
c.5869+4124A>C (n.5869+4124A>C)
2g.21006613delCA2576686508APOBc.10259del (p.Asn3420IlefsTer17)
c.5869+4124del (n.5869+4124del)
2g.21006610T>ACA345986920APOBc.10258A>T (p.Asn3420Tyr)
c.5869+4123A>T (n.5869+4123A>T)
2g.21006610T>CCA345986921APOBc.10258A>G (p.Asn3420Asp)
c.5869+4123A>G (n.5869+4123A>G)
2g.21006610T>GCA345986922APOBc.10258A>C (p.Asn3420His)
c.5869+4123A>C (n.5869+4123A>C)
2g.21006611T>ACA345986923APOBc.10257A>T (p.Lys3419Asn)
c.5869+4122A>T (n.5869+4122A>T)
2g.21006611T>CCA425343518APOBc.10257A>G (p.Lys3419=)
c.5869+4122A>G (n.5869+4122A>G)
2g.21006611T>GCA345986924APOBc.10257A>C (p.Lys3419Asn)
c.5869+4122A>C (n.5869+4122A>C)
2g.21006612T>ACA345986925APOBc.10256A>T (p.Lys3419Ile)
c.5869+4121A>T (n.5869+4121A>T)
2g.21006612T>CCA345986926APOBc.10256A>G (p.Lys3419Arg)
c.5869+4121A>G (n.5869+4121A>G)
dbSNP
2g.21006612T>GCA345986927APOBc.10256A>C (p.Lys3419Thr)
c.5869+4121A>C (n.5869+4121A>C)
COSMIC
2g.21006612T=CA2493474878APOBc.10256A= (p.Lys3419=)
c.5869+4121A= (n.5869+4121A=)
2g.21006613T>ACA345986928APOBc.10255A>T (p.Lys3419Ter)
c.5869+4120A>T (n.5869+4120A>T)
2g.21006613T>CCA345986929APOBc.10255A>G (p.Lys3419Glu)
c.5869+4120A>G (n.5869+4120A>G)
gnomAD v4
2g.21006613T>GCA345986930APOBc.10255A>C (p.Lys3419Gln)
c.5869+4120A>C (n.5869+4120A>C)
2g.21006614C>ACA425343523APOBc.10254G>T (p.Thr3418=)
c.5869+4119G>T (n.5869+4119G>T)
2g.21006614C=CA2493474879APOBc.10254G= (p.Thr3418=)
c.5869+4119G= (n.5869+4119G=)
2g.21006614C>GCA425343524APOBc.10254G>C (p.Thr3418=)
c.5869+4119G>C (n.5869+4119G>C)
2g.21006614C>TCA042878APOBc.10254G>A (p.Thr3418=)
c.5869+4119G>A (n.5869+4119G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21006615G>ACA042865APOBc.10253C>T (p.Thr3418Met)
c.5869+4118C>T (n.5869+4118C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21006615G>CCA345986931APOBc.10253C>G (p.Thr3418Arg)
c.5869+4118C>G (n.5869+4118C>G)
2g.21006615G=CA2493474880APOBc.10253C= (p.Thr3418=)
c.5869+4118C= (n.5869+4118C=)
2g.21006615G>TCA43496251APOBc.10253C>A (p.Thr3418Lys)
c.5869+4118C>A (n.5869+4118C>A)
dbSNP
2g.21006616T>ACA345986932APOBc.10252A>T (p.Thr3418Ser)
c.5869+4117A>T (n.5869+4117A>T)
2g.21006616T>CCA345986933APOBc.10252A>G (p.Thr3418Ala)
c.5869+4117A>G (n.5869+4117A>G)
gnomAD v4
2g.21006616T>GCA345986934APOBc.10252A>C (p.Thr3418Pro)
c.5869+4117A>C (n.5869+4117A>C)
2g.21006617G>ACA042853APOBc.10251C>T (p.Thr3417=)
c.5869+4116C>T (n.5869+4116C>T)
dbSNP ExAC gnomAD v2
2g.21006617G>CCA425343528APOBc.10251C>G (p.Thr3417=)
c.5869+4116C>G (n.5869+4116C>G)
2g.21006617G=CA2493474881APOBc.10251C= (p.Thr3417=)
c.5869+4116C= (n.5869+4116C=)
2g.21006617G>TCA425343529APOBc.10251C>A (p.Thr3417=)
c.5869+4116C>A (n.5869+4116C>A)
COSMIC
2g.21006618G>ACA345986937APOBc.10250C>T (p.Thr3417Ile)
c.5869+4115C>T (n.5869+4115C>T)
2g.21006618G>CCA345986935APOBc.10250C>G (p.Thr3417Ser)
c.5869+4115C>G (n.5869+4115C>G)
2g.21006618G=CA2493474882APOBc.10250C= (p.Thr3417=)
c.5869+4115C= (n.5869+4115C=)
2g.21006618G>TCA345986936APOBc.10250C>A (p.Thr3417Asn)
c.5869+4115C>A (n.5869+4115C>A)
dbSNP gnomAD v4
2g.21006619T>ACA345986938APOBc.10249A>T (p.Thr3417Ser)
c.5869+4114A>T (n.5869+4114A>T)
2g.21006619T>CCA345986939APOBc.10249A>G (p.Thr3417Ala)
c.5869+4114A>G (n.5869+4114A>G)
gnomAD v4
2g.21006619T>GCA345986940APOBc.10249A>C (p.Thr3417Pro)
c.5869+4114A>C (n.5869+4114A>C)
2g.21006620T>ACA345986941APOBc.10248A>T (p.Leu3416Phe)
c.5869+4113A>T (n.5869+4113A>T)
2g.21006620T>CCA425343532APOBc.10248A>G (p.Leu3416=)
c.5869+4113A>G (n.5869+4113A>G)
2g.21006620T>GCA345986942APOBc.10248A>C (p.Leu3416Phe)
c.5869+4113A>C (n.5869+4113A>C)
gnomAD v4
2g.21006621A>CCA345986945APOBc.10247T>G (p.Leu3416Ter)
c.5869+4112T>G (n.5869+4112T>G)
2g.21006621A>GCA345986943APOBc.10247T>C (p.Leu3416Ser)
c.5869+4112T>C (n.5869+4112T>C)
2g.21006621A>TCA345986944APOBc.10247T>A (p.Leu3416Ter)
c.5869+4112T>A (n.5869+4112T>A)
2g.21006622A=CA2493474883APOBc.10246T= (p.Leu3416=)
c.5869+4111T= (n.5869+4111T=)
2g.21006622A>CCA345986946APOBc.10246T>G (p.Leu3416Val)
c.5869+4111T>G (n.5869+4111T>G)
2g.21006622A>GCA425343536APOBc.10246T>C (p.Leu3416=)
c.5869+4111T>C (n.5869+4111T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21006622A>TCA345986947APOBc.10246T>A (p.Leu3416Ile)
c.5869+4111T>A (n.5869+4111T>A)
gnomAD v4
2g.21006623G>ACA425343537APOBc.10245C>T (p.Ser3415=)
c.5869+4110C>T (n.5869+4110C>T)
dbSNP gnomAD v2 gnomAD v4
2g.21006623G>CCA345986948APOBc.10245C>G (p.Ser3415Arg)
c.5869+4110C>G (n.5869+4110C>G)
2g.21006623G=CA2493474884APOBc.10245C= (p.Ser3415=)
c.5869+4110C= (n.5869+4110C=)
2g.21006623G>TCA345986949APOBc.10245C>A (p.Ser3415Arg)
c.5869+4110C>A (n.5869+4110C>A)
COSMIC
2g.21006624C>ACA345986950APOBc.10244G>T (p.Ser3415Ile)
c.5869+4109G>T (n.5869+4109G>T)
2g.21006624C=CA2493474885APOBc.10244G= (p.Ser3415=)
c.5869+4109G= (n.5869+4109G=)
2g.21006624C>GCA042839APOBc.10244G>C (p.Ser3415Thr)
c.5869+4109G>C (n.5869+4109G>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21006624C>TCA345986951APOBc.10244G>A (p.Ser3415Asn)
c.5869+4109G>A (n.5869+4109G>A)
gnomAD v4
2g.21006625T>ACA345986952APOBc.10243A>T (p.Ser3415Cys)
c.5869+4108A>T (n.5869+4108A>T)
2g.21006625T>CCA345986953APOBc.10243A>G (p.Ser3415Gly)
c.5869+4108A>G (n.5869+4108A>G)
2g.21006625T>GCA345986954APOBc.10243A>C (p.Ser3415Arg)
c.5869+4108A>C (n.5869+4108A>C)
2g.21006626C>ACA425343538APOBc.10242G>T (p.Val3414=)
c.5869+4107G>T (n.5869+4107G>T)
2g.21006626C>GCA425343541APOBc.10242G>C (p.Val3414=)
c.5869+4107G>C (n.5869+4107G>C)
2g.21006626C>TCA425343544APOBc.10242G>A (p.Val3414=)
c.5869+4107G>A (n.5869+4107G>A)
ClinVar

Number of alleles fetched