Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21005084delCA2658074510APOBc.11786del (p.Asn3929MetfsTer13)
c.5869+5651del (n.5869+5651del)
 gnomAD v4
2g.21005084T>ACA425136011APOBc.11784A>T (p.Leu3928=)
c.5869+5649A>T (n.5869+5649A>T)
2g.21005084T>CCA425136012APOBc.11784A>G (p.Leu3928=)
c.5869+5649A>G (n.5869+5649A>G)
2g.21005084T>GCA425136013APOBc.11784A>C (p.Leu3928=)
c.5869+5649A>C (n.5869+5649A>C)
2g.21005085A=CA2493474243APOBc.11783T= (p.Leu3928=)
c.5869+5648T= (n.5869+5648T=)
2g.21005085A>CCA345977172APOBc.11783T>G (p.Leu3928Arg)
c.5869+5648T>G (n.5869+5648T>G)
2g.21005085A>GCA345977184APOBc.11783T>C (p.Leu3928Pro)
c.5869+5648T>C (n.5869+5648T>C)
2g.21005085A>TCA047397APOBc.11783T>A (p.Leu3928Gln)
c.5869+5648T>A (n.5869+5648T>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005086G>ACA425136014APOBc.11782C>T (p.Leu3928=)
c.5869+5647C>T (n.5869+5647C>T)
 ClinVar dbSNP gnomAD v4
2g.21005086G>CCA345977190APOBc.11782C>G (p.Leu3928Val)
c.5869+5647C>G (n.5869+5647C>G)
2g.21005086G=CA2493474244APOBc.11782C= (p.Leu3928=)
c.5869+5647C= (n.5869+5647C=)
2g.21005086G>TCA047385APOBc.11782C>A (p.Leu3928Ile)
c.5869+5647C>A (n.5869+5647C>A)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005087T>ACA345977200APOBc.11781A>T (p.Glu3927Asp)
c.5869+5646A>T (n.5869+5646A>T)
2g.21005087T>CCA425136015APOBc.11781A>G (p.Glu3927=)
c.5869+5646A>G (n.5869+5646A>G)
2g.21005087T>GCA345977203APOBc.11781A>C (p.Glu3927Asp)
c.5869+5646A>C (n.5869+5646A>C)
2g.21005088T>ACA345977209APOBc.11780A>T (p.Glu3927Val)
c.5869+5645A>T (n.5869+5645A>T)
2g.21005088T>CCA345977205APOBc.11780A>G (p.Glu3927Gly)
c.5869+5645A>G (n.5869+5645A>G)
2g.21005088T>GCA345977207APOBc.11780A>C (p.Glu3927Ala)
c.5869+5645A>C (n.5869+5645A>C)
2g.21005089C>ACA345977216APOBc.11779G>T (p.Glu3927Ter)
c.5869+5644G>T (n.5869+5644G>T)
2g.21005089C>GCA345977222APOBc.11779G>C (p.Glu3927Gln)
c.5869+5644G>C (n.5869+5644G>C)
2g.21005089C>TCA345977225APOBc.11779G>A (p.Glu3927Lys)
c.5869+5644G>A (n.5869+5644G>A)
 COSMIC
2g.21005090A>CCA345977231APOBc.11778T>G (p.Tyr3926Ter)
c.5869+5643T>G (n.5869+5643T>G)
2g.21005090A>GCA425136016APOBc.11778T>C (p.Tyr3926=)
c.5869+5643T>C (n.5869+5643T>C)
2g.21005090A>TCA345977237APOBc.11778T>A (p.Tyr3926Ter)
c.5869+5643T>A (n.5869+5643T>A)
2g.21005091T>ACA345977240APOBc.11777A>T (p.Tyr3926Phe)
c.5869+5642A>T (n.5869+5642A>T)
2g.21005091T>CCA047364APOBc.11777A>G (p.Tyr3926Cys)
c.5869+5642A>G (n.5869+5642A>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005091T>GCA345977245APOBc.11777A>C (p.Tyr3926Ser)
c.5869+5642A>C (n.5869+5642A>C)
2g.21005091T=CA2493474245APOBc.11777A= (p.Tyr3926=)
c.5869+5642A= (n.5869+5642A=)
2g.21005092A=CA2493474246APOBc.11776T= (p.Tyr3926=)
c.5869+5641T= (n.5869+5641T=)
2g.21005092A>CCA345977260APOBc.11776T>G (p.Tyr3926Asp)
c.5869+5641T>G (n.5869+5641T>G)
2g.21005092A>GCA345977262APOBc.11776T>C (p.Tyr3926His)
c.5869+5641T>C (n.5869+5641T>C)
 dbSNP gnomAD v4
2g.21005092A>TCA345977263APOBc.11776T>A (p.Tyr3926Asn)
c.5869+5641T>A (n.5869+5641T>A)
2g.21005093T>ACA345977280APOBc.11775A>T (p.Glu3925Asp)
c.5869+5640A>T (n.5869+5640A>T)
2g.21005093T>CCA425136017APOBc.11775A>G (p.Glu3925=)
c.5869+5640A>G (n.5869+5640A>G)
 dbSNP gnomAD v4
2g.21005093T>GCA345977272APOBc.11775A>C (p.Glu3925Asp)
c.5869+5640A>C (n.5869+5640A>C)
2g.21005093T=CA2493474247APOBc.11775A= (p.Glu3925=)
c.5869+5640A= (n.5869+5640A=)
2g.21005094T>ACA345977296APOBc.11774A>T (p.Glu3925Val)
c.5869+5639A>T (n.5869+5639A>T)
2g.21005094T>CCA345977298APOBc.11774A>G (p.Glu3925Gly)
c.5869+5639A>G (n.5869+5639A>G)
2g.21005094T>GCA345977300APOBc.11774A>C (p.Glu3925Ala)
c.5869+5639A>C (n.5869+5639A>C)
2g.21005095C>ACA345977304APOBc.11773G>T (p.Glu3925Ter)
c.5869+5638G>T (n.5869+5638G>T)
2g.21005095C>GCA345977306APOBc.11773G>C (p.Glu3925Gln)
c.5869+5638G>C (n.5869+5638G>C)
2g.21005095C>TCA345977309APOBc.11773G>A (p.Glu3925Lys)
c.5869+5638G>A (n.5869+5638G>A)
2g.21005096T>ACA425136020APOBc.11772A>T (p.Leu3924=)
c.5869+5637A>T (n.5869+5637A>T)
2g.21005096T>CCA425136019APOBc.11772A>G (p.Leu3924=)
c.5869+5637A>G (n.5869+5637A>G)
 dbSNP gnomAD v4
2g.21005096T>GCA425136021APOBc.11772A>C (p.Leu3924=)
c.5869+5637A>C (n.5869+5637A>C)
2g.21005096T=CA2493474248APOBc.11772A= (p.Leu3924=)
c.5869+5637A= (n.5869+5637A=)
2g.21005097A>CCA345977314APOBc.11771T>G (p.Leu3924Arg)
c.5869+5636T>G (n.5869+5636T>G)
2g.21005097A>GCA345977311APOBc.11771T>C (p.Leu3924Pro)
c.5869+5636T>C (n.5869+5636T>C)
 gnomAD v4
2g.21005097A>TCA345977313APOBc.11771T>A (p.Leu3924Gln)
c.5869+5636T>A (n.5869+5636T>A)
2g.21005098G>ACA425136022APOBc.11770C>T (p.Leu3924=)
c.5869+5635C>T (n.5869+5635C>T)
2g.21005098G>CCA345977316APOBc.11770C>G (p.Leu3924Val)
c.5869+5635C>G (n.5869+5635C>G)
 ClinVar gnomAD v4
2g.21005098G>TCA345977319APOBc.11770C>A (p.Leu3924Ile)
c.5869+5635C>A (n.5869+5635C>A)
2g.21005099G>ACA047352APOBc.11769C>T (p.Phe3923=)
c.5869+5634C>T (n.5869+5634C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.21005099G>CCA345977331APOBc.11769C>G (p.Phe3923Leu)
c.5869+5634C>G (n.5869+5634C>G)
2g.21005099G=CA2493474249APOBc.11769C= (p.Phe3923=)
c.5869+5634C= (n.5869+5634C=)
2g.21005099G>TCA345977334APOBc.11769C>A (p.Phe3923Leu)
c.5869+5634C>A (n.5869+5634C>A)
 dbSNP
2g.21005100A>CCA345977338APOBc.11768T>G (p.Phe3923Cys)
c.5869+5633T>G (n.5869+5633T>G)
 gnomAD v4
2g.21005100A>GCA345977342APOBc.11768T>C (p.Phe3923Ser)
c.5869+5633T>C (n.5869+5633T>C)
2g.21005100A>TCA345977339APOBc.11768T>A (p.Phe3923Tyr)
c.5869+5633T>A (n.5869+5633T>A)
2g.21005101A=CA2493474250APOBc.11767T= (p.Phe3923=)
c.5869+5632T= (n.5869+5632T=)
2g.21005101A>CCA345977346APOBc.11767T>G (p.Phe3923Val)
c.5869+5632T>G (n.5869+5632T>G)
2g.21005101A>GCA345977349APOBc.11767T>C (p.Phe3923Leu)
c.5869+5632T>C (n.5869+5632T>C)
2g.21005101A>TCA345977352APOBc.11767T>A (p.Phe3923Ile)
c.5869+5632T>A (n.5869+5632T>A)
 dbSNP
2g.21005102C>ACA345977354APOBc.11766G>T (p.Gln3922His)
c.5869+5631G>T (n.5869+5631G>T)
2g.21005102C>GCA345977356APOBc.11766G>C (p.Gln3922His)
c.5869+5631G>C (n.5869+5631G>C)
2g.21005102C>TCA425136023APOBc.11766G>A (p.Gln3922=)
c.5869+5631G>A (n.5869+5631G>A)
2g.21005103T>ACA345977361APOBc.11765A>T (p.Gln3922Leu)
c.5869+5630A>T (n.5869+5630A>T)
2g.21005103T>CCA345977364APOBc.11765A>G (p.Gln3922Arg)
c.5869+5630A>G (n.5869+5630A>G)
2g.21005103T>GCA345977365APOBc.11765A>C (p.Gln3922Pro)
c.5869+5630A>C (n.5869+5630A>C)
2g.21005104G>ACA345977374APOBc.11764C>T (p.Gln3922Ter)
c.5869+5629C>T (n.5869+5629C>T)
 ClinVar dbSNP
2g.21005104G>CCA047342APOBc.11764C>G (p.Gln3922Glu)
c.5869+5629C>G (n.5869+5629C>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005104G=CA2493474251APOBc.11764C= (p.Gln3922=)
c.5869+5629C= (n.5869+5629C=)
2g.21005104G>TCA345977377APOBc.11764C>A (p.Gln3922Lys)
c.5869+5629C>A (n.5869+5629C>A)
2g.21005105T>ACA425136024APOBc.11763A>T (p.Val3921=)
c.5869+5628A>T (n.5869+5628A>T)
2g.21005105T>CCA425136025APOBc.11763A>G (p.Val3921=)
c.5869+5628A>G (n.5869+5628A>G)
 ClinVar dbSNP gnomAD v4
2g.21005105T>GCA425136026APOBc.11763A>C (p.Val3921=)
c.5869+5628A>C (n.5869+5628A>C)
2g.21005105T=CA2493474252APOBc.11763A= (p.Val3921=)
c.5869+5628A= (n.5869+5628A=)
2g.21005106A>CCA345977381APOBc.11762T>G (p.Val3921Gly)
c.5869+5627T>G (n.5869+5627T>G)
2g.21005106A>GCA345977384APOBc.11762T>C (p.Val3921Ala)
c.5869+5627T>C (n.5869+5627T>C)
2g.21005106A>TCA345977380APOBc.11762T>A (p.Val3921Glu)
c.5869+5627T>A (n.5869+5627T>A)
2g.21005107C>ACA345977385APOBc.11761G>T (p.Val3921Leu)
c.5869+5626G>T (n.5869+5626G>T)
 dbSNP gnomAD v4
2g.21005107C=CA2493474253APOBc.11761G= (p.Val3921=)
c.5869+5626G= (n.5869+5626G=)
2g.21005107C>GCA345977386APOBc.11761G>C (p.Val3921Leu)
c.5869+5626G>C (n.5869+5626G>C)
2g.21005107C>TCA047332APOBc.11761G>A (p.Val3921Ile)
c.5869+5626G>A (n.5869+5626G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21005107_21005110delCA645535044APOBc.11758_11761del (p.Thr3920TyrfsTer4)
c.5869+5623_5869+5626del (n.5869+5623_5869+5626del)
 COSMIC
2g.21005108G>ACA047317APOBc.11760C>T (p.Thr3920=)
c.5869+5625C>T (n.5869+5625C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005108G>CCA425136027APOBc.11760C>G (p.Thr3920=)
c.5869+5625C>G (n.5869+5625C>G)
2g.21005108G=CA2493474254APOBc.11760C= (p.Thr3920=)
c.5869+5625C= (n.5869+5625C=)
2g.21005108G>TCA425136028APOBc.11760C>A (p.Thr3920=)
c.5869+5625C>A (n.5869+5625C>A)
2g.21005109G>ACA345977394APOBc.11759C>T (p.Thr3920Ile)
c.5869+5624C>T (n.5869+5624C>T)
 dbSNP gnomAD v2 gnomAD v4
2g.21005109G>CCA345977396APOBc.11759C>G (p.Thr3920Ser)
c.5869+5624C>G (n.5869+5624C>G)
2g.21005109G=CA2493474255APOBc.11759C= (p.Thr3920=)
c.5869+5624C= (n.5869+5624C=)
2g.21005109G>TCA345977397APOBc.11759C>A (p.Thr3920Asn)
c.5869+5624C>A (n.5869+5624C>A)
2g.21005110T>ACA345977399APOBc.11758A>T (p.Thr3920Ser)
c.5869+5623A>T (n.5869+5623A>T)
2g.21005110T>CCA345977400APOBc.11758A>G (p.Thr3920Ala)
c.5869+5623A>G (n.5869+5623A>G)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.21005110T>GCA345977401APOBc.11758A>C (p.Thr3920Pro)
c.5869+5623A>C (n.5869+5623A>C)
2g.21005110T=CA2493474256APOBc.11758A= (p.Thr3920=)
c.5869+5623A= (n.5869+5623A=)
2g.21005111T>ACA425136031APOBc.11757A>T (p.Ser3919=)
c.5869+5622A>T (n.5869+5622A>T)
2g.21005111T>CCA425136029APOBc.11757A>G (p.Ser3919=)
c.5869+5622A>G (n.5869+5622A>G)
2g.21005111T>GCA425136030APOBc.11757A>C (p.Ser3919=)
c.5869+5622A>C (n.5869+5622A>C)
2g.21005112G>ACA345977402APOBc.11756C>T (p.Ser3919Leu)
c.5869+5621C>T (n.5869+5621C>T)
 dbSNP gnomAD v3 gnomAD v4
2g.21005112G>CCA345977403APOBc.11756C>G (p.Ser3919Ter)
c.5869+5621C>G (n.5869+5621C>G)
2g.21005112G=CA2493474257APOBc.11756C= (p.Ser3919=)
c.5869+5621C= (n.5869+5621C=)
2g.21005112G>TCA345977404APOBc.11756C>A (p.Ser3919Ter)
c.5869+5621C>A (n.5869+5621C>A)
2g.21005113A>CCA345977413APOBc.11755T>G (p.Ser3919Ala)
c.5869+5620T>G (n.5869+5620T>G)
2g.21005113A>GCA345977407APOBc.11755T>C (p.Ser3919Pro)
c.5869+5620T>C (n.5869+5620T>C)
2g.21005113A>TCA345977406APOBc.11755T>A (p.Ser3919Thr)
c.5869+5620T>A (n.5869+5620T>A)
2g.21005114G>ACA425136032APOBc.11754C>T (p.Ser3918=)
c.5869+5619C>T (n.5869+5619C>T)
2g.21005114G>CCA345977415APOBc.11754C>G (p.Ser3918Arg)
c.5869+5619C>G (n.5869+5619C>G)
2g.21005114G>TCA345977420APOBc.11754C>A (p.Ser3918Arg)
c.5869+5619C>A (n.5869+5619C>A)
2g.21005115C>ACA345977423APOBc.11753G>T (p.Ser3918Ile)
c.5869+5618G>T (n.5869+5618G>T)
2g.21005115C>GCA345977428APOBc.11753G>C (p.Ser3918Thr)
c.5869+5618G>C (n.5869+5618G>C)
2g.21005115C>TCA345977429APOBc.11753G>A (p.Ser3918Asn)
c.5869+5618G>A (n.5869+5618G>A)
2g.21005116T>ACA345977431APOBc.11752A>T (p.Ser3918Cys)
c.5869+5617A>T (n.5869+5617A>T)
2g.21005116T>CCA345977433APOBc.11752A>G (p.Ser3918Gly)
c.5869+5617A>G (n.5869+5617A>G)
2g.21005116T>GCA345977434APOBc.11752A>C (p.Ser3918Arg)
c.5869+5617A>C (n.5869+5617A>C)
2g.21005117G>ACA047307APOBc.11751C>T (p.Cys3917=)
c.5869+5616C>T (n.5869+5616C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005117G>CCA345977435APOBc.11751C>G (p.Cys3917Trp)
c.5869+5616C>G (n.5869+5616C>G)
2g.21005117G=CA2493474258APOBc.11751C= (p.Cys3917=)
c.5869+5616C= (n.5869+5616C=)
2g.21005117G>TCA345977436APOBc.11751C>A (p.Cys3917Ter)
c.5869+5616C>A (n.5869+5616C>A)
2g.21005118C>ACA345977438APOBc.11750G>T (p.Cys3917Phe)
c.5869+5615G>T (n.5869+5615G>T)
 gnomAD v4
2g.21005118C>GCA345977440APOBc.11750G>C (p.Cys3917Ser)
c.5869+5615G>C (n.5869+5615G>C)
2g.21005118C>TCA345977441APOBc.11750G>A (p.Cys3917Tyr)
c.5869+5615G>A (n.5869+5615G>A)
 gnomAD v4
2g.21005119A=CA2493474259APOBc.11749T= (p.Cys3917=)
c.5869+5614T= (n.5869+5614T=)
2g.21005119A>CCA345977445APOBc.11749T>G (p.Cys3917Gly)
c.5869+5614T>G (n.5869+5614T>G)
2g.21005119A>GCA345977447APOBc.11749T>C (p.Cys3917Arg)
c.5869+5614T>C (n.5869+5614T>C)
 dbSNP gnomAD v2 gnomAD v4
2g.21005119A>TCA345977443APOBc.11749T>A (p.Cys3917Ser)
c.5869+5614T>A (n.5869+5614T>A)
 ClinVar gnomAD v4
2g.21005120delCA2658074570APOBc.11748del (p.Cys3917AlafsTer8)
c.5869+5613del (n.5869+5613del)
 gnomAD v4
2g.21005120T>ACA425136034APOBc.11748A>T (p.Thr3916=)
c.5869+5613A>T (n.5869+5613A>T)
2g.21005120T>CCA425136035APOBc.11748A>G (p.Thr3916=)
c.5869+5613A>G (n.5869+5613A>G)
2g.21005120T>GCA425136036APOBc.11748A>C (p.Thr3916=)
c.5869+5613A>C (n.5869+5613A>C)
2g.21005121G>ACA345977448APOBc.11747C>T (p.Thr3916Ile)
c.5869+5612C>T (n.5869+5612C>T)
2g.21005121G>CCA345977450APOBc.11747C>G (p.Thr3916Arg)
c.5869+5612C>G (n.5869+5612C>G)
2g.21005121G>TCA345977452APOBc.11747C>A (p.Thr3916Lys)
c.5869+5612C>A (n.5869+5612C>A)
2g.21005122T>ACA345977453APOBc.11746A>T (p.Thr3916Ser)
c.5869+5611A>T (n.5869+5611A>T)
2g.21005122T>CCA345977455APOBc.11746A>G (p.Thr3916Ala)
c.5869+5611A>G (n.5869+5611A>G)
 gnomAD v4
2g.21005122T>GCA345977456APOBc.11746A>C (p.Thr3916Pro)
c.5869+5611A>C (n.5869+5611A>C)
 dbSNP
2g.21005122T=CA2493474260APOBc.11746A= (p.Thr3916=)
c.5869+5611A= (n.5869+5611A=)
2g.21005123G>ACA425136037APOBc.11745C>T (p.Ser3915=)
c.5869+5610C>T (n.5869+5610C>T)
 dbSNP
2g.21005123G>CCA425136038APOBc.11745C>G (p.Ser3915=)
c.5869+5610C>G (n.5869+5610C>G)
2g.21005123G=CA2493474261APOBc.11745C= (p.Ser3915=)
c.5869+5610C= (n.5869+5610C=)
2g.21005123G>TCA425136039APOBc.11745C>A (p.Ser3915=)
c.5869+5610C>A (n.5869+5610C>A)
2g.21005124G>ACA047281APOBc.11744C>T (p.Ser3915Phe)
c.5869+5609C>T (n.5869+5609C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21005124G>CCA047261APOBc.11744C>G (p.Ser3915Cys)
c.5869+5609C>G (n.5869+5609C>G)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005124G=CA2493474262APOBc.11744C= (p.Ser3915=)
c.5869+5609C= (n.5869+5609C=)
2g.21005124G>TCA345977460APOBc.11744C>A (p.Ser3915Tyr)
c.5869+5609C>A (n.5869+5609C>A)
 gnomAD v4
2g.21005125A>CCA345977464APOBc.11743T>G (p.Ser3915Ala)
c.5869+5608T>G (n.5869+5608T>G)
2g.21005125A>GCA345977465APOBc.11743T>C (p.Ser3915Pro)
c.5869+5608T>C (n.5869+5608T>C)
2g.21005125A>TCA345977467APOBc.11743T>A (p.Ser3915Thr)
c.5869+5608T>A (n.5869+5608T>A)
2g.21005126A>CCA345977470APOBc.11742T>G (p.Asp3914Glu)
c.5869+5607T>G (n.5869+5607T>G)
2g.21005126A>GCA425136040APOBc.11742T>C (p.Asp3914=)
c.5869+5607T>C (n.5869+5607T>C)
2g.21005126A>TCA345977472APOBc.11742T>A (p.Asp3914Glu)
c.5869+5607T>A (n.5869+5607T>A)
2g.21005126_21005127insATTTCTTACCATTTAGTTCATATCA2749099409APOBc.11741_11742insATATGAACTAAATGGTAAGAAAT (p.Asp3914GlufsTer19)
c.5869+5606_5869+5607insATATGAACTAAATGGTAAGAAAT (n.5869+5606_5869+5607insATATGAACTAAATGGTAAGAAAT)
2g.21005127T>ACA345977474APOBc.11741A>T (p.Asp3914Val)
c.5869+5606A>T (n.5869+5606A>T)
2g.21005127T>CCA345977476APOBc.11741A>G (p.Asp3914Gly)
c.5869+5606A>G (n.5869+5606A>G)
2g.21005127T>GCA345977475APOBc.11741A>C (p.Asp3914Ala)
c.5869+5606A>C (n.5869+5606A>C)
2g.21005128C>ACA345977477APOBc.11740G>T (p.Asp3914Tyr)
c.5869+5605G>T (n.5869+5605G>T)
 dbSNP
2g.21005128C=CA2493474263APOBc.11740G= (p.Asp3914=)
c.5869+5605G= (n.5869+5605G=)
2g.21005128C>GCA047246APOBc.11740G>C (p.Asp3914His)
c.5869+5605G>C (n.5869+5605G>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005128C>TCA345977481APOBc.11740G>A (p.Asp3914Asn)
c.5869+5605G>A (n.5869+5605G>A)
2g.21005129C>ACA425136041APOBc.11739G>T (p.Leu3913=)
c.5869+5604G>T (n.5869+5604G>T)
2g.21005129C>GCA425136042APOBc.11739G>C (p.Leu3913=)
c.5869+5604G>C (n.5869+5604G>C)
 COSMIC
2g.21005129C>TCA425136043APOBc.11739G>A (p.Leu3913=)
c.5869+5604G>A (n.5869+5604G>A)
 dbSNP gnomAD v3 gnomAD v4
2g.21005130A>CCA345977483APOBc.11738T>G (p.Leu3913Arg)
c.5869+5603T>G (n.5869+5603T>G)
 gnomAD v4
2g.21005130A>GCA345977485APOBc.11738T>C (p.Leu3913Pro)
c.5869+5603T>C (n.5869+5603T>C)
2g.21005130A>TCA345977487APOBc.11738T>A (p.Leu3913Gln)
c.5869+5603T>A (n.5869+5603T>A)
2g.21005130_21005131delinsAGCA2493474264APOBc.11737_11738delinsCT (p.Leu3913=)
c.5869+5602_5869+5603delinsCT (n.5869+5602_5869+5603delinsCT)
2g.21005131G>ACA425136044APOBc.11737C>T (p.Leu3913=)
c.5869+5602C>T (n.5869+5602C>T)
2g.21005131G>CCA345977489APOBc.11737C>G (p.Leu3913Val)
c.5869+5602C>G (n.5869+5602C>G)
2g.21005131G>TCA345977491APOBc.11737C>A (p.Leu3913Met)
c.5869+5602C>A (n.5869+5602C>A)
2g.21005132delCA047232APOBc.11737del (p.Leu3913TrpfsTer12)
c.5869+5602del (n.5869+5602del)
 dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005132G>ACA425136047APOBc.11736C>T (p.Val3912=)
c.5869+5601C>T (n.5869+5601C>T)
2g.21005132G>CCA425136045APOBc.11736C>G (p.Val3912=)
c.5869+5601C>G (n.5869+5601C>G)
2g.21005132G>TCA425136046APOBc.11736C>A (p.Val3912=)
c.5869+5601C>A (n.5869+5601C>A)
 ClinVar gnomAD v4
2g.21005133A>CCA345977494APOBc.11735T>G (p.Val3912Gly)
c.5869+5600T>G (n.5869+5600T>G)
2g.21005133A>GCA345977496APOBc.11735T>C (p.Val3912Ala)
c.5869+5600T>C (n.5869+5600T>C)
2g.21005133A>TCA345977498APOBc.11735T>A (p.Val3912Asp)
c.5869+5600T>A (n.5869+5600T>A)
 gnomAD v4
2g.21005133_21005134insTTCA2576686487APOBc.11734_11735insAA (p.Val3912GlufsTer14)
c.5869+5599_5869+5600insAA (n.5869+5599_5869+5600insAA)
2g.21005134C>ACA345977500APOBc.11734G>T (p.Val3912Phe)
c.5869+5599G>T (n.5869+5599G>T)
2g.21005134C=CA2493474265APOBc.11734G= (p.Val3912=)
c.5869+5599G= (n.5869+5599G=)
2g.21005134C>GCA345977501APOBc.11734G>C (p.Val3912Leu)
c.5869+5599G>C (n.5869+5599G>C)
 gnomAD v4
2g.21005134C>TCA047218APOBc.11734G>A (p.Val3912Ile)
c.5869+5599G>A (n.5869+5599G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21005135T>ACA425136048APOBc.11733A>T (p.Thr3911=)
c.5869+5598A>T (n.5869+5598A>T)
 ClinVar dbSNP gnomAD v4
2g.21005135T>CCA425136049APOBc.11733A>G (p.Thr3911=)
c.5869+5598A>G (n.5869+5598A>G)
 gnomAD v4
2g.21005135T>GCA425136050APOBc.11733A>C (p.Thr3911=)
c.5869+5598A>C (n.5869+5598A>C)
2g.21005135T=CA2493474266APOBc.11733A= (p.Thr3911=)
c.5869+5598A= (n.5869+5598A=)
2g.21005136G>ACA345977504APOBc.11732C>T (p.Thr3911Ile)
c.5869+5597C>T (n.5869+5597C>T)
 gnomAD v4
2g.21005136G>CCA345977502APOBc.11732C>G (p.Thr3911Arg)
c.5869+5597C>G (n.5869+5597C>G)
 dbSNP
2g.21005136G=CA2493474267APOBc.11732C= (p.Thr3911=)
c.5869+5597C= (n.5869+5597C=)
2g.21005136G>TCA345977506APOBc.11732C>A (p.Thr3911Lys)
c.5869+5597C>A (n.5869+5597C>A)
2g.21005137T>ACA345977508APOBc.11731A>T (p.Thr3911Ser)
c.5869+5596A>T (n.5869+5596A>T)
2g.21005137T>CCA345977512APOBc.11731A>G (p.Thr3911Ala)
c.5869+5596A>G (n.5869+5596A>G)
2g.21005137T>GCA345977510APOBc.11731A>C (p.Thr3911Pro)
c.5869+5596A>C (n.5869+5596A>C)
2g.21005138T>ACA345977515APOBc.11730A>T (p.Glu3910Asp)
c.5869+5595A>T (n.5869+5595A>T)
 gnomAD v4
2g.21005138T>CCA425136051APOBc.11730A>G (p.Glu3910=)
c.5869+5595A>G (n.5869+5595A>G)
2g.21005138T>GCA345977516APOBc.11730A>C (p.Glu3910Asp)
c.5869+5595A>C (n.5869+5595A>C)
2g.21005139T>ACA345977519APOBc.11729A>T (p.Glu3910Val)
c.5869+5594A>T (n.5869+5594A>T)
2g.21005139T>CCA345977521APOBc.11729A>G (p.Glu3910Gly)
c.5869+5594A>G (n.5869+5594A>G)
2g.21005139T>GCA345977522APOBc.11729A>C (p.Glu3910Ala)
c.5869+5594A>C (n.5869+5594A>C)
2g.21005139_21005142delinsTCAACA2493474268APOBc.11726_11729delinsTTGA (p.Val3909=)
c.5869+5591_5869+5594delinsTTGA (n.5869+5591_5869+5594delinsTTGA)
2g.21005140C>ACA345977524APOBc.11728G>T (p.Glu3910Ter)
c.5869+5593G>T (n.5869+5593G>T)
 gnomAD v4 COSMIC
2g.21005140C>GCA345977526APOBc.11728G>C (p.Glu3910Gln)
c.5869+5593G>C (n.5869+5593G>C)
 gnomAD v4
2g.21005140C>TCA345977528APOBc.11728G>A (p.Glu3910Lys)
c.5869+5593G>A (n.5869+5593G>A)
 gnomAD v4 COSMIC
2g.21005142_21005144delCA530863358APOBc.11726_11728del (p.Val3909del)
c.5869+5591_5869+5593del (n.5869+5591_5869+5593del)
 dbSNP gnomAD v2 gnomAD v4
2g.21005141A>CCA425136052APOBc.11727T>G (p.Val3909=)
c.5869+5592T>G (n.5869+5592T>G)
2g.21005141A>GCA425136053APOBc.11727T>C (p.Val3909=)
c.5869+5592T>C (n.5869+5592T>C)
2g.21005141A>TCA425136054APOBc.11727T>A (p.Val3909=)
c.5869+5592T>A (n.5869+5592T>A)
2g.21005142A>CCA345977530APOBc.11726T>G (p.Val3909Gly)
c.5869+5591T>G (n.5869+5591T>G)
2g.21005142A>GCA345977532APOBc.11726T>C (p.Val3909Ala)
c.5869+5591T>C (n.5869+5591T>C)
2g.21005142A>TCA345977534APOBc.11726T>A (p.Val3909Asp)
c.5869+5591T>A (n.5869+5591T>A)
2g.21005143C>ACA345977540APOBc.11725G>T (p.Val3909Phe)
c.5869+5590G>T (n.5869+5590G>T)
2g.21005143C=CA2493474269APOBc.11725G= (p.Val3909=)
c.5869+5590G= (n.5869+5590G=)
2g.21005143C>GCA345977537APOBc.11725G>C (p.Val3909Leu)
c.5869+5590G>C (n.5869+5590G>C)
2g.21005143C>TCA345977538APOBc.11725G>A (p.Val3909Ile)
c.5869+5590G>A (n.5869+5590G>A)
 dbSNP
2g.21005144A>CCA345977543APOBc.11724T>G (p.Tyr3908Ter)
c.5869+5589T>G (n.5869+5589T>G)
2g.21005144A>GCA425136055APOBc.11724T>C (p.Tyr3908=)
c.5869+5589T>C (n.5869+5589T>C)
2g.21005144A>TCA345977544APOBc.11724T>A (p.Tyr3908Ter)
c.5869+5589T>A (n.5869+5589T>A)
2g.21005145_21005146delCA2698845806APOBc.11723_11724del (p.Tyr3908CysfsTer2)
c.5869+5588_5869+5589del (n.5869+5588_5869+5589del)
 dbSNP
2g.21005145T>ACA345977546APOBc.11723A>T (p.Tyr3908Phe)
c.5869+5588A>T (n.5869+5588A>T)
2g.21005145T>CCA345977548APOBc.11723A>G (p.Tyr3908Cys)
c.5869+5588A>G (n.5869+5588A>G)
2g.21005145T>GCA345977550APOBc.11723A>C (p.Tyr3908Ser)
c.5869+5588A>C (n.5869+5588A>C)
2g.21005146A=CA2493474270APOBc.11722T= (p.Tyr3908=)
c.5869+5587T= (n.5869+5587T=)
2g.21005146A>CCA345977552APOBc.11722T>G (p.Tyr3908Asp)
c.5869+5587T>G (n.5869+5587T>G)
 gnomAD v4
2g.21005146A>GCA43491494APOBc.11722T>C (p.Tyr3908His)
c.5869+5587T>C (n.5869+5587T>C)
 dbSNP
2g.21005146A>TCA345977555APOBc.11722T>A (p.Tyr3908Asn)
c.5869+5587T>A (n.5869+5587T>A)
2g.21005147A>CCA345977557APOBc.11721T>G (p.Asp3907Glu)
c.5869+5586T>G (n.5869+5586T>G)
2g.21005147A>GCA425136056APOBc.11721T>C (p.Asp3907=)
c.5869+5586T>C (n.5869+5586T>C)
 COSMIC
2g.21005147A>TCA345977558APOBc.11721T>A (p.Asp3907Glu)
c.5869+5586T>A (n.5869+5586T>A)
2g.21005148T>ACA345977562APOBc.11720A>T (p.Asp3907Val)
c.5869+5585A>T (n.5869+5585A>T)
2g.21005148T>CCA047187APOBc.11720A>G (p.Asp3907Gly)
c.5869+5585A>G (n.5869+5585A>G)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005148T>GCA345977560APOBc.11720A>C (p.Asp3907Ala)
c.5869+5585A>C (n.5869+5585A>C)
2g.21005148T=CA2493474271APOBc.11720A= (p.Asp3907=)
c.5869+5585A= (n.5869+5585A=)
2g.21005149C>ACA345977565APOBc.11719G>T (p.Asp3907Tyr)
c.5869+5584G>T (n.5869+5584G>T)
2g.21005149C=CA2493474272APOBc.11719G= (p.Asp3907=)
c.5869+5584G= (n.5869+5584G=)
2g.21005149C>GCA345977568APOBc.11719G>C (p.Asp3907His)
c.5869+5584G>C (n.5869+5584G>C)
2g.21005149C>TCA345977569APOBc.11719G>A (p.Asp3907Asn)
c.5869+5584G>A (n.5869+5584G>A)
 dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.21005150T>ACA425136057APOBc.11718A>T (p.Ala3906=)
c.5869+5583A>T (n.5869+5583A>T)
2g.21005150T>CCA425136058APOBc.11718A>G (p.Ala3906=)
c.5869+5583A>G (n.5869+5583A>G)
2g.21005150T>GCA425136059APOBc.11718A>C (p.Ala3906=)
c.5869+5583A>C (n.5869+5583A>C)
2g.21005151G>ACA345977572APOBc.11717C>T (p.Ala3906Val)
c.5869+5582C>T (n.5869+5582C>T)
2g.21005151G>CCA345977574APOBc.11717C>G (p.Ala3906Gly)
c.5869+5582C>G (n.5869+5582C>G)
 dbSNP
2g.21005151G=CA2493474273APOBc.11717C= (p.Ala3906=)
c.5869+5582C= (n.5869+5582C=)
2g.21005151G>TCA345977575APOBc.11717C>A (p.Ala3906Glu)
c.5869+5582C>A (n.5869+5582C>A)
2g.21005152C>ACA345977581APOBc.11716G>T (p.Ala3906Ser)
c.5869+5581G>T (n.5869+5581G>T)
2g.21005152C>GCA345977578APOBc.11716G>C (p.Ala3906Pro)
c.5869+5581G>C (n.5869+5581G>C)
2g.21005152C>TCA345977580APOBc.11716G>A (p.Ala3906Thr)
c.5869+5581G>A (n.5869+5581G>A)
2g.21005153T>ACA345977584APOBc.11715A>T (p.Lys3905Asn)
c.5869+5580A>T (n.5869+5580A>T)
2g.21005153T>CCA425136060APOBc.11715A>G (p.Lys3905=)
c.5869+5580A>G (n.5869+5580A>G)
2g.21005153T>GCA345977586APOBc.11715A>C (p.Lys3905Asn)
c.5869+5580A>C (n.5869+5580A>C)
2g.21005154T>ACA345977589APOBc.11714A>T (p.Lys3905Ile)
c.5869+5579A>T (n.5869+5579A>T)
2g.21005154T>CCA345977590APOBc.11714A>G (p.Lys3905Arg)
c.5869+5579A>G (n.5869+5579A>G)
 gnomAD v4
2g.21005154T>GCA345977592APOBc.11714A>C (p.Lys3905Thr)
c.5869+5579A>C (n.5869+5579A>C)
2g.21005155T>ACA345977595APOBc.11713A>T (p.Lys3905Ter)
c.5869+5578A>T (n.5869+5578A>T)
2g.21005155T>CCA345977598APOBc.11713A>G (p.Lys3905Glu)
c.5869+5578A>G (n.5869+5578A>G)
2g.21005155T>GCA345977596APOBc.11713A>C (p.Lys3905Gln)
c.5869+5578A>C (n.5869+5578A>C)
2g.21005155_21005156delinsTGCA2493474274APOBc.11712_11713delinsCA (p.Asn3904=)
c.5869+5577_5869+5578delinsCA (n.5869+5577_5869+5578delinsCA)
2g.21005156delCA022765APOBc.11712del (p.Asn3904LysfsTer21)
c.5869+5577del (n.5869+5577del)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21005156G>ACA425136061APOBc.11712C>T (p.Asn3904=)
c.5869+5577C>T (n.5869+5577C>T)
2g.21005156G>CCA345977601APOBc.11712C>G (p.Asn3904Lys)
c.5869+5577C>G (n.5869+5577C>G)
2g.21005156G>TCA345977602APOBc.11712C>A (p.Asn3904Lys)
c.5869+5577C>A (n.5869+5577C>A)
2g.21005157T>ACA345977607APOBc.11711A>T (p.Asn3904Ile)
c.5869+5576A>T (n.5869+5576A>T)
 dbSNP gnomAD v2
2g.21005157T>CCA345977609APOBc.11711A>G (p.Asn3904Ser)
c.5869+5576A>G (n.5869+5576A>G)
2g.21005157T>GCA345977610APOBc.11711A>C (p.Asn3904Thr)
c.5869+5576A>C (n.5869+5576A>C)
2g.21005157T=CA2493474275APOBc.11711A= (p.Asn3904=)
c.5869+5576A= (n.5869+5576A=)
2g.21005158T>ACA345977613APOBc.11710A>T (p.Asn3904Tyr)
c.5869+5575A>T (n.5869+5575A>T)
2g.21005158T>CCA345977615APOBc.11710A>G (p.Asn3904Asp)
c.5869+5575A>G (n.5869+5575A>G)
2g.21005158T>GCA345977617APOBc.11710A>C (p.Asn3904His)
c.5869+5575A>C (n.5869+5575A>C)
 COSMIC
2g.21005159T>ACA345977618APOBc.11709A>T (p.Lys3903Asn)
c.5869+5574A>T (n.5869+5574A>T)
2g.21005159T>CCA425136062APOBc.11709A>G (p.Lys3903=)
c.5869+5574A>G (n.5869+5574A>G)
2g.21005159T>GCA345977619APOBc.11709A>C (p.Lys3903Asn)
c.5869+5574A>C (n.5869+5574A>C)
2g.21005160T>ACA345977624APOBc.11708A>T (p.Lys3903Ile)
c.5869+5573A>T (n.5869+5573A>T)
2g.21005160T>CCA345977623APOBc.11708A>G (p.Lys3903Arg)
c.5869+5573A>G (n.5869+5573A>G)
2g.21005160T>GCA345977622APOBc.11708A>C (p.Lys3903Thr)
c.5869+5573A>C (n.5869+5573A>C)
2g.21005161T>ACA345977628APOBc.11707A>T (p.Lys3903Ter)
c.5869+5572A>T (n.5869+5572A>T)
 dbSNP
2g.21005161T>CCA345977629APOBc.11707A>G (p.Lys3903Glu)
c.5869+5572A>G (n.5869+5572A>G)
2g.21005161T>GCA345977631APOBc.11707A>C (p.Lys3903Gln)
c.5869+5572A>C (n.5869+5572A>C)
2g.21005161T=CA2493474276APOBc.11707A= (p.Lys3903=)
c.5869+5572A= (n.5869+5572A=)
2g.21005162C>ACA345977634APOBc.11706G>T (p.Leu3902Phe)
c.5869+5571G>T (n.5869+5571G>T)
2g.21005162C>GCA345977636APOBc.11706G>C (p.Leu3902Phe)
c.5869+5571G>C (n.5869+5571G>C)
2g.21005162C>TCA425136063APOBc.11706G>A (p.Leu3902=)
c.5869+5571G>A (n.5869+5571G>A)
2g.21005163A=CA2493474277APOBc.11705T= (p.Leu3902=)
c.5869+5570T= (n.5869+5570T=)
2g.21005163A>CCA345977639APOBc.11705T>G (p.Leu3902Trp)
c.5869+5570T>G (n.5869+5570T>G)
 dbSNP gnomAD v3 gnomAD v4
2g.21005163A>GCA345977640APOBc.11705T>C (p.Leu3902Ser)
c.5869+5570T>C (n.5869+5570T>C)
2g.21005163A>TCA345977642APOBc.11705T>A (p.Leu3902Ter)
c.5869+5570T>A (n.5869+5570T>A)
2g.21005164A>CCA345977644APOBc.11704T>G (p.Leu3902Val)
c.5869+5569T>G (n.5869+5569T>G)
2g.21005164A>GCA425136064APOBc.11704T>C (p.Leu3902=)
c.5869+5569T>C (n.5869+5569T>C)
2g.21005164A>TCA345977645APOBc.11704T>A (p.Leu3902Met)
c.5869+5569T>A (n.5869+5569T>A)
2g.21005165A>CCA345977647APOBc.11703T>G (p.Ser3901Arg)
c.5869+5568T>G (n.5869+5568T>G)
2g.21005165A>GCA425136065APOBc.11703T>C (p.Ser3901=)
c.5869+5568T>C (n.5869+5568T>C)
2g.21005165A>TCA345977648APOBc.11703T>A (p.Ser3901Arg)
c.5869+5568T>A (n.5869+5568T>A)
2g.21005166C>ACA345977650APOBc.11702G>T (p.Ser3901Ile)
c.5869+5567G>T (n.5869+5567G>T)
2g.21005166C=CA2493474278APOBc.11702G= (p.Ser3901=)
c.5869+5567G= (n.5869+5567G=)
2g.21005166C>GCA345977652APOBc.11702G>C (p.Ser3901Thr)
c.5869+5567G>C (n.5869+5567G>C)
 dbSNP gnomAD v2 gnomAD v4
2g.21005166C>TCA345977653APOBc.11702G>A (p.Ser3901Asn)
c.5869+5567G>A (n.5869+5567G>A)
2g.21005167T>ACA345977656APOBc.11701A>T (p.Ser3901Cys)
c.5869+5566A>T (n.5869+5566A>T)
2g.21005167T>CCA345977659APOBc.11701A>G (p.Ser3901Gly)
c.5869+5566A>G (n.5869+5566A>G)
 dbSNP
2g.21005167T>GCA345977658APOBc.11701A>C (p.Ser3901Arg)
c.5869+5566A>C (n.5869+5566A>C)
2g.21005167T=CA2493474279APOBc.11701A= (p.Ser3901=)
c.5869+5566A= (n.5869+5566A=)
2g.21005168G>ACA425136066APOBc.11700C>T (p.Ala3900=)
c.5869+5565C>T (n.5869+5565C>T)
 dbSNP
2g.21005168G>CCA425136067APOBc.11700C>G (p.Ala3900=)
c.5869+5565C>G (n.5869+5565C>G)
2g.21005168G=CA2493474280APOBc.11700C= (p.Ala3900=)
c.5869+5565C= (n.5869+5565C=)
2g.21005168G>TCA425136068APOBc.11700C>A (p.Ala3900=)
c.5869+5565C>A (n.5869+5565C>A)
2g.21005169G>ACA345977662APOBc.11699C>T (p.Ala3900Val)
c.5869+5564C>T (n.5869+5564C>T)
2g.21005169G>CCA345977663APOBc.11699C>G (p.Ala3900Gly)
c.5869+5564C>G (n.5869+5564C>G)
 dbSNP
2g.21005169G>TCA345977665APOBc.11699C>A (p.Ala3900Asp)
c.5869+5564C>A (n.5869+5564C>A)
 gnomAD v4
2g.21005170C>ACA345977668APOBc.11698G>T (p.Ala3900Ser)
c.5869+5563G>T (n.5869+5563G>T)
2g.21005170C>GCA345977669APOBc.11698G>C (p.Ala3900Pro)
c.5869+5563G>C (n.5869+5563G>C)
2g.21005170C>TCA345977671APOBc.11698G>A (p.Ala3900Thr)
c.5869+5563G>A (n.5869+5563G>A)
 COSMIC
2g.21005170_21005172delCA645535045APOBc.11696_11698del (p.Ser3899_Ala3900delinsThr)
c.5869+5561_5869+5563del (n.5869+5561_5869+5563del)
 COSMIC
2g.21005171A=CA2493474281APOBc.11697T= (p.Ser3899=)
c.5869+5562T= (n.5869+5562T=)
2g.21005171A>CCA345977674APOBc.11697T>G (p.Ser3899Arg)
c.5869+5562T>G (n.5869+5562T>G)
2g.21005171A>GCA425136069APOBc.11697T>C (p.Ser3899=)
c.5869+5562T>C (n.5869+5562T>C)
 dbSNP
2g.21005171A>TCA345977675APOBc.11697T>A (p.Ser3899Arg)
c.5869+5562T>A (n.5869+5562T>A)
 dbSNP gnomAD v2 gnomAD v4
2g.21005172C>ACA345977678APOBc.11696G>T (p.Ser3899Ile)
c.5869+5561G>T (n.5869+5561G>T)
 ClinVar
2g.21005172C=CA2493474282APOBc.11696G= (p.Ser3899=)
c.5869+5561G= (n.5869+5561G=)
2g.21005172C>GCA345977680APOBc.11696G>C (p.Ser3899Thr)
c.5869+5561G>C (n.5869+5561G>C)
2g.21005172C>TCA047165APOBc.11696G>A (p.Ser3899Asn)
c.5869+5561G>A (n.5869+5561G>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005173T>ACA345977684APOBc.11695A>T (p.Ser3899Cys)
c.5869+5560A>T (n.5869+5560A>T)
2g.21005173T>CCA345977687APOBc.11695A>G (p.Ser3899Gly)
c.5869+5560A>G (n.5869+5560A>G)
 gnomAD v4
2g.21005173T>GCA43491540APOBc.11695A>C (p.Ser3899Arg)
c.5869+5560A>C (n.5869+5560A>C)
 dbSNP
2g.21005173T=CA2493474283APOBc.11695A= (p.Ser3899=)
c.5869+5560A= (n.5869+5560A=)
2g.21005174C>ACA345977690APOBc.11694G>T (p.Trp3898Cys)
c.5869+5559G>T (n.5869+5559G>T)
2g.21005174C>GCA345977692APOBc.11694G>C (p.Trp3898Cys)
c.5869+5559G>C (n.5869+5559G>C)
2g.21005174C>TCA345977694APOBc.11694G>A (p.Trp3898Ter)
c.5869+5559G>A (n.5869+5559G>A)
 gnomAD v4
2g.21005175C>ACA345977697APOBc.11693G>T (p.Trp3898Leu)
c.5869+5558G>T (n.5869+5558G>T)
2g.21005175C>GCA345977698APOBc.11693G>C (p.Trp3898Ser)
c.5869+5558G>C (n.5869+5558G>C)
2g.21005175C>TCA345977700APOBc.11693G>A (p.Trp3898Ter)
c.5869+5558G>A (n.5869+5558G>A)
2g.21005176A>CCA345977702APOBc.11692T>G (p.Trp3898Gly)
c.5869+5557T>G (n.5869+5557T>G)
2g.21005176A>GCA345977703APOBc.11692T>C (p.Trp3898Arg)
c.5869+5557T>C (n.5869+5557T>C)
2g.21005176A>TCA345977705APOBc.11692T>A (p.Trp3898Arg)
c.5869+5557T>A (n.5869+5557T>A)
2g.21005177A=CA2493474284APOBc.11691T= (p.Thr3897=)
c.5869+5556T= (n.5869+5556T=)
2g.21005177A>CCA425136070APOBc.11691T>G (p.Thr3897=)
c.5869+5556T>G (n.5869+5556T>G)
 ClinVar dbSNP
2g.21005177A>GCA425136071APOBc.11691T>C (p.Thr3897=)
c.5869+5556T>C (n.5869+5556T>C)
 ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21005177A>TCA425136072APOBc.11691T>A (p.Thr3897=)
c.5869+5556T>A (n.5869+5556T>A)
2g.21005178G>ACA43491541APOBc.11690C>T (p.Thr3897Ile)
c.5869+5555C>T (n.5869+5555C>T)
 dbSNP gnomAD v4 COSMIC
2g.21005178G>CCA345977708APOBc.11690C>G (p.Thr3897Ser)
c.5869+5555C>G (n.5869+5555C>G)
2g.21005178G=CA2493474285APOBc.11690C= (p.Thr3897=)
c.5869+5555C= (n.5869+5555C=)
2g.21005178G>TCA345977710APOBc.11690C>A (p.Thr3897Asn)
c.5869+5555C>A (n.5869+5555C>A)
2g.21005179T>ACA345977716APOBc.11689A>T (p.Thr3897Ser)
c.5869+5554A>T (n.5869+5554A>T)
2g.21005179T>CCA345977712APOBc.11689A>G (p.Thr3897Ala)
c.5869+5554A>G (n.5869+5554A>G)
2g.21005179T>GCA345977714APOBc.11689A>C (p.Thr3897Pro)
c.5869+5554A>C (n.5869+5554A>C)
2g.21005180G>ACA425136074APOBc.11688C>T (p.Ala3896=)
c.5869+5553C>T (n.5869+5553C>T)
 dbSNP gnomAD v2 gnomAD v4
2g.21005180G>CCA425136075APOBc.11688C>G (p.Ala3896=)
c.5869+5553C>G (n.5869+5553C>G)
2g.21005180G=CA2493474286APOBc.11688C= (p.Ala3896=)
c.5869+5553C= (n.5869+5553C=)
2g.21005180G>TCA425136073APOBc.11688C>A (p.Ala3896=)
c.5869+5553C>A (n.5869+5553C>A)
2g.21005181G>ACA047153APOBc.11687C>T (p.Ala3896Val)
c.5869+5552C>T (n.5869+5552C>T)
 dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.21005181G>CCA345977719APOBc.11687C>G (p.Ala3896Gly)
c.5869+5552C>G (n.5869+5552C>G)
2g.21005181G=CA2493474287APOBc.11687C= (p.Ala3896=)
c.5869+5552C= (n.5869+5552C=)
2g.21005181G>TCA345977721APOBc.11687C>A (p.Ala3896Asp)
c.5869+5552C>A (n.5869+5552C>A)
 dbSNP gnomAD v3 gnomAD v4
2g.21005182C>ACA345977723APOBc.11686G>T (p.Ala3896Ser)
c.5869+5551G>T (n.5869+5551G>T)
 COSMIC
2g.21005182C>GCA345977725APOBc.11686G>C (p.Ala3896Pro)
c.5869+5551G>C (n.5869+5551G>C)
2g.21005182C>TCA345977727APOBc.11686G>A (p.Ala3896Thr)
c.5869+5551G>A (n.5869+5551G>A)
2g.21005183A=CA2493474288APOBc.11685T= (p.Asn3895=)
c.5869+5550T= (n.5869+5550T=)
2g.21005183A>CCA345977729APOBc.11685T>G (p.Asn3895Lys)
c.5869+5550T>G (n.5869+5550T>G)
2g.21005183A>GCA047140APOBc.11685T>C (p.Asn3895=)
c.5869+5550T>C (n.5869+5550T>C)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21005183A>TCA345977732APOBc.11685T>A (p.Asn3895Lys)
c.5869+5550T>A (n.5869+5550T>A)
 gnomAD v4
2g.21005184T>ACA345977735APOBc.11684A>T (p.Asn3895Ile)
c.5869+5549A>T (n.5869+5549A>T)
2g.21005184T>CCA345977736APOBc.11684A>G (p.Asn3895Ser)
c.5869+5549A>G (n.5869+5549A>G)
 dbSNP gnomAD v3 gnomAD v4
2g.21005184T>GCA345977737APOBc.11684A>C (p.Asn3895Thr)
c.5869+5549A>C (n.5869+5549A>C)
2g.21005184T=CA2493474289APOBc.11684A= (p.Asn3895=)
c.5869+5549A= (n.5869+5549A=)

Number of alleles fetched