Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21002618C>ACA345970452APOBc.12804G>T (p.Met4268Ile)
c.5870-3345G>T (n.5870-3345G>T)
2g.21002618C=CA2493473066APOBc.12804G= (p.Met4268=)
c.5870-3345G= (n.5870-3345G=)
2g.21002618C>GCA345970453APOBc.12804G>C (p.Met4268Ile)
c.5870-3345G>C (n.5870-3345G>C)
2g.21002618C>TCA051172APOBc.12804G>A (p.Met4268Ile)
c.5870-3345G>A (n.5870-3345G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002619A=CA2493473067APOBc.12803T= (p.Met4268=)
c.5870-3346T= (n.5870-3346T=)
2g.21002619A>CCA345970454APOBc.12803T>G (p.Met4268Arg)
c.5870-3346T>G (n.5870-3346T>G)
2g.21002619A>GCA051163APOBc.12803T>C (p.Met4268Thr)
c.5870-3346T>C (n.5870-3346T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002619A>TCA345970455APOBc.12803T>A (p.Met4268Lys)
c.5870-3346T>A (n.5870-3346T>A)
2g.21002620T>ACA345970456APOBc.12802A>T (p.Met4268Leu)
c.5870-3347A>T (n.5870-3347A>T)
2g.21002620T>CCA345970457APOBc.12802A>G (p.Met4268Val)
c.5870-3347A>G (n.5870-3347A>G)
gnomAD v4
2g.21002620T>GCA345970458APOBc.12802A>C (p.Met4268Leu)
c.5870-3347A>C (n.5870-3347A>C)
2g.21002621C>ACA425342504APOBc.12801G>T (p.Ser4267=)
c.5870-3348G>T (n.5870-3348G>T)
2g.21002621C=CA2493473068APOBc.12801G= (p.Ser4267=)
c.5870-3348G= (n.5870-3348G=)
2g.21002621C>GCA425342506APOBc.12801G>C (p.Ser4267=)
c.5870-3348G>C (n.5870-3348G>C)
2g.21002621C>TCA051148APOBc.12801G>A (p.Ser4267=)
c.5870-3348G>A (n.5870-3348G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002622G>ACA43488551APOBc.12800C>T (p.Ser4267Leu)
c.5870-3349C>T (n.5870-3349C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002622G>CCA345970460APOBc.12800C>G (p.Ser4267Trp)
c.5870-3349C>G (n.5870-3349C>G)
gnomAD v4
2g.21002622G=CA2493473069APOBc.12800C= (p.Ser4267=)
c.5870-3349C= (n.5870-3349C=)
2g.21002622G>TCA345970459APOBc.12800C>A (p.Ser4267Ter)
c.5870-3349C>A (n.5870-3349C>A)
2g.21002623A>CCA345970461APOBc.12799T>G (p.Ser4267Ala)
c.5870-3350T>G (n.5870-3350T>G)
2g.21002623A>GCA345970462APOBc.12799T>C (p.Ser4267Pro)
c.5870-3350T>C (n.5870-3350T>C)
2g.21002623A>TCA345970463APOBc.12799T>A (p.Ser4267Thr)
c.5870-3350T>A (n.5870-3350T>A)
2g.21002624G>ACA425342510APOBc.12798C>T (p.Ile4266=)
c.5870-3351C>T (n.5870-3351C>T)
dbSNP
2g.21002624G>CCA345970464APOBc.12798C>G (p.Ile4266Met)
c.5870-3351C>G (n.5870-3351C>G)
dbSNP COSMIC
2g.21002624G=CA2493473070APOBc.12798C= (p.Ile4266=)
c.5870-3351C= (n.5870-3351C=)
2g.21002624G>TCA425342511APOBc.12798C>A (p.Ile4266=)
c.5870-3351C>A (n.5870-3351C>A)
gnomAD v4 COSMIC
2g.21002625A>CCA345970465APOBc.12797T>G (p.Ile4266Ser)
c.5870-3352T>G (n.5870-3352T>G)
2g.21002625A>GCA345970466APOBc.12797T>C (p.Ile4266Thr)
c.5870-3352T>C (n.5870-3352T>C)
2g.21002625A>TCA345970467APOBc.12797T>A (p.Ile4266Asn)
c.5870-3352T>A (n.5870-3352T>A)
2g.21002625dupCA1546524APOBc.12797dup (p.Ser4267LeufsTer4)
c.5870-3352dup (n.5870-3352dup)
dbSNP ExAC gnomAD v2
2g.21002626T>ACA345970468APOBc.12796A>T (p.Ile4266Phe)
c.5870-3353A>T (n.5870-3353A>T)
2g.21002626T>CCA345970469APOBc.12796A>G (p.Ile4266Val)
c.5870-3353A>G (n.5870-3353A>G)
2g.21002626T>GCA345970470APOBc.12796A>C (p.Ile4266Leu)
c.5870-3353A>C (n.5870-3353A>C)
2g.21002627T>ACA425342225APOBc.12795A>T (p.Val4265=)
c.5870-3354A>T (n.5870-3354A>T)
2g.21002627T>CCA425342227APOBc.12795A>G (p.Val4265=)
c.5870-3354A>G (n.5870-3354A>G)
2g.21002627T>GCA425342228APOBc.12795A>C (p.Val4265=)
c.5870-3354A>C (n.5870-3354A>C)
2g.21002628A=CA2493473071APOBc.12794T= (p.Val4265=)
c.5870-3355T= (n.5870-3355T=)
2g.21002628A>CCA345970471APOBc.12794T>G (p.Val4265Gly)
c.5870-3355T>G (n.5870-3355T>G)
2g.21002628A>GCA051139APOBc.12794T>C (p.Val4265Ala)
c.5870-3355T>C (n.5870-3355T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002628A>TCA345970472APOBc.12794T>A (p.Val4265Glu)
c.5870-3355T>A (n.5870-3355T>A)
2g.21002629C>ACA345970473APOBc.12793G>T (p.Val4265Leu)
c.5870-3356G>T (n.5870-3356G>T)
2g.21002629C=CA2493473072APOBc.12793G= (p.Val4265=)
c.5870-3356G= (n.5870-3356G=)
2g.21002629C>GCA345970474APOBc.12793G>C (p.Val4265Leu)
c.5870-3356G>C (n.5870-3356G>C)
2g.21002629C>TCA051125APOBc.12793G>A (p.Val4265Ile)
c.5870-3356G>A (n.5870-3356G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002630A=CA2493473073APOBc.12792T= (p.Asp4264=)
c.5870-3357T= (n.5870-3357T=)
2g.21002630A>CCA345970475APOBc.12792T>G (p.Asp4264Glu)
c.5870-3357T>G (n.5870-3357T>G)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002630A>GCA425342235APOBc.12792T>C (p.Asp4264=)
c.5870-3357T>C (n.5870-3357T>C)
dbSNP gnomAD v3 gnomAD v4
2g.21002630A>TCA345970476APOBc.12792T>A (p.Asp4264Glu)
c.5870-3357T>A (n.5870-3357T>A)
COSMIC
2g.21002631T>ACA345970477APOBc.12791A>T (p.Asp4264Val)
c.5870-3358A>T (n.5870-3358A>T)
2g.21002631T>CCA345970478APOBc.12791A>G (p.Asp4264Gly)
c.5870-3358A>G (n.5870-3358A>G)
gnomAD v4
2g.21002631T>GCA345970479APOBc.12791A>C (p.Asp4264Ala)
c.5870-3358A>C (n.5870-3358A>C)
2g.21002632C>ACA345970480APOBc.12790G>T (p.Asp4264Tyr)
c.5870-3359G>T (n.5870-3359G>T)
2g.21002632C=CA2493473074APOBc.12790G= (p.Asp4264=)
c.5870-3359G= (n.5870-3359G=)
2g.21002632C>GCA345970481APOBc.12790G>C (p.Asp4264His)
c.5870-3359G>C (n.5870-3359G>C)
2g.21002632C>TCA051114APOBc.12790G>A (p.Asp4264Asn)
c.5870-3359G>A (n.5870-3359G>A)
dbSNP ExAC gnomAD v2 COSMIC
2g.21002633T>ACA425342240APOBc.12789A>T (p.Ile4263=)
c.5870-3360A>T (n.5870-3360A>T)
2g.21002633T>CCA345970482APOBc.12789A>G (p.Ile4263Met)
c.5870-3360A>G (n.5870-3360A>G)
2g.21002633T>GCA425342242APOBc.12789A>C (p.Ile4263=)
c.5870-3360A>C (n.5870-3360A>C)
2g.21002634A>CCA345970483APOBc.12788T>G (p.Ile4263Arg)
c.5870-3361T>G (n.5870-3361T>G)
2g.21002634A>GCA345970484APOBc.12788T>C (p.Ile4263Thr)
c.5870-3361T>C (n.5870-3361T>C)
2g.21002634A>TCA345970485APOBc.12788T>A (p.Ile4263Lys)
c.5870-3361T>A (n.5870-3361T>A)
2g.21002635T>ACA345970486APOBc.12787A>T (p.Ile4263Leu)
c.5870-3362A>T (n.5870-3362A>T)
2g.21002635T>CCA051098APOBc.12787A>G (p.Ile4263Val)
c.5870-3362A>G (n.5870-3362A>G)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002635T>GCA345970487APOBc.12787A>C (p.Ile4263Leu)
c.5870-3362A>C (n.5870-3362A>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21002635T=CA2493473075APOBc.12787A= (p.Ile4263=)
c.5870-3362A= (n.5870-3362A=)
2g.21002636delCA2658054431APOBc.12787del (p.Ile4263Ter)
c.5870-3362del (n.5870-3362del)
gnomAD v4
2g.21002636T>ACA425342245APOBc.12786A>T (p.Leu4262=)
c.5870-3363A>T (n.5870-3363A>T)
2g.21002636T>CCA425342246APOBc.12786A>G (p.Leu4262=)
c.5870-3363A>G (n.5870-3363A>G)
2g.21002636T>GCA425342248APOBc.12786A>C (p.Leu4262=)
c.5870-3363A>C (n.5870-3363A>C)
2g.21002637A>CCA345970490APOBc.12785T>G (p.Leu4262Arg)
c.5870-3364T>G (n.5870-3364T>G)
2g.21002637A>GCA345970488APOBc.12785T>C (p.Leu4262Pro)
c.5870-3364T>C (n.5870-3364T>C)
gnomAD v4
2g.21002637A>TCA345970489APOBc.12785T>A (p.Leu4262Gln)
c.5870-3364T>A (n.5870-3364T>A)
2g.21002638G>ACA051084APOBc.12784C>T (p.Leu4262=)
c.5870-3365C>T (n.5870-3365C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002638G>CCA345970491APOBc.12784C>G (p.Leu4262Val)
c.5870-3365C>G (n.5870-3365C>G)
2g.21002638G=CA2493473076APOBc.12784C= (p.Leu4262=)
c.5870-3365C= (n.5870-3365C=)
2g.21002638G>TCA345970492APOBc.12784C>A (p.Leu4262Ile)
c.5870-3365C>A (n.5870-3365C>A)
2g.21002639T>ACA345970493APOBc.12783A>T (p.Lys4261Asn)
c.5870-3366A>T (n.5870-3366A>T)
2g.21002639T>CCA425342253APOBc.12783A>G (p.Lys4261=)
c.5870-3366A>G (n.5870-3366A>G)
dbSNP gnomAD v4
2g.21002639T>GCA345970494APOBc.12783A>C (p.Lys4261Asn)
c.5870-3366A>C (n.5870-3366A>C)
2g.21002639T=CA2493473077APOBc.12783A= (p.Lys4261=)
c.5870-3366A= (n.5870-3366A=)
2g.21002640T>ACA345970495APOBc.12782A>T (p.Lys4261Ile)
c.5870-3367A>T (n.5870-3367A>T)
2g.21002640T>CCA345970496APOBc.12782A>G (p.Lys4261Arg)
c.5870-3367A>G (n.5870-3367A>G)
COSMIC
2g.21002640T>GCA345970497APOBc.12782A>C (p.Lys4261Thr)
c.5870-3367A>C (n.5870-3367A>C)
2g.21002641T>ACA345970498APOBc.12781A>T (p.Lys4261Ter)
c.5870-3368A>T (n.5870-3368A>T)
2g.21002641T>CCA345970499APOBc.12781A>G (p.Lys4261Glu)
c.5870-3368A>G (n.5870-3368A>G)
2g.21002641T>GCA345970500APOBc.12781A>C (p.Lys4261Gln)
c.5870-3368A>C (n.5870-3368A>C)
2g.21002642_21002643delCA2658054432APOBc.12780_12781del (p.His4260GlnfsTer10)
c.5870-3369_5870-3368del (n.5870-3369_5870-3368del)
gnomAD v4
2g.21002642A=CA2493473078APOBc.12780T= (p.His4260=)
c.5870-3369T= (n.5870-3369T=)
2g.21002642A>CCA345970501APOBc.12780T>G (p.His4260Gln)
c.5870-3369T>G (n.5870-3369T>G)
2g.21002642A>GCA425342259APOBc.12780T>C (p.His4260=)
c.5870-3369T>C (n.5870-3369T>C)
ClinVar dbSNP gnomAD v4
2g.21002642A>TCA345970502APOBc.12780T>A (p.His4260Gln)
c.5870-3369T>A (n.5870-3369T>A)
2g.21002643T>ACA345970503APOBc.12779A>T (p.His4260Leu)
c.5870-3370A>T (n.5870-3370A>T)
2g.21002643T>CCA051072APOBc.12779A>G (p.His4260Arg)
c.5870-3370A>G (n.5870-3370A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002643T>GCA345970504APOBc.12779A>C (p.His4260Pro)
c.5870-3370A>C (n.5870-3370A>C)
2g.21002643T=CA2493473079APOBc.12779A= (p.His4260=)
c.5870-3370A= (n.5870-3370A=)
2g.21002644G>ACA345970505APOBc.12778C>T (p.His4260Tyr)
c.5870-3371C>T (n.5870-3371C>T)
gnomAD v4
2g.21002644G>CCA345970506APOBc.12778C>G (p.His4260Asp)
c.5870-3371C>G (n.5870-3371C>G)
2g.21002644G>TCA345970507APOBc.12778C>A (p.His4260Asn)
c.5870-3371C>A (n.5870-3371C>A)
gnomAD v4
2g.21002645T>ACA345970508APOBc.12777A>T (p.Lys4259Asn)
c.5870-3372A>T (n.5870-3372A>T)
2g.21002645T>CCA425342263APOBc.12777A>G (p.Lys4259=)
c.5870-3372A>G (n.5870-3372A>G)
2g.21002645T>GCA345970509APOBc.12777A>C (p.Lys4259Asn)
c.5870-3372A>C (n.5870-3372A>C)
gnomAD v4
2g.21002646T>ACA345970510APOBc.12776A>T (p.Lys4259Ile)
c.5870-3373A>T (n.5870-3373A>T)
2g.21002646T>CCA345970511APOBc.12776A>G (p.Lys4259Arg)
c.5870-3373A>G (n.5870-3373A>G)
gnomAD v4
2g.21002646T>GCA345970512APOBc.12776A>C (p.Lys4259Thr)
c.5870-3373A>C (n.5870-3373A>C)
2g.21002647T>ACA345970513APOBc.12775A>T (p.Lys4259Ter)
c.5870-3374A>T (n.5870-3374A>T)
2g.21002647T>CCA345970514APOBc.12775A>G (p.Lys4259Glu)
c.5870-3374A>G (n.5870-3374A>G)
gnomAD v4
2g.21002647T>GCA345970515APOBc.12775A>C (p.Lys4259Gln)
c.5870-3374A>C (n.5870-3374A>C)
2g.21002648C>ACA345970516APOBc.12774G>T (p.Arg4258Ser)
c.5870-3375G>T (n.5870-3375G>T)
2g.21002648C>GCA345970517APOBc.12774G>C (p.Arg4258Ser)
c.5870-3375G>C (n.5870-3375G>C)
2g.21002648C>TCA425342270APOBc.12774G>A (p.Arg4258=)
c.5870-3375G>A (n.5870-3375G>A)
COSMIC
2g.21002649C>ACA345970519APOBc.12773G>T (p.Arg4258Met)
c.5870-3376G>T (n.5870-3376G>T)
2g.21002649C=CA2493473080APOBc.12773G= (p.Arg4258=)
c.5870-3376G= (n.5870-3376G=)
2g.21002649C>GCA345970518APOBc.12773G>C (p.Arg4258Thr)
c.5870-3376G>C (n.5870-3376G>C)
2g.21002649C>TCA051062APOBc.12773G>A (p.Arg4258Lys)
c.5870-3376G>A (n.5870-3376G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002650T>ACA345970520APOBc.12772A>T (p.Arg4258Trp)
c.5870-3377A>T (n.5870-3377A>T)
2g.21002650T>CCA345970521APOBc.12772A>G (p.Arg4258Gly)
c.5870-3377A>G (n.5870-3377A>G)
2g.21002650T>GCA425342273APOBc.12772A>C (p.Arg4258=)
c.5870-3377A>C (n.5870-3377A>C)
2g.21002651T>ACA345970522APOBc.12771A>T (p.Leu4257Phe)
c.5870-3378A>T (n.5870-3378A>T)
2g.21002651T>CCA425342277APOBc.12771A>G (p.Leu4257=)
c.5870-3378A>G (n.5870-3378A>G)
2g.21002651T>GCA345970523APOBc.12771A>C (p.Leu4257Phe)
c.5870-3378A>C (n.5870-3378A>C)
2g.21002652A=CA2493473081APOBc.12770T= (p.Leu4257=)
c.5870-3379T= (n.5870-3379T=)
2g.21002652A>CCA345970524APOBc.12770T>G (p.Leu4257Ter)
c.5870-3379T>G (n.5870-3379T>G)
2g.21002652A>GCA051046APOBc.12770T>C (p.Leu4257Ser)
c.5870-3379T>C (n.5870-3379T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002652A>TCA345970525APOBc.12770T>A (p.Leu4257Ter)
c.5870-3379T>A (n.5870-3379T>A)
2g.21002653A>CCA345970526APOBc.12769T>G (p.Leu4257Val)
c.5870-3380T>G (n.5870-3380T>G)
gnomAD v4
2g.21002653A>GCA425342280APOBc.12769T>C (p.Leu4257=)
c.5870-3380T>C (n.5870-3380T>C)
2g.21002653A>TCA345970527APOBc.12769T>A (p.Leu4257Ile)
c.5870-3380T>A (n.5870-3380T>A)
2g.21002654C>ACA345970528APOBc.12768G>T (p.Glu4256Asp)
c.5870-3381G>T (n.5870-3381G>T)
2g.21002654C=CA2493473082APOBc.12768G= (p.Glu4256=)
c.5870-3381G= (n.5870-3381G=)
2g.21002654C>GCA345970529APOBc.12768G>C (p.Glu4256Asp)
c.5870-3381G>C (n.5870-3381G>C)
2g.21002654C>TCA43488597APOBc.12768G>A (p.Glu4256=)
c.5870-3381G>A (n.5870-3381G>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21002655T>ACA345970530APOBc.12767A>T (p.Glu4256Val)
c.5870-3382A>T (n.5870-3382A>T)
2g.21002655T>CCA345970532APOBc.12767A>G (p.Glu4256Gly)
c.5870-3382A>G (n.5870-3382A>G)
gnomAD v4
2g.21002655T>GCA345970531APOBc.12767A>C (p.Glu4256Ala)
c.5870-3382A>C (n.5870-3382A>C)
2g.21002656C>ACA43488609APOBc.12766G>T (p.Glu4256Ter)
c.5870-3383G>T (n.5870-3383G>T)
dbSNP
2g.21002656C=CA2493473083APOBc.12766G= (p.Glu4256=)
c.5870-3383G= (n.5870-3383G=)
2g.21002656C>GCA43488612APOBc.12766G>C (p.Glu4256Gln)
c.5870-3383G>C (n.5870-3383G>C)
ClinVar
2g.21002656C>TCA051037APOBc.12766G>A (p.Glu4256Lys)
c.5870-3383G>A (n.5870-3383G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21002657G>ACA051028APOBc.12765C>T (p.Phe4255=)
c.5870-3384C>T (n.5870-3384C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002657G>CCA345970534APOBc.12765C>G (p.Phe4255Leu)
c.5870-3384C>G (n.5870-3384C>G)
2g.21002657G=CA2493473084APOBc.12765C= (p.Phe4255=)
c.5870-3384C= (n.5870-3384C=)
2g.21002657G>TCA345970533APOBc.12765C>A (p.Phe4255Leu)
c.5870-3384C>A (n.5870-3384C>A)
dbSNP gnomAD v3 gnomAD v4
2g.21002658A>CCA345970535APOBc.12764T>G (p.Phe4255Cys)
c.5870-3385T>G (n.5870-3385T>G)
2g.21002658A>GCA345970536APOBc.12764T>C (p.Phe4255Ser)
c.5870-3385T>C (n.5870-3385T>C)
2g.21002658A>TCA345970537APOBc.12764T>A (p.Phe4255Tyr)
c.5870-3385T>A (n.5870-3385T>A)
2g.21002659A>CCA345970538APOBc.12763T>G (p.Phe4255Val)
c.5870-3386T>G (n.5870-3386T>G)
2g.21002659A>GCA345970539APOBc.12763T>C (p.Phe4255Leu)
c.5870-3386T>C (n.5870-3386T>C)
2g.21002659A>TCA345970540APOBc.12763T>A (p.Phe4255Ile)
c.5870-3386T>A (n.5870-3386T>A)
2g.21002660A>CCA425342287APOBc.12762T>G (p.Pro4254=)
c.5870-3387T>G (n.5870-3387T>G)
2g.21002660A>GCA425342289APOBc.12762T>C (p.Pro4254=)
c.5870-3387T>C (n.5870-3387T>C)
2g.21002660A>TCA425342291APOBc.12762T>A (p.Pro4254=)
c.5870-3387T>A (n.5870-3387T>A)
2g.21002661G>ACA051018APOBc.12761C>T (p.Pro4254Leu)
c.5870-3388C>T (n.5870-3388C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002661G>CCA345970541APOBc.12761C>G (p.Pro4254Arg)
c.5870-3388C>G (n.5870-3388C>G)
2g.21002661G=CA2493473085APOBc.12761C= (p.Pro4254=)
c.5870-3388C= (n.5870-3388C=)
2g.21002661G>TCA345970542APOBc.12761C>A (p.Pro4254His)
c.5870-3388C>A (n.5870-3388C>A)
2g.21002662G>ACA345970543APOBc.12760C>T (p.Pro4254Ser)
c.5870-3389C>T (n.5870-3389C>T)
gnomAD v4 COSMIC
2g.21002662G>CCA345970544APOBc.12760C>G (p.Pro4254Ala)
c.5870-3389C>G (n.5870-3389C>G)
2g.21002662G>TCA345970545APOBc.12760C>A (p.Pro4254Thr)
c.5870-3389C>A (n.5870-3389C>A)
2g.21002663A>CCA425342301APOBc.12759T>G (p.Leu4253=)
c.5870-3390T>G (n.5870-3390T>G)
2g.21002663A>GCA425342299APOBc.12759T>C (p.Leu4253=)
c.5870-3390T>C (n.5870-3390T>C)
2g.21002663A>TCA425342300APOBc.12759T>A (p.Leu4253=)
c.5870-3390T>A (n.5870-3390T>A)
2g.21002664A=CA2493473086APOBc.12758T= (p.Leu4253=)
c.5870-3391T= (n.5870-3391T=)
2g.21002664A>CCA345970547APOBc.12758T>G (p.Leu4253Arg)
c.5870-3391T>G (n.5870-3391T>G)
2g.21002664A>GCA051009APOBc.12758T>C (p.Leu4253Pro)
c.5870-3391T>C (n.5870-3391T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002664A>TCA345970546APOBc.12758T>A (p.Leu4253His)
c.5870-3391T>A (n.5870-3391T>A)
2g.21002665G>ACA345970548APOBc.12757C>T (p.Leu4253Phe)
c.5870-3392C>T (n.5870-3392C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002665G>CCA345970549APOBc.12757C>G (p.Leu4253Val)
c.5870-3392C>G (n.5870-3392C>G)
2g.21002665G=CA2493473087APOBc.12757C= (p.Leu4253=)
c.5870-3392C= (n.5870-3392C=)
2g.21002665G>TCA345970550APOBc.12757C>A (p.Leu4253Ile)
c.5870-3392C>A (n.5870-3392C>A)
2g.21002666T>ACA425342305APOBc.12756A>T (p.Thr4252=)
c.5870-3393A>T (n.5870-3393A>T)
2g.21002666T>CCA425342306APOBc.12756A>G (p.Thr4252=)
c.5870-3393A>G (n.5870-3393A>G)
dbSNP gnomAD v4
2g.21002666T>GCA425342307APOBc.12756A>C (p.Thr4252=)
c.5870-3393A>C (n.5870-3393A>C)
2g.21002666T=CA2493473088APOBc.12756A= (p.Thr4252=)
c.5870-3393A= (n.5870-3393A=)
2g.21002667G>ACA345970551APOBc.12755C>T (p.Thr4252Ile)
c.5870-3394C>T (n.5870-3394C>T)
2g.21002667G>CCA345970552APOBc.12755C>G (p.Thr4252Arg)
c.5870-3394C>G (n.5870-3394C>G)
2g.21002667G>TCA345970553APOBc.12755C>A (p.Thr4252Lys)
c.5870-3394C>A (n.5870-3394C>A)
2g.21002668T>ACA345970554APOBc.12754A>T (p.Thr4252Ser)
c.5870-3395A>T (n.5870-3395A>T)
2g.21002668T>CCA345970555APOBc.12754A>G (p.Thr4252Ala)
c.5870-3395A>G (n.5870-3395A>G)
2g.21002668T>GCA345970556APOBc.12754A>C (p.Thr4252Pro)
c.5870-3395A>C (n.5870-3395A>C)
2g.21002669A>CCA345970557APOBc.12753T>G (p.Ile4251Met)
c.5870-3396T>G (n.5870-3396T>G)
2g.21002669A>GCA425342312APOBc.12753T>C (p.Ile4251=)
c.5870-3396T>C (n.5870-3396T>C)
2g.21002669A>TCA425342313APOBc.12753T>A (p.Ile4251=)
c.5870-3396T>A (n.5870-3396T>A)
2g.21002670A>CCA345970560APOBc.12752T>G (p.Ile4251Ser)
c.5870-3397T>G (n.5870-3397T>G)
2g.21002670A>GCA345970559APOBc.12752T>C (p.Ile4251Thr)
c.5870-3397T>C (n.5870-3397T>C)
gnomAD v4
2g.21002670A>TCA345970558APOBc.12752T>A (p.Ile4251Asn)
c.5870-3397T>A (n.5870-3397T>A)
2g.21002671T>ACA345970561APOBc.12751A>T (p.Ile4251Phe)
c.5870-3398A>T (n.5870-3398A>T)
2g.21002671T>CCA050994APOBc.12751A>G (p.Ile4251Val)
c.5870-3398A>G (n.5870-3398A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002671T>GCA345970562APOBc.12751A>C (p.Ile4251Leu)
c.5870-3398A>C (n.5870-3398A>C)
2g.21002671T=CA2493473089APOBc.12751A= (p.Ile4251=)
c.5870-3398A= (n.5870-3398A=)
2g.21002672C>ACA425342318APOBc.12750G>T (p.Val4250=)
c.5870-3399G>T (n.5870-3399G>T)
2g.21002672C>GCA425342319APOBc.12750G>C (p.Val4250=)
c.5870-3399G>C (n.5870-3399G>C)
2g.21002672C>TCA425342320APOBc.12750G>A (p.Val4250=)
c.5870-3399G>A (n.5870-3399G>A)
gnomAD v4
2g.21002673A>CCA345970563APOBc.12749T>G (p.Val4250Gly)
c.5870-3400T>G (n.5870-3400T>G)
2g.21002673A>GCA345970564APOBc.12749T>C (p.Val4250Ala)
c.5870-3400T>C (n.5870-3400T>C)
2g.21002673A>TCA345970565APOBc.12749T>A (p.Val4250Glu)
c.5870-3400T>A (n.5870-3400T>A)
2g.21002674C>ACA345970566APOBc.12748G>T (p.Val4250Leu)
c.5870-3401G>T (n.5870-3401G>T)
2g.21002674C>GCA345970567APOBc.12748G>C (p.Val4250Leu)
c.5870-3401G>C (n.5870-3401G>C)
2g.21002674C>TCA345970568APOBc.12748G>A (p.Val4250Met)
c.5870-3401G>A (n.5870-3401G>A)
2g.21002675T>ACA425342325APOBc.12747A>T (p.Leu4249=)
c.5870-3402A>T (n.5870-3402A>T)
2g.21002675T>CCA425342326APOBc.12747A>G (p.Leu4249=)
c.5870-3402A>G (n.5870-3402A>G)
2g.21002675T>GCA425342327APOBc.12747A>C (p.Leu4249=)
c.5870-3402A>C (n.5870-3402A>C)
2g.21002676delCA2658054433APOBc.12746del (p.Leu4249GlnfsTer2)
c.5870-3403del (n.5870-3403del)
gnomAD v4
2g.21002676A=CA2493473090APOBc.12746T= (p.Leu4249=)
c.5870-3403T= (n.5870-3403T=)
2g.21002676A>CCA345970569APOBc.12746T>G (p.Leu4249Arg)
c.5870-3403T>G (n.5870-3403T>G)
2g.21002676A>GCA43488642APOBc.12746T>C (p.Leu4249Pro)
c.5870-3403T>C (n.5870-3403T>C)
dbSNP
2g.21002676A>TCA345970570APOBc.12746T>A (p.Leu4249Gln)
c.5870-3403T>A (n.5870-3403T>A)
2g.21002677G>ACA425342332APOBc.12745C>T (p.Leu4249=)
c.5870-3404C>T (n.5870-3404C>T)
gnomAD v4
2g.21002677G>CCA345970571APOBc.12745C>G (p.Leu4249Val)
c.5870-3404C>G (n.5870-3404C>G)
2g.21002677G>TCA345970572APOBc.12745C>A (p.Leu4249Ile)
c.5870-3404C>A (n.5870-3404C>A)
gnomAD v4
2g.21002678G>ACA425342335APOBc.12744C>T (p.Asp4248=)
c.5870-3405C>T (n.5870-3405C>T)
ClinVar dbSNP
2g.21002678G>CCA345970573APOBc.12744C>G (p.Asp4248Glu)
c.5870-3405C>G (n.5870-3405C>G)
2g.21002678G=CA2493473091APOBc.12744C= (p.Asp4248=)
c.5870-3405C= (n.5870-3405C=)
2g.21002678G>TCA345970574APOBc.12744C>A (p.Asp4248Glu)
c.5870-3405C>A (n.5870-3405C>A)
2g.21002679T>ACA345970575APOBc.12743A>T (p.Asp4248Val)
c.5870-3406A>T (n.5870-3406A>T)
2g.21002679T>CCA345970576APOBc.12743A>G (p.Asp4248Gly)
c.5870-3406A>G (n.5870-3406A>G)
gnomAD v4
2g.21002679T>GCA345970577APOBc.12743A>C (p.Asp4248Ala)
c.5870-3406A>C (n.5870-3406A>C)
2g.21002680C>ACA345970578APOBc.12742G>T (p.Asp4248Tyr)
c.5870-3407G>T (n.5870-3407G>T)
2g.21002680C=CA2493473092APOBc.12742G= (p.Asp4248=)
c.5870-3407G= (n.5870-3407G=)
2g.21002680C>GCA345970579APOBc.12742G>C (p.Asp4248His)
c.5870-3407G>C (n.5870-3407G>C)
2g.21002680C>TCA345970580APOBc.12742G>A (p.Asp4248Asn)
c.5870-3407G>A (n.5870-3407G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21002681T>ACA345970581APOBc.12741A>T (p.Gln4247His)
c.5870-3408A>T (n.5870-3408A>T)
2g.21002681T>CCA425342340APOBc.12741A>G (p.Gln4247=)
c.5870-3408A>G (n.5870-3408A>G)
dbSNP gnomAD v4
2g.21002681T>GCA345970582APOBc.12741A>C (p.Gln4247His)
c.5870-3408A>C (n.5870-3408A>C)
COSMIC
2g.21002681T=CA2493473093APOBc.12741A= (p.Gln4247=)
c.5870-3408A= (n.5870-3408A=)
2g.21002682T>ACA345970583APOBc.12740A>T (p.Gln4247Leu)
c.5870-3409A>T (n.5870-3409A>T)
2g.21002682T>CCA345970584APOBc.12740A>G (p.Gln4247Arg)
c.5870-3409A>G (n.5870-3409A>G)
2g.21002682T>GCA345970585APOBc.12740A>C (p.Gln4247Pro)
c.5870-3409A>C (n.5870-3409A>C)
2g.21002683G>ACA43488656APOBc.12739C>T (p.Gln4247Ter)
c.5870-3410C>T (n.5870-3410C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002683G>CCA345970587APOBc.12739C>G (p.Gln4247Glu)
c.5870-3410C>G (n.5870-3410C>G)
2g.21002683G=CA2493473094APOBc.12739C= (p.Gln4247=)
c.5870-3410C= (n.5870-3410C=)
2g.21002683G>TCA345970586APOBc.12739C>A (p.Gln4247Lys)
c.5870-3410C>A (n.5870-3410C>A)
2g.21002684G>ACA425342346APOBc.12738C>T (p.Phe4246=)
c.5870-3411C>T (n.5870-3411C>T)
gnomAD v4 COSMIC
2g.21002684G>CCA345970588APOBc.12738C>G (p.Phe4246Leu)
c.5870-3411C>G (n.5870-3411C>G)
2g.21002684G>TCA345970589APOBc.12738C>A (p.Phe4246Leu)
c.5870-3411C>A (n.5870-3411C>A)
2g.21002685A>CCA345970590APOBc.12737T>G (p.Phe4246Cys)
c.5870-3412T>G (n.5870-3412T>G)
2g.21002685A>GCA345970591APOBc.12737T>C (p.Phe4246Ser)
c.5870-3412T>C (n.5870-3412T>C)
2g.21002685A>TCA345970592APOBc.12737T>A (p.Phe4246Tyr)
c.5870-3412T>A (n.5870-3412T>A)
2g.21002686A=CA2493473095APOBc.12736T= (p.Phe4246=)
c.5870-3413T= (n.5870-3413T=)
2g.21002686A>CCA050982APOBc.12736T>G (p.Phe4246Val)
c.5870-3413T>G (n.5870-3413T>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002686A>GCA345970593APOBc.12736T>C (p.Phe4246Leu)
c.5870-3413T>C (n.5870-3413T>C)
2g.21002686A>TCA345970594APOBc.12736T>A (p.Phe4246Ile)
c.5870-3413T>A (n.5870-3413T>A)
gnomAD v4
2g.21002687A>CCA345970595APOBc.12735T>G (p.Tyr4245Ter)
c.5870-3414T>G (n.5870-3414T>G)
2g.21002687A>GCA425342353APOBc.12735T>C (p.Tyr4245=)
c.5870-3414T>C (n.5870-3414T>C)
2g.21002687A>TCA345970596APOBc.12735T>A (p.Tyr4245Ter)
c.5870-3414T>A (n.5870-3414T>A)
2g.21002688T>ACA345970597APOBc.12734A>T (p.Tyr4245Phe)
c.5870-3415A>T (n.5870-3415A>T)
2g.21002688T>CCA345970598APOBc.12734A>G (p.Tyr4245Cys)
c.5870-3415A>G (n.5870-3415A>G)
2g.21002688T>GCA050973APOBc.12734A>C (p.Tyr4245Ser)
c.5870-3415A>C (n.5870-3415A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002688T=CA2493473096APOBc.12734A= (p.Tyr4245=)
c.5870-3415A= (n.5870-3415A=)
2g.21002689A>CCA345970601APOBc.12733T>G (p.Tyr4245Asp)
c.5870-3416T>G (n.5870-3416T>G)
2g.21002689A>GCA345970600APOBc.12733T>C (p.Tyr4245His)
c.5870-3416T>C (n.5870-3416T>C)
2g.21002689A>TCA345970599APOBc.12733T>A (p.Tyr4245Asn)
c.5870-3416T>A (n.5870-3416T>A)
2g.21002690G>ACA425342368APOBc.12732C>T (p.Ser4244=)
c.5870-3417C>T (n.5870-3417C>T)
ClinVar dbSNP gnomAD v4
2g.21002690G>CCA425342370APOBc.12732C>G (p.Ser4244=)
c.5870-3417C>G (n.5870-3417C>G)
2g.21002690G=CA2493473097APOBc.12732C= (p.Ser4244=)
c.5870-3417C= (n.5870-3417C=)
2g.21002690G>TCA425342369APOBc.12732C>A (p.Ser4244=)
c.5870-3417C>A (n.5870-3417C>A)
2g.21002691G>ACA345970602APOBc.12731C>T (p.Ser4244Phe)
c.5870-3418C>T (n.5870-3418C>T)
gnomAD v4 COSMIC
2g.21002691G>CCA43488680APOBc.12731C>G (p.Ser4244Cys)
c.5870-3418C>G (n.5870-3418C>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002691G=CA2493473098APOBc.12731C= (p.Ser4244=)
c.5870-3418C= (n.5870-3418C=)
2g.21002691G>TCA345970603APOBc.12731C>A (p.Ser4244Tyr)
c.5870-3418C>A (n.5870-3418C>A)
2g.21002692A>CCA345970604APOBc.12730T>G (p.Ser4244Ala)
c.5870-3419T>G (n.5870-3419T>G)
2g.21002692A>GCA345970605APOBc.12730T>C (p.Ser4244Pro)
c.5870-3419T>C (n.5870-3419T>C)
ClinVar dbSNP gnomAD v4
2g.21002692A>TCA345970606APOBc.12730T>A (p.Ser4244Thr)
c.5870-3419T>A (n.5870-3419T>A)
2g.21002693A>CCA345970607APOBc.12729T>G (p.Phe4243Leu)
c.5870-3420T>G (n.5870-3420T>G)
2g.21002693A>GCA425342374APOBc.12729T>C (p.Phe4243=)
c.5870-3420T>C (n.5870-3420T>C)
2g.21002693A>TCA345970608APOBc.12729T>A (p.Phe4243Leu)
c.5870-3420T>A (n.5870-3420T>A)
2g.21002694A>CCA345970609APOBc.12728T>G (p.Phe4243Cys)
c.5870-3421T>G (n.5870-3421T>G)
ClinVar gnomAD v4 COSMIC
2g.21002694A>GCA345970610APOBc.12728T>C (p.Phe4243Ser)
c.5870-3421T>C (n.5870-3421T>C)
2g.21002694A>TCA345970611APOBc.12728T>A (p.Phe4243Tyr)
c.5870-3421T>A (n.5870-3421T>A)
gnomAD v4
2g.21002695A=CA2493473099APOBc.12727T= (p.Phe4243=)
c.5870-3422T= (n.5870-3422T=)
2g.21002695A>CCA345970612APOBc.12727T>G (p.Phe4243Val)
c.5870-3422T>G (n.5870-3422T>G)
2g.21002695A>GCA345970613APOBc.12727T>C (p.Phe4243Leu)
c.5870-3422T>C (n.5870-3422T>C)
dbSNP
2g.21002695A>TCA345970614APOBc.12727T>A (p.Phe4243Ile)
c.5870-3422T>A (n.5870-3422T>A)
2g.21002696C>ACA425342379APOBc.12726G>T (p.Leu4242=)
c.5870-3423G>T (n.5870-3423G>T)
2g.21002696C>GCA425342380APOBc.12726G>C (p.Leu4242=)
c.5870-3423G>C (n.5870-3423G>C)
2g.21002696C>TCA425342381APOBc.12726G>A (p.Leu4242=)
c.5870-3423G>A (n.5870-3423G>A)
2g.21002697A>CCA345970616APOBc.12725T>G (p.Leu4242Arg)
c.5870-3424T>G (n.5870-3424T>G)
2g.21002697A>GCA345970617APOBc.12725T>C (p.Leu4242Pro)
c.5870-3424T>C (n.5870-3424T>C)
2g.21002697A>TCA345970615APOBc.12725T>A (p.Leu4242Gln)
c.5870-3424T>A (n.5870-3424T>A)
2g.21002698G>ACA425342383APOBc.12724C>T (p.Leu4242=)
c.5870-3425C>T (n.5870-3425C>T)
dbSNP
2g.21002698G>CCA345970618APOBc.12724C>G (p.Leu4242Val)
c.5870-3425C>G (n.5870-3425C>G)
gnomAD v4
2g.21002698G=CA2493473100APOBc.12724C= (p.Leu4242=)
c.5870-3425C= (n.5870-3425C=)
2g.21002698G>TCA050957APOBc.12724C>A (p.Leu4242Met)
c.5870-3425C>A (n.5870-3425C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002699T>ACA43488681APOBc.12723A>T (p.Ile4241=)
c.5870-3426A>T (n.5870-3426A>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002699T>CCA345970619APOBc.12723A>G (p.Ile4241Met)
c.5870-3426A>G (n.5870-3426A>G)
2g.21002699T>GCA425342387APOBc.12723A>C (p.Ile4241=)
c.5870-3426A>C (n.5870-3426A>C)
2g.21002699T=CA2493473101APOBc.12723A= (p.Ile4241=)
c.5870-3426A= (n.5870-3426A=)
2g.21002700A=CA2493473102APOBc.12722T= (p.Ile4241=)
c.5870-3427T= (n.5870-3427T=)
2g.21002700A>CCA345970620APOBc.12722T>G (p.Ile4241Arg)
c.5870-3427T>G (n.5870-3427T>G)
2g.21002700A>GCA43488686APOBc.12722T>C (p.Ile4241Thr)
c.5870-3427T>C (n.5870-3427T>C)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21002700A>TCA345970621APOBc.12722T>A (p.Ile4241Lys)
c.5870-3427T>A (n.5870-3427T>A)
2g.21002701T>ACA345970622APOBc.12721A>T (p.Ile4241Leu)
c.5870-3428A>T (n.5870-3428A>T)
2g.21002701T>CCA345970623APOBc.12721A>G (p.Ile4241Val)
c.5870-3428A>G (n.5870-3428A>G)
2g.21002701T>GCA345970624APOBc.12721A>C (p.Ile4241Leu)
c.5870-3428A>C (n.5870-3428A>C)
2g.21002702T>ACA345970625APOBc.12720A>T (p.Glu4240Asp)
c.5870-3429A>T (n.5870-3429A>T)
2g.21002702T>CCA425342392APOBc.12720A>G (p.Glu4240=)
c.5870-3429A>G (n.5870-3429A>G)
2g.21002702T>GCA345970626APOBc.12720A>C (p.Glu4240Asp)
c.5870-3429A>C (n.5870-3429A>C)
2g.21002703T>ACA345970629APOBc.12719A>T (p.Glu4240Val)
c.5870-3430A>T (n.5870-3430A>T)
2g.21002703T>CCA345970628APOBc.12719A>G (p.Glu4240Gly)
c.5870-3430A>G (n.5870-3430A>G)
2g.21002703T>GCA345970627APOBc.12719A>C (p.Glu4240Ala)
c.5870-3430A>C (n.5870-3430A>C)
2g.21002704C>ACA345970630APOBc.12718G>T (p.Glu4240Ter)
c.5870-3431G>T (n.5870-3431G>T)
2g.21002704C>GCA345970631APOBc.12718G>C (p.Glu4240Gln)
c.5870-3431G>C (n.5870-3431G>C)
2g.21002704C>TCA345970632APOBc.12718G>A (p.Glu4240Lys)
c.5870-3431G>A (n.5870-3431G>A)
2g.21002705T>ACA425342396APOBc.12717A>T (p.Ser4239=)
c.5870-3432A>T (n.5870-3432A>T)
2g.21002705T>CCA425342397APOBc.12717A>G (p.Ser4239=)
c.5870-3432A>G (n.5870-3432A>G)
2g.21002705T>GCA425342398APOBc.12717A>C (p.Ser4239=)
c.5870-3432A>C (n.5870-3432A>C)
2g.21002706G>ACA345970633APOBc.12716C>T (p.Ser4239Leu)
c.5870-3433C>T (n.5870-3433C>T)
2g.21002706G>CCA345970634APOBc.12716C>G (p.Ser4239Ter)
c.5870-3433C>G (n.5870-3433C>G)
2g.21002706G>TCA345970635APOBc.12716C>A (p.Ser4239Ter)
c.5870-3433C>A (n.5870-3433C>A)
2g.21002707A=CA2493473103APOBc.12715T= (p.Ser4239=)
c.5870-3434T= (n.5870-3434T=)
2g.21002707A>CCA345970636APOBc.12715T>G (p.Ser4239Ala)
c.5870-3434T>G (n.5870-3434T>G)
2g.21002707A>GCA050948APOBc.12715T>C (p.Ser4239Pro)
c.5870-3434T>C (n.5870-3434T>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21002707A>TCA345970637APOBc.12715T>A (p.Ser4239Thr)
c.5870-3434T>A (n.5870-3434T>A)
2g.21002708A>CCA425342402APOBc.12714T>G (p.Gly4238=)
c.5870-3435T>G (n.5870-3435T>G)
gnomAD v4
2g.21002708A>GCA425342403APOBc.12714T>C (p.Gly4238=)
c.5870-3435T>C (n.5870-3435T>C)
2g.21002708A>TCA425342404APOBc.12714T>A (p.Gly4238=)
c.5870-3435T>A (n.5870-3435T>A)
2g.21002709C>ACA345970638APOBc.12713G>T (p.Gly4238Val)
c.5870-3436G>T (n.5870-3436G>T)
2g.21002709C>GCA345970639APOBc.12713G>C (p.Gly4238Ala)
c.5870-3436G>C (n.5870-3436G>C)
2g.21002709C>TCA345970640APOBc.12713G>A (p.Gly4238Asp)
c.5870-3436G>A (n.5870-3436G>A)
2g.21002710C>ACA345970641APOBc.12712G>T (p.Gly4238Cys)
c.5870-3437G>T (n.5870-3437G>T)
2g.21002710C>GCA345970643APOBc.12712G>C (p.Gly4238Arg)
c.5870-3437G>C (n.5870-3437G>C)
2g.21002710C>TCA345970642APOBc.12712G>A (p.Gly4238Ser)
c.5870-3437G>A (n.5870-3437G>A)
2g.21002711A>CCA345970644APOBc.12711T>G (p.Asn4237Lys)
c.5870-3438T>G (n.5870-3438T>G)
2g.21002711A>GCA425342408APOBc.12711T>C (p.Asn4237=)
c.5870-3438T>C (n.5870-3438T>C)
gnomAD v4
2g.21002711A>TCA345970645APOBc.12711T>A (p.Asn4237Lys)
c.5870-3438T>A (n.5870-3438T>A)
2g.21002712T>ACA345970646APOBc.12710A>T (p.Asn4237Ile)
c.5870-3439A>T (n.5870-3439A>T)
2g.21002712T>CCA345970648APOBc.12710A>G (p.Asn4237Ser)
c.5870-3439A>G (n.5870-3439A>G)
2g.21002712T>GCA345970647APOBc.12710A>C (p.Asn4237Thr)
c.5870-3439A>C (n.5870-3439A>C)
2g.21002713T>ACA345970649APOBc.12709A>T (p.Asn4237Tyr)
c.5870-3440A>T (n.5870-3440A>T)
2g.21002713T>CCA345970650APOBc.12709A>G (p.Asn4237Asp)
c.5870-3440A>G (n.5870-3440A>G)
2g.21002713T>GCA345970651APOBc.12709A>C (p.Asn4237His)
c.5870-3440A>C (n.5870-3440A>C)
2g.21002714A>CCA345970652APOBc.12708T>G (p.His4236Gln)
c.5870-3441T>G (n.5870-3441T>G)
2g.21002714A>GCA425342412APOBc.12708T>C (p.His4236=)
c.5870-3441T>C (n.5870-3441T>C)
2g.21002714A>TCA345970653APOBc.12708T>A (p.His4236Gln)
c.5870-3441T>A (n.5870-3441T>A)
2g.21002715T>ACA345970656APOBc.12707A>T (p.His4236Leu)
c.5870-3442A>T (n.5870-3442A>T)
2g.21002715T>CCA345970655APOBc.12707A>G (p.His4236Arg)
c.5870-3442A>G (n.5870-3442A>G)
2g.21002715T>GCA345970654APOBc.12707A>C (p.His4236Pro)
c.5870-3442A>C (n.5870-3442A>C)
2g.21002716G>ACA345970657APOBc.12706C>T (p.His4236Tyr)
c.5870-3443C>T (n.5870-3443C>T)
COSMIC
2g.21002716G>CCA345970658APOBc.12706C>G (p.His4236Asp)
c.5870-3443C>G (n.5870-3443C>G)
2g.21002716G>TCA345970659APOBc.12706C>A (p.His4236Asn)
c.5870-3443C>A (n.5870-3443C>A)
2g.21002717G>ACA425342414APOBc.12705C>T (p.Val4235=)
c.5870-3444C>T (n.5870-3444C>T)
2g.21002717G>CCA425342416APOBc.12705C>G (p.Val4235=)
c.5870-3444C>G (n.5870-3444C>G)
2g.21002717G>TCA425342415APOBc.12705C>A (p.Val4235=)
c.5870-3444C>A (n.5870-3444C>A)
2g.21002718A=CA2493473104APOBc.12704T= (p.Val4235=)
c.5870-3445T= (n.5870-3445T=)
2g.21002718A>CCA345970660APOBc.12704T>G (p.Val4235Gly)
c.5870-3445T>G (n.5870-3445T>G)
2g.21002718A>GCA050937APOBc.12704T>C (p.Val4235Ala)
c.5870-3445T>C (n.5870-3445T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21002718A>TCA345970661APOBc.12704T>A (p.Val4235Asp)
c.5870-3445T>A (n.5870-3445T>A)

Number of alleles fetched