Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21009283G>ACA345996835APOBc.7585C>T (p.Gln2529Ter)
c.5869+1450C>T (n.5869+1450C>T)
2g.21009283G>CCA43502306APOBc.7585C>G (p.Gln2529Glu)
c.5869+1450C>G (n.5869+1450C>G)
dbSNP
2g.21009283G=CA2493476170APOBc.7585C= (p.Gln2529=)
c.5869+1450C= (n.5869+1450C=)
2g.21009283G>TCA064549APOBc.7585C>A (p.Gln2529Lys)
c.5869+1450C>A (n.5869+1450C>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009284A=CA2493476171APOBc.7584T= (p.Ile2528=)
c.5869+1449T= (n.5869+1449T=)
2g.21009284A>CCA064544APOBc.7584T>G (p.Ile2528Met)
c.5869+1449T>G (n.5869+1449T>G)
dbSNP ExAC gnomAD v2
2g.21009284A>GCA425344948APOBc.7584T>C (p.Ile2528=)
c.5869+1449T>C (n.5869+1449T>C)
2g.21009284A>TCA425344949APOBc.7584T>A (p.Ile2528=)
c.5869+1449T>A (n.5869+1449T>A)
2g.21009285A>CCA345996837APOBc.7583T>G (p.Ile2528Ser)
c.5869+1448T>G (n.5869+1448T>G)
2g.21009285A>GCA345996838APOBc.7583T>C (p.Ile2528Thr)
c.5869+1448T>C (n.5869+1448T>C)
2g.21009285A>TCA345996836APOBc.7583T>A (p.Ile2528Asn)
c.5869+1448T>A (n.5869+1448T>A)
2g.21009286T>ACA345996839APOBc.7582A>T (p.Ile2528Phe)
c.5869+1447A>T (n.5869+1447A>T)
2g.21009286T>CCA064540APOBc.7582A>G (p.Ile2528Val)
c.5869+1447A>G (n.5869+1447A>G)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.21009286T>GCA345996840APOBc.7582A>C (p.Ile2528Leu)
c.5869+1447A>C (n.5869+1447A>C)
2g.21009286T=CA2493476172APOBc.7582A= (p.Ile2528=)
c.5869+1447A= (n.5869+1447A=)
2g.21009287G>ACA425344950APOBc.7581C>T (p.Asp2527=)
c.5869+1446C>T (n.5869+1446C>T)
dbSNP gnomAD v4
2g.21009287G>CCA345996841APOBc.7581C>G (p.Asp2527Glu)
c.5869+1446C>G (n.5869+1446C>G)
2g.21009287G=CA2493476173APOBc.7581C= (p.Asp2527=)
c.5869+1446C= (n.5869+1446C=)
2g.21009287G>TCA345996842APOBc.7581C>A (p.Asp2527Glu)
c.5869+1446C>A (n.5869+1446C>A)
2g.21009288T>ACA345996843APOBc.7580A>T (p.Asp2527Val)
c.5869+1445A>T (n.5869+1445A>T)
2g.21009288T>CCA345996844APOBc.7580A>G (p.Asp2527Gly)
c.5869+1445A>G (n.5869+1445A>G)
dbSNP gnomAD v4
2g.21009288T>GCA345996845APOBc.7580A>C (p.Asp2527Ala)
c.5869+1445A>C (n.5869+1445A>C)
2g.21009288T=CA2493476174APOBc.7580A= (p.Asp2527=)
c.5869+1445A= (n.5869+1445A=)
2g.21009289C>ACA345996846APOBc.7579G>T (p.Asp2527Tyr)
c.5869+1444G>T (n.5869+1444G>T)
2g.21009289C>GCA345996847APOBc.7579G>C (p.Asp2527His)
c.5869+1444G>C (n.5869+1444G>C)
2g.21009289C>TCA345996848APOBc.7579G>A (p.Asp2527Asn)
c.5869+1444G>A (n.5869+1444G>A)
COSMIC
2g.21009290C>ACA345996851APOBc.7578G>T (p.Met2526Ile)
c.5869+1443G>T (n.5869+1443G>T)
2g.21009290C>GCA345996850APOBc.7578G>C (p.Met2526Ile)
c.5869+1443G>C (n.5869+1443G>C)
2g.21009290C>TCA345996849APOBc.7578G>A (p.Met2526Ile)
c.5869+1443G>A (n.5869+1443G>A)
2g.21009291A=CA2493476175APOBc.7577T= (p.Met2526=)
c.5869+1442T= (n.5869+1442T=)
2g.21009291A>CCA345996852APOBc.7577T>G (p.Met2526Arg)
c.5869+1442T>G (n.5869+1442T>G)
ClinVar gnomAD v4
2g.21009291A>GCA064535APOBc.7577T>C (p.Met2526Thr)
c.5869+1442T>C (n.5869+1442T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009291A>TCA345996853APOBc.7577T>A (p.Met2526Lys)
c.5869+1442T>A (n.5869+1442T>A)
gnomAD v4
2g.21009292T>ACA345996854APOBc.7576A>T (p.Met2526Leu)
c.5869+1441A>T (n.5869+1441A>T)
2g.21009292T>CCA345996855APOBc.7576A>G (p.Met2526Val)
c.5869+1441A>G (n.5869+1441A>G)
dbSNP
2g.21009292T>GCA345996856APOBc.7576A>C (p.Met2526Leu)
c.5869+1441A>C (n.5869+1441A>C)
2g.21009292T=CA2493476176APOBc.7576A= (p.Met2526=)
c.5869+1441A= (n.5869+1441A=)
2g.21009293T>ACA345996857APOBc.7575A>T (p.Gln2525His)
c.5869+1440A>T (n.5869+1440A>T)
2g.21009293T>CCA064527APOBc.7575A>G (p.Gln2525=)
c.5869+1440A>G (n.5869+1440A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009293T>GCA345996858APOBc.7575A>C (p.Gln2525His)
c.5869+1440A>C (n.5869+1440A>C)
2g.21009293T=CA2493476177APOBc.7575A= (p.Gln2525=)
c.5869+1440A= (n.5869+1440A=)
2g.21009294T>ACA345996859APOBc.7574A>T (p.Gln2525Leu)
c.5869+1439A>T (n.5869+1439A>T)
2g.21009294T>CCA345996860APOBc.7574A>G (p.Gln2525Arg)
c.5869+1439A>G (n.5869+1439A>G)
2g.21009294T>GCA345996861APOBc.7574A>C (p.Gln2525Pro)
c.5869+1439A>C (n.5869+1439A>C)
2g.21009295G>ACA345996864APOBc.7573C>T (p.Gln2525Ter)
c.5869+1438C>T (n.5869+1438C>T)
2g.21009295G>CCA345996862APOBc.7573C>G (p.Gln2525Glu)
c.5869+1438C>G (n.5869+1438C>G)
COSMIC
2g.21009295G>TCA345996863APOBc.7573C>A (p.Gln2525Lys)
c.5869+1438C>A (n.5869+1438C>A)
2g.21009296A>CCA345996865APOBc.7572T>G (p.Tyr2524Ter)
c.5869+1437T>G (n.5869+1437T>G)
2g.21009296A>GCA425344955APOBc.7572T>C (p.Tyr2524=)
c.5869+1437T>C (n.5869+1437T>C)
2g.21009296A>TCA345996866APOBc.7572T>A (p.Tyr2524Ter)
c.5869+1437T>A (n.5869+1437T>A)
2g.21009297T>ACA345996867APOBc.7571A>T (p.Tyr2524Phe)
c.5869+1436A>T (n.5869+1436A>T)
2g.21009297T>CCA345996869APOBc.7571A>G (p.Tyr2524Cys)
c.5869+1436A>G (n.5869+1436A>G)
2g.21009297T>GCA345996868APOBc.7571A>C (p.Tyr2524Ser)
c.5869+1436A>C (n.5869+1436A>C)
2g.21009298A=CA2493476178APOBc.7570T= (p.Tyr2524=)
c.5869+1435T= (n.5869+1435T=)
2g.21009298A>CCA345996870APOBc.7570T>G (p.Tyr2524Asp)
c.5869+1435T>G (n.5869+1435T>G)
2g.21009298A>GCA43502361APOBc.7570T>C (p.Tyr2524His)
c.5869+1435T>C (n.5869+1435T>C)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21009298A>TCA345996871APOBc.7570T>A (p.Tyr2524Asn)
c.5869+1435T>A (n.5869+1435T>A)
2g.21009299C>ACA345996872APOBc.7569G>T (p.Met2523Ile)
c.5869+1434G>T (n.5869+1434G>T)
2g.21009299C=CA2493476179APOBc.7569G= (p.Met2523=)
c.5869+1434G= (n.5869+1434G=)
2g.21009299C>GCA345996873APOBc.7569G>C (p.Met2523Ile)
c.5869+1434G>C (n.5869+1434G>C)
2g.21009299C>TCA43502390APOBc.7569G>A (p.Met2523Ile)
c.5869+1434G>A (n.5869+1434G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21009300A=CA2493476180APOBc.7568T= (p.Met2523=)
c.5869+1433T= (n.5869+1433T=)
2g.21009300A>CCA43502412APOBc.7568T>G (p.Met2523Arg)
c.5869+1433T>G (n.5869+1433T>G)
dbSNP
2g.21009300A>GCA345996874APOBc.7568T>C (p.Met2523Thr)
c.5869+1433T>C (n.5869+1433T>C)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009300A>TCA345996875APOBc.7568T>A (p.Met2523Lys)
c.5869+1433T>A (n.5869+1433T>A)
2g.21009301T>ACA345996876APOBc.7567A>T (p.Met2523Leu)
c.5869+1432A>T (n.5869+1432A>T)
2g.21009301T>CCA345996877APOBc.7567A>G (p.Met2523Val)
c.5869+1432A>G (n.5869+1432A>G)
ClinVar
2g.21009301T>GCA345996878APOBc.7567A>C (p.Met2523Leu)
c.5869+1432A>C (n.5869+1432A>C)
ClinVar
2g.21009302T>ACA425344958APOBc.7566A>T (p.Arg2522=)
c.5869+1431A>T (n.5869+1431A>T)
2g.21009302T>CCA064523APOBc.7566A>G (p.Arg2522=)
c.5869+1431A>G (n.5869+1431A>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009302T>GCA425344959APOBc.7566A>C (p.Arg2522=)
c.5869+1431A>C (n.5869+1431A>C)
2g.21009302T=CA2493476181APOBc.7566A= (p.Arg2522=)
c.5869+1431A= (n.5869+1431A=)
2g.21009303C>ACA345996879APOBc.7565G>T (p.Arg2522Leu)
c.5869+1430G>T (n.5869+1430G>T)
gnomAD v4
2g.21009303C=CA2493476182APOBc.7565G= (p.Arg2522=)
c.5869+1430G= (n.5869+1430G=)
2g.21009303C>GCA345996880APOBc.7565G>C (p.Arg2522Pro)
c.5869+1430G>C (n.5869+1430G>C)
2g.21009303C>TCA064517APOBc.7565G>A (p.Arg2522Gln)
c.5869+1430G>A (n.5869+1430G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21009304G>ACA022919APOBc.7564C>T (p.Arg2522Ter)
c.5869+1429C>T (n.5869+1429C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21009304G>CCA345996881APOBc.7564C>G (p.Arg2522Gly)
c.5869+1429C>G (n.5869+1429C>G)
2g.21009304G=CA2493476183APOBc.7564C= (p.Arg2522=)
c.5869+1429C= (n.5869+1429C=)
2g.21009304G>TCA425344960APOBc.7564C>A (p.Arg2522=)
c.5869+1429C>A (n.5869+1429C>A)
2g.21009305G>ACA425344961APOBc.7563C>T (p.Asp2521=)
c.5869+1428C>T (n.5869+1428C>T)
2g.21009305G>CCA345996882APOBc.7563C>G (p.Asp2521Glu)
c.5869+1428C>G (n.5869+1428C>G)
2g.21009305G>TCA345996883APOBc.7563C>A (p.Asp2521Glu)
c.5869+1428C>A (n.5869+1428C>A)
2g.21009306T>ACA345996884APOBc.7562A>T (p.Asp2521Val)
c.5869+1427A>T (n.5869+1427A>T)
2g.21009306T>CCA345996885APOBc.7562A>G (p.Asp2521Gly)
c.5869+1427A>G (n.5869+1427A>G)
COSMIC
2g.21009306T>GCA345996886APOBc.7562A>C (p.Asp2521Ala)
c.5869+1427A>C (n.5869+1427A>C)
2g.21009307C>ACA345996887APOBc.7561G>T (p.Asp2521Tyr)
c.5869+1426G>T (n.5869+1426G>T)
2g.21009307C>GCA345996888APOBc.7561G>C (p.Asp2521His)
c.5869+1426G>C (n.5869+1426G>C)
2g.21009307C>TCA345996889APOBc.7561G>A (p.Asp2521Asn)
c.5869+1426G>A (n.5869+1426G>A)
2g.21009308T>ACA425344962APOBc.7560A>T (p.Arg2520=)
c.5869+1425A>T (n.5869+1425A>T)
2g.21009308T>CCA425344963APOBc.7560A>G (p.Arg2520=)
c.5869+1425A>G (n.5869+1425A>G)
2g.21009308T>GCA425344964APOBc.7560A>C (p.Arg2520=)
c.5869+1425A>C (n.5869+1425A>C)
2g.21009309C>ACA345996890APOBc.7559G>T (p.Arg2520Leu)
c.5869+1424G>T (n.5869+1424G>T)
2g.21009309C=CA2493476184APOBc.7559G= (p.Arg2520=)
c.5869+1424G= (n.5869+1424G=)
2g.21009309C>GCA345996891APOBc.7559G>C (p.Arg2520Pro)
c.5869+1424G>C (n.5869+1424G>C)
gnomAD v4
2g.21009309C>TCA43502444APOBc.7559G>A (p.Arg2520Gln)
c.5869+1424G>A (n.5869+1424G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009310G>ACA064509APOBc.7558C>T (p.Arg2520Ter)
c.5869+1423C>T (n.5869+1423C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
2g.21009310G>CCA345996892APOBc.7558C>G (p.Arg2520Gly)
c.5869+1423C>G (n.5869+1423C>G)
dbSNP gnomAD v2 gnomAD v4
2g.21009310G=CA2493476185APOBc.7558C= (p.Arg2520=)
c.5869+1423C= (n.5869+1423C=)
2g.21009310G>TCA425344965APOBc.7558C>A (p.Arg2520=)
c.5869+1423C>A (n.5869+1423C>A)
ClinVar dbSNP gnomAD v4
2g.21009311T>ACA425344966APOBc.7557A>T (p.Thr2519=)
c.5869+1422A>T (n.5869+1422A>T)
2g.21009311T>CCA425344967APOBc.7557A>G (p.Thr2519=)
c.5869+1422A>G (n.5869+1422A>G)
ClinVar dbSNP gnomAD v4
2g.21009311T>GCA425344968APOBc.7557A>C (p.Thr2519=)
c.5869+1422A>C (n.5869+1422A>C)
2g.21009311T=CA2493476186APOBc.7557A= (p.Thr2519=)
c.5869+1422A= (n.5869+1422A=)
2g.21009312G>ACA345996893APOBc.7556C>T (p.Thr2519Ile)
c.5869+1421C>T (n.5869+1421C>T)
2g.21009312G>CCA345996894APOBc.7556C>G (p.Thr2519Arg)
c.5869+1421C>G (n.5869+1421C>G)
2g.21009312G>TCA345996895APOBc.7556C>A (p.Thr2519Lys)
c.5869+1421C>A (n.5869+1421C>A)
2g.21009313T>ACA345996898APOBc.7555A>T (p.Thr2519Ser)
c.5869+1420A>T (n.5869+1420A>T)
2g.21009313T>CCA345996897APOBc.7555A>G (p.Thr2519Ala)
c.5869+1420A>G (n.5869+1420A>G)
gnomAD v4
2g.21009313T>GCA345996896APOBc.7555A>C (p.Thr2519Pro)
c.5869+1420A>C (n.5869+1420A>C)
2g.21009314A=CA2493476187APOBc.7554T= (p.Asp2518=)
c.5869+1419T= (n.5869+1419T=)
2g.21009314A>CCA345996899APOBc.7554T>G (p.Asp2518Glu)
c.5869+1419T>G (n.5869+1419T>G)
2g.21009314A>GCA064504APOBc.7554T>C (p.Asp2518=)
c.5869+1419T>C (n.5869+1419T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009314A>TCA345996900APOBc.7554T>A (p.Asp2518Glu)
c.5869+1419T>A (n.5869+1419T>A)
2g.21009315T>ACA345996901APOBc.7553A>T (p.Asp2518Val)
c.5869+1418A>T (n.5869+1418A>T)
2g.21009315T>CCA345996902APOBc.7553A>G (p.Asp2518Gly)
c.5869+1418A>G (n.5869+1418A>G)
gnomAD v4
2g.21009315T>GCA345996903APOBc.7553A>C (p.Asp2518Ala)
c.5869+1418A>C (n.5869+1418A>C)
2g.21009316C>ACA345996904APOBc.7552G>T (p.Asp2518Tyr)
c.5869+1417G>T (n.5869+1417G>T)
2g.21009316C>GCA345996906APOBc.7552G>C (p.Asp2518His)
c.5869+1417G>C (n.5869+1417G>C)
2g.21009316C>TCA345996905APOBc.7552G>A (p.Asp2518Asn)
c.5869+1417G>A (n.5869+1417G>A)
2g.21009317T>ACA345996907APOBc.7551A>T (p.Glu2517Asp)
c.5869+1416A>T (n.5869+1416A>T)
2g.21009317T>CCA425344969APOBc.7551A>G (p.Glu2517=)
c.5869+1416A>G (n.5869+1416A>G)
2g.21009317T>GCA345996908APOBc.7551A>C (p.Glu2517Asp)
c.5869+1416A>C (n.5869+1416A>C)
2g.21009318T>ACA345996909APOBc.7550A>T (p.Glu2517Val)
c.5869+1415A>T (n.5869+1415A>T)
2g.21009318T>CCA064499APOBc.7550A>G (p.Glu2517Gly)
c.5869+1415A>G (n.5869+1415A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009318T>GCA345996910APOBc.7550A>C (p.Glu2517Ala)
c.5869+1415A>C (n.5869+1415A>C)
2g.21009318T=CA2493476188APOBc.7550A= (p.Glu2517=)
c.5869+1415A= (n.5869+1415A=)
2g.21009319C>ACA345996911APOBc.7549G>T (p.Glu2517Ter)
c.5869+1414G>T (n.5869+1414G>T)
2g.21009319C=CA2493476189APOBc.7549G= (p.Glu2517=)
c.5869+1414G= (n.5869+1414G=)
2g.21009319C>GCA345996912APOBc.7549G>C (p.Glu2517Gln)
c.5869+1414G>C (n.5869+1414G>C)
2g.21009319C>TCA345996913APOBc.7549G>A (p.Glu2517Lys)
c.5869+1414G>A (n.5869+1414G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21009320T>ACA425344974APOBc.7548A>T (p.Leu2516=)
c.5869+1413A>T (n.5869+1413A>T)
2g.21009320T>CCA425344972APOBc.7548A>G (p.Leu2516=)
c.5869+1413A>G (n.5869+1413A>G)
2g.21009320T>GCA425344971APOBc.7548A>C (p.Leu2516=)
c.5869+1413A>C (n.5869+1413A>C)
2g.21009321A>CCA345996914APOBc.7547T>G (p.Leu2516Arg)
c.5869+1412T>G (n.5869+1412T>G)
2g.21009321A>GCA345996915APOBc.7547T>C (p.Leu2516Pro)
c.5869+1412T>C (n.5869+1412T>C)
2g.21009321A>TCA345996916APOBc.7547T>A (p.Leu2516Gln)
c.5869+1412T>A (n.5869+1412T>A)
2g.21009322G>ACA425344978APOBc.7546C>T (p.Leu2516=)
c.5869+1411C>T (n.5869+1411C>T)
2g.21009322G>CCA345996917APOBc.7546C>G (p.Leu2516Val)
c.5869+1411C>G (n.5869+1411C>G)
2g.21009322G>TCA345996918APOBc.7546C>A (p.Leu2516Ile)
c.5869+1411C>A (n.5869+1411C>A)
2g.21009323G>ACA022913APOBc.7545C>T (p.Thr2515=)
c.5869+1410C>T (n.5869+1410C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009323G>CCA425344980APOBc.7545C>G (p.Thr2515=)
c.5869+1410C>G (n.5869+1410C>G)
2g.21009323G=CA2493476190APOBc.7545C= (p.Thr2515=)
c.5869+1410C= (n.5869+1410C=)
2g.21009323G>TCA425344979APOBc.7545C>A (p.Thr2515=)
c.5869+1410C>A (n.5869+1410C>A)
2g.21009324G>ACA345996920APOBc.7544C>T (p.Thr2515Ile)
c.5869+1409C>T (n.5869+1409C>T)
gnomAD v4
2g.21009324G>CCA345996919APOBc.7544C>G (p.Thr2515Ser)
c.5869+1409C>G (n.5869+1409C>G)
2g.21009324G>TCA345996921APOBc.7544C>A (p.Thr2515Asn)
c.5869+1409C>A (n.5869+1409C>A)
2g.21009325T>ACA345996922APOBc.7543A>T (p.Thr2515Ser)
c.5869+1408A>T (n.5869+1408A>T)
2g.21009325T>CCA345996923APOBc.7543A>G (p.Thr2515Ala)
c.5869+1408A>G (n.5869+1408A>G)
2g.21009325T>GCA345996924APOBc.7543A>C (p.Thr2515Pro)
c.5869+1408A>C (n.5869+1408A>C)
2g.21009326C>ACA345996925APOBc.7542G>T (p.Glu2514Asp)
c.5869+1407G>T (n.5869+1407G>T)
2g.21009326C=CA2493476191APOBc.7542G= (p.Glu2514=)
c.5869+1407G= (n.5869+1407G=)
2g.21009326C>GCA345996926APOBc.7542G>C (p.Glu2514Asp)
c.5869+1407G>C (n.5869+1407G>C)
gnomAD v4
2g.21009326C>TCA425344984APOBc.7542G>A (p.Glu2514=)
c.5869+1407G>A (n.5869+1407G>A)
ClinVar dbSNP
2g.21009326_21009327insAGCACA2543603453APOBc.7541_7542insTGCT (p.Glu2514AspfsTer32)
c.5869+1406_5869+1407insTGCT (n.5869+1406_5869+1407insTGCT)
2g.21009327T>ACA345996927APOBc.7541A>T (p.Glu2514Val)
c.5869+1406A>T (n.5869+1406A>T)
2g.21009327T>CCA345996928APOBc.7541A>G (p.Glu2514Gly)
c.5869+1406A>G (n.5869+1406A>G)
2g.21009327T>GCA345996929APOBc.7541A>C (p.Glu2514Ala)
c.5869+1406A>C (n.5869+1406A>C)
2g.21009328C>ACA345996931APOBc.7540G>T (p.Glu2514Ter)
c.5869+1405G>T (n.5869+1405G>T)
2g.21009328C=CA2493476192APOBc.7540G= (p.Glu2514=)
c.5869+1405G= (n.5869+1405G=)
2g.21009328C>GCA345996933APOBc.7540G>C (p.Glu2514Gln)
c.5869+1405G>C (n.5869+1405G>C)
2g.21009328C>TCA345996934APOBc.7540G>A (p.Glu2514Lys)
c.5869+1405G>A (n.5869+1405G>A)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21009329T>ACA425344991APOBc.7539A>T (p.Arg2513=)
c.5869+1404A>T (n.5869+1404A>T)
2g.21009329T>CCA425344992APOBc.7539A>G (p.Arg2513=)
c.5869+1404A>G (n.5869+1404A>G)
2g.21009329T>GCA425344993APOBc.7539A>C (p.Arg2513=)
c.5869+1404A>C (n.5869+1404A>C)
2g.21009330_21009335delCA2529111314APOBc.7534_7539del (p.Phe2512_Arg2513del)
c.5869+1399_5869+1404del (n.5869+1399_5869+1404del)
2g.21009330C>ACA345996935APOBc.7538G>T (p.Arg2513Leu)
c.5869+1403G>T (n.5869+1403G>T)
2g.21009330C=CA2493476193APOBc.7538G= (p.Arg2513=)
c.5869+1403G= (n.5869+1403G=)
2g.21009330C>GCA345996936APOBc.7538G>C (p.Arg2513Pro)
c.5869+1403G>C (n.5869+1403G>C)
2g.21009330C>TCA064490APOBc.7538G>A (p.Arg2513Gln)
c.5869+1403G>A (n.5869+1403G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21009331G>ACA064481APOBc.7537C>T (p.Arg2513Ter)
c.5869+1402C>T (n.5869+1402C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
2g.21009331G>CCA064473APOBc.7537C>G (p.Arg2513Gly)
c.5869+1402C>G (n.5869+1402C>G)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009331G=CA2493476194APOBc.7537C= (p.Arg2513=)
c.5869+1402C= (n.5869+1402C=)
2g.21009331G>TCA425344999APOBc.7537C>A (p.Arg2513=)
c.5869+1402C>A (n.5869+1402C>A)
2g.21009332G>ACA425345000APOBc.7536C>T (p.Phe2512=)
c.5869+1401C>T (n.5869+1401C>T)
2g.21009332G>CCA345996937APOBc.7536C>G (p.Phe2512Leu)
c.5869+1401C>G (n.5869+1401C>G)
2g.21009332G>TCA345996938APOBc.7536C>A (p.Phe2512Leu)
c.5869+1401C>A (n.5869+1401C>A)
2g.21009333A>CCA345996939APOBc.7535T>G (p.Phe2512Cys)
c.5869+1400T>G (n.5869+1400T>G)
2g.21009333A>GCA345996940APOBc.7535T>C (p.Phe2512Ser)
c.5869+1400T>C (n.5869+1400T>C)
2g.21009333A>TCA345996941APOBc.7535T>A (p.Phe2512Tyr)
c.5869+1400T>A (n.5869+1400T>A)
2g.21009334A>CCA345996942APOBc.7534T>G (p.Phe2512Val)
c.5869+1399T>G (n.5869+1399T>G)
2g.21009334A>GCA345996943APOBc.7534T>C (p.Phe2512Leu)
c.5869+1399T>C (n.5869+1399T>C)
2g.21009334A>TCA345996944APOBc.7534T>A (p.Phe2512Ile)
c.5869+1399T>A (n.5869+1399T>A)
2g.21009335T>ACA345996945APOBc.7533A>T (p.Lys2511Asn)
c.5869+1398A>T (n.5869+1398A>T)
2g.21009335T>CCA425345002APOBc.7533A>G (p.Lys2511=)
c.5869+1398A>G (n.5869+1398A>G)
COSMIC
2g.21009335T>GCA345996946APOBc.7533A>C (p.Lys2511Asn)
c.5869+1398A>C (n.5869+1398A>C)
2g.21009336T>ACA345996947APOBc.7532A>T (p.Lys2511Ile)
c.5869+1397A>T (n.5869+1397A>T)
2g.21009336T>CCA345996948APOBc.7532A>G (p.Lys2511Arg)
c.5869+1397A>G (n.5869+1397A>G)
2g.21009336T>GCA345996949APOBc.7532A>C (p.Lys2511Thr)
c.5869+1397A>C (n.5869+1397A>C)
2g.21009337T>ACA345996950APOBc.7531A>T (p.Lys2511Ter)
c.5869+1396A>T (n.5869+1396A>T)
2g.21009337T>CCA345996952APOBc.7531A>G (p.Lys2511Glu)
c.5869+1396A>G (n.5869+1396A>G)
2g.21009337T>GCA345996951APOBc.7531A>C (p.Lys2511Gln)
c.5869+1396A>C (n.5869+1396A>C)
2g.21009338G>ACA425345006APOBc.7530C>T (p.Ala2510=)
c.5869+1395C>T (n.5869+1395C>T)
2g.21009338G>CCA425345007APOBc.7530C>G (p.Ala2510=)
c.5869+1395C>G (n.5869+1395C>G)
2g.21009338G>TCA425345008APOBc.7530C>A (p.Ala2510=)
c.5869+1395C>A (n.5869+1395C>A)
2g.21009339G>ACA345996953APOBc.7529C>T (p.Ala2510Val)
c.5869+1394C>T (n.5869+1394C>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21009339G>CCA345996954APOBc.7529C>G (p.Ala2510Gly)
c.5869+1394C>G (n.5869+1394C>G)
2g.21009339G=CA2493476195APOBc.7529C= (p.Ala2510=)
c.5869+1394C= (n.5869+1394C=)
2g.21009339G>TCA345996955APOBc.7529C>A (p.Ala2510Asp)
c.5869+1394C>A (n.5869+1394C>A)
2g.21009340C>ACA345996956APOBc.7528G>T (p.Ala2510Ser)
c.5869+1393G>T (n.5869+1393G>T)
2g.21009340C>GCA345996957APOBc.7528G>C (p.Ala2510Pro)
c.5869+1393G>C (n.5869+1393G>C)
2g.21009340C>TCA345996958APOBc.7528G>A (p.Ala2510Thr)
c.5869+1393G>A (n.5869+1393G>A)
gnomAD v4
2g.21009341_21009342insGCAGTGTGGTGCGCGAAATGAACCGCGTCGGCATGATGGTCGACCCA2540602855APOBc.7528_7529insTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCACACTGCGG (p.Lys2509_Ala2510insValAspHisHisAlaAspAlaValHisPheAlaHisHisThrAla)
c.5869+1393_5869+1394insTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCACACTGCGG (n.5869+1393_5869+1394insTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCACACTGCGG)
2g.21009341_21009344dupCA2658056029APOBc.7525_7528dup (p.Ala2510GlufsTer?)
c.5869+1390_5869+1393dup (n.5869+1390_5869+1393dup)
gnomAD v4
2g.21009341C>ACA345996960APOBc.7527G>T (p.Lys2509Asn)
c.5869+1392G>T (n.5869+1392G>T)
2g.21009341C>GCA345996959APOBc.7527G>C (p.Lys2509Asn)
c.5869+1392G>C (n.5869+1392G>C)
2g.21009341C>TCA425345013APOBc.7527G>A (p.Lys2509=)
c.5869+1392G>A (n.5869+1392G>A)
2g.21009341_21009342insGCAGCA2568708330APOBc.7526_7527insCTGC (p.Lys2509AsnfsTer?)
c.5869+1391_5869+1392insCTGC (n.5869+1391_5869+1392insCTGC)
2g.21009342T>ACA345996961APOBc.7526A>T (p.Lys2509Met)
c.5869+1391A>T (n.5869+1391A>T)
2g.21009342T>CCA345996962APOBc.7526A>G (p.Lys2509Arg)
c.5869+1391A>G (n.5869+1391A>G)
2g.21009342T>GCA345996963APOBc.7526A>C (p.Lys2509Thr)
c.5869+1391A>C (n.5869+1391A>C)
2g.21009342_21009343insGTGGTGCGCGAAATGAACCGCGTCGGCATGATGGTCGACCTTTCGCACGGCGCCGAGACGAGTTTCTACGACGTCCTCGAGGTTTCTGCGCTGCCCATTGTGTGCAGCCACCA2556779076APOBc.7525_7526insGTGGCTGCACACAATGGGCAGCGCAGAAACCTCGAGGACGTCGTAGAAACTCGTCTCGGCGCCGTGCGAAAGGTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCAC (p.Lys2509delinsSerGlyCysThrGlnTrpAlaAlaGlnLysProArgGlyArgArgArgAsnSerSerArgArgArgAlaLysGlyArgProSerCysArgArgGlySerPheArgAlaProGln)
c.5869+1390_5869+1391insGTGGCTGCACACAATGGGCAGCGCAGAAACCTCGAGGACGTCGTAGAAACTCGTCTCGGCGCCGTGCGAAAGGTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCAC (n.5869+1390_5869+1391insGTGGCTGCACACAATGGGCAGCGCAGAAACCTCGAGGACGTCGTAGAAACTCGTCTCGGCGCCGTGCGAAAGGTCGACCATCATGCCGACGCGGTTCATTTCGCGCACCAC)
2g.21009343T>ACA345996964APOBc.7525A>T (p.Lys2509Ter)
c.5869+1390A>T (n.5869+1390A>T)
2g.21009343T>CCA345996965APOBc.7525A>G (p.Lys2509Glu)
c.5869+1390A>G (n.5869+1390A>G)
2g.21009343T>GCA345996966APOBc.7525A>C (p.Lys2509Gln)
c.5869+1390A>C (n.5869+1390A>C)
2g.21009343_21009344insTCGCACGGCGCCGAGACGAGTTTCTACGACGCCCTCGAGGTTTCTGCGCTGCA2556349413APOBc.7524_7525insCAGCGCAGAAACCTCGAGGGCGTCGTAGAAACTCGTCTCGGCGCCGTGCGA (p.Met2508_Lys2509insGlnArgArgAsnLeuGluGlyValValGluThrArgLeuGlyAlaValArg)
c.5869+1389_5869+1390insCAGCGCAGAAACCTCGAGGGCGTCGTAGAAACTCGTCTCGGCGCCGTGCGA (n.5869+1389_5869+1390insCAGCGCAGAAACCTCGAGGGCGTCGTAGAAACTCGTCTCGGCGCCGTGCGA)
2g.21009344C>ACA345996967APOBc.7524G>T (p.Met2508Ile)
c.5869+1389G>T (n.5869+1389G>T)
2g.21009344C>GCA345996969APOBc.7524G>C (p.Met2508Ile)
c.5869+1389G>C (n.5869+1389G>C)
2g.21009344C>TCA345996968APOBc.7524G>A (p.Met2508Ile)
c.5869+1389G>A (n.5869+1389G>A)
2g.21009345A=CA2493476196APOBc.7523T= (p.Met2508=)
c.5869+1388T= (n.5869+1388T=)
2g.21009345A>CCA345996970APOBc.7523T>G (p.Met2508Arg)
c.5869+1388T>G (n.5869+1388T>G)
2g.21009345A>GCA345996971APOBc.7523T>C (p.Met2508Thr)
c.5869+1388T>C (n.5869+1388T>C)
dbSNP
2g.21009345A>TCA345996972APOBc.7523T>A (p.Met2508Lys)
c.5869+1388T>A (n.5869+1388T>A)
ClinVar dbSNP gnomAD v3 gnomAD v4
2g.21009346T>ACA345996973APOBc.7522A>T (p.Met2508Leu)
c.5869+1387A>T (n.5869+1387A>T)
2g.21009346T>CCA345996974APOBc.7522A>G (p.Met2508Val)
c.5869+1387A>G (n.5869+1387A>G)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009346T>GCA345996975APOBc.7522A>C (p.Met2508Leu)
c.5869+1387A>C (n.5869+1387A>C)
2g.21009346T=CA2493476197APOBc.7522A= (p.Met2508=)
c.5869+1387A= (n.5869+1387A=)
2g.21009347G>ACA425345021APOBc.7521C>T (p.His2507=)
c.5869+1386C>T (n.5869+1386C>T)
2g.21009347G>CCA345996976APOBc.7521C>G (p.His2507Gln)
c.5869+1386C>G (n.5869+1386C>G)
2g.21009347G>TCA345996977APOBc.7521C>A (p.His2507Gln)
c.5869+1386C>A (n.5869+1386C>A)
2g.21009348T>ACA345996978APOBc.7520A>T (p.His2507Leu)
c.5869+1385A>T (n.5869+1385A>T)
2g.21009348T>CCA064468APOBc.7520A>G (p.His2507Arg)
c.5869+1385A>G (n.5869+1385A>G)
ClinVar dbSNP ExAC
2g.21009348T>GCA064464APOBc.7520A>C (p.His2507Pro)
c.5869+1385A>C (n.5869+1385A>C)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009348T=CA2493476198APOBc.7520A= (p.His2507=)
c.5869+1385A= (n.5869+1385A=)
2g.21009349G>ACA345996979APOBc.7519C>T (p.His2507Tyr)
c.5869+1384C>T (n.5869+1384C>T)
gnomAD v4
2g.21009349G>CCA345996981APOBc.7519C>G (p.His2507Asp)
c.5869+1384C>G (n.5869+1384C>G)
2g.21009349G>TCA345996980APOBc.7519C>A (p.His2507Asn)
c.5869+1384C>A (n.5869+1384C>A)
2g.21009350A>CCA425345023APOBc.7518T>G (p.Ala2506=)
c.5869+1383T>G (n.5869+1383T>G)
2g.21009350A>GCA425345024APOBc.7518T>C (p.Ala2506=)
c.5869+1383T>C (n.5869+1383T>C)
2g.21009350A>TCA425345025APOBc.7518T>A (p.Ala2506=)
c.5869+1383T>A (n.5869+1383T>A)
2g.21009351G>ACA064456APOBc.7517C>T (p.Ala2506Val)
c.5869+1382C>T (n.5869+1382C>T)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21009351G>CCA345996983APOBc.7517C>G (p.Ala2506Gly)
c.5869+1382C>G (n.5869+1382C>G)
2g.21009351G=CA2493476199APOBc.7517C= (p.Ala2506=)
c.5869+1382C= (n.5869+1382C=)
2g.21009351G>TCA345996982APOBc.7517C>A (p.Ala2506Asp)
c.5869+1382C>A (n.5869+1382C>A)
2g.21009352C>ACA345996984APOBc.7516G>T (p.Ala2506Ser)
c.5869+1381G>T (n.5869+1381G>T)
2g.21009352C>GCA345996985APOBc.7516G>C (p.Ala2506Pro)
c.5869+1381G>C (n.5869+1381G>C)
2g.21009352C>TCA345996986APOBc.7516G>A (p.Ala2506Thr)
c.5869+1381G>A (n.5869+1381G>A)
2g.21009353C>ACA345996987APOBc.7515G>T (p.Leu2505Phe)
c.5869+1380G>T (n.5869+1380G>T)
2g.21009353C>GCA345996988APOBc.7515G>C (p.Leu2505Phe)
c.5869+1380G>C (n.5869+1380G>C)
gnomAD v4
2g.21009353C>TCA425345028APOBc.7515G>A (p.Leu2505=)
c.5869+1380G>A (n.5869+1380G>A)
2g.21009354A>CCA345996989APOBc.7514T>G (p.Leu2505Trp)
c.5869+1379T>G (n.5869+1379T>G)
2g.21009354A>GCA345996990APOBc.7514T>C (p.Leu2505Ser)
c.5869+1379T>C (n.5869+1379T>C)
2g.21009354A>TCA345996991APOBc.7514T>A (p.Leu2505Ter)
c.5869+1379T>A (n.5869+1379T>A)
2g.21009355A>CCA345996992APOBc.7513T>G (p.Leu2505Val)
c.5869+1378T>G (n.5869+1378T>G)
2g.21009355A>GCA425345034APOBc.7513T>C (p.Leu2505=)
c.5869+1378T>C (n.5869+1378T>C)
2g.21009355A>TCA345996993APOBc.7513T>A (p.Leu2505Met)
c.5869+1378T>A (n.5869+1378T>A)
2g.21009356A>CCA425345036APOBc.7512T>G (p.Ser2504=)
c.5869+1377T>G (n.5869+1377T>G)
2g.21009356A>GCA425345037APOBc.7512T>C (p.Ser2504=)
c.5869+1377T>C (n.5869+1377T>C)
2g.21009356A>TCA425345038APOBc.7512T>A (p.Ser2504=)
c.5869+1377T>A (n.5869+1377T>A)
2g.21009357G>ACA345996994APOBc.7511C>T (p.Ser2504Phe)
c.5869+1376C>T (n.5869+1376C>T)
ClinVar gnomAD v4
2g.21009357G>CCA345996995APOBc.7511C>G (p.Ser2504Cys)
c.5869+1376C>G (n.5869+1376C>G)
2g.21009357G>TCA345996996APOBc.7511C>A (p.Ser2504Tyr)
c.5869+1376C>A (n.5869+1376C>A)
COSMIC
2g.21009358A=CA2493476200APOBc.7510T= (p.Ser2504=)
c.5869+1375T= (n.5869+1375T=)
2g.21009358A>CCA345996999APOBc.7510T>G (p.Ser2504Ala)
c.5869+1375T>G (n.5869+1375T>G)
2g.21009358A>GCA345996997APOBc.7510T>C (p.Ser2504Pro)
c.5869+1375T>C (n.5869+1375T>C)
2g.21009358A>TCA345996998APOBc.7510T>A (p.Ser2504Thr)
c.5869+1375T>A (n.5869+1375T>A)
ClinVar dbSNP gnomAD v4
2g.21009359T>ACA425345041APOBc.7509A>T (p.Ala2503=)
c.5869+1374A>T (n.5869+1374A>T)
2g.21009359T>CCA425345042APOBc.7509A>G (p.Ala2503=)
c.5869+1374A>G (n.5869+1374A>G)
2g.21009359T>GCA425345043APOBc.7509A>C (p.Ala2503=)
c.5869+1374A>C (n.5869+1374A>C)
dbSNP
2g.21009359T=CA2493476201APOBc.7509A= (p.Ala2503=)
c.5869+1374A= (n.5869+1374A=)
2g.21009360G>ACA345997000APOBc.7508C>T (p.Ala2503Val)
c.5869+1373C>T (n.5869+1373C>T)
2g.21009360G>CCA345997001APOBc.7508C>G (p.Ala2503Gly)
c.5869+1373C>G (n.5869+1373C>G)
2g.21009360G>TCA345997002APOBc.7508C>A (p.Ala2503Glu)
c.5869+1373C>A (n.5869+1373C>A)
2g.21009361C>ACA345997003APOBc.7507G>T (p.Ala2503Ser)
c.5869+1372G>T (n.5869+1372G>T)
2g.21009361C>GCA345997004APOBc.7507G>C (p.Ala2503Pro)
c.5869+1372G>C (n.5869+1372G>C)
2g.21009361C>TCA345997005APOBc.7507G>A (p.Ala2503Thr)
c.5869+1372G>A (n.5869+1372G>A)
2g.21009362T>ACA425345047APOBc.7506A>T (p.Ser2502=)
c.5869+1371A>T (n.5869+1371A>T)
2g.21009362T>CCA425345048APOBc.7506A>G (p.Ser2502=)
c.5869+1371A>G (n.5869+1371A>G)
2g.21009362T>GCA425345049APOBc.7506A>C (p.Ser2502=)
c.5869+1371A>C (n.5869+1371A>C)
2g.21009363G>ACA345997006APOBc.7505C>T (p.Ser2502Leu)
c.5869+1370C>T (n.5869+1370C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009363G>CCA345997007APOBc.7505C>G (p.Ser2502Ter)
c.5869+1370C>G (n.5869+1370C>G)
2g.21009363G=CA2493476202APOBc.7505C= (p.Ser2502=)
c.5869+1370C= (n.5869+1370C=)
2g.21009363G>TCA345997008APOBc.7505C>A (p.Ser2502Ter)
c.5869+1370C>A (n.5869+1370C>A)
2g.21009364A>CCA345997009APOBc.7504T>G (p.Ser2502Ala)
c.5869+1369T>G (n.5869+1369T>G)
2g.21009364A>GCA345997010APOBc.7504T>C (p.Ser2502Pro)
c.5869+1369T>C (n.5869+1369T>C)
2g.21009364A>TCA345997011APOBc.7504T>A (p.Ser2502Thr)
c.5869+1369T>A (n.5869+1369T>A)
2g.21009365A>CCA345997012APOBc.7503T>G (p.Ser2501Arg)
c.5869+1368T>G (n.5869+1368T>G)
2g.21009365A>GCA425345051APOBc.7503T>C (p.Ser2501=)
c.5869+1368T>C (n.5869+1368T>C)
gnomAD v4
2g.21009365A>TCA345997013APOBc.7503T>A (p.Ser2501Arg)
c.5869+1368T>A (n.5869+1368T>A)
2g.21009366C>ACA345997014APOBc.7502G>T (p.Ser2501Ile)
c.5869+1367G>T (n.5869+1367G>T)
2g.21009366C=CA2493476203APOBc.7502G= (p.Ser2501=)
c.5869+1367G= (n.5869+1367G=)
2g.21009366C>GCA345997015APOBc.7502G>C (p.Ser2501Thr)
c.5869+1367G>C (n.5869+1367G>C)
2g.21009366C>TCA43502502APOBc.7502G>A (p.Ser2501Asn)
c.5869+1367G>A (n.5869+1367G>A)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009367T>ACA43502520APOBc.7501A>T (p.Ser2501Cys)
c.5869+1366A>T (n.5869+1366A>T)
ClinVar dbSNP gnomAD v4
2g.21009367T>CCA345997016APOBc.7501A>G (p.Ser2501Gly)
c.5869+1366A>G (n.5869+1366A>G)
dbSNP
2g.21009367T>GCA345997017APOBc.7501A>C (p.Ser2501Arg)
c.5869+1366A>C (n.5869+1366A>C)
2g.21009367T=CA2493476204APOBc.7501A= (p.Ser2501=)
c.5869+1366A= (n.5869+1366A=)
2g.21009368T>ACA345997018APOBc.7500A>T (p.Leu2500Phe)
c.5869+1365A>T (n.5869+1365A>T)
2g.21009368T>CCA425345055APOBc.7500A>G (p.Leu2500=)
c.5869+1365A>G (n.5869+1365A>G)
2g.21009368T>GCA345997019APOBc.7500A>C (p.Leu2500Phe)
c.5869+1365A>C (n.5869+1365A>C)
2g.21009369A>CCA345997020APOBc.7499T>G (p.Leu2500Ter)
c.5869+1364T>G (n.5869+1364T>G)
2g.21009369A>GCA345997021APOBc.7499T>C (p.Leu2500Ser)
c.5869+1364T>C (n.5869+1364T>C)
2g.21009369A>TCA345997022APOBc.7499T>A (p.Leu2500Ter)
c.5869+1364T>A (n.5869+1364T>A)
2g.21009370A=CA2493476205APOBc.7498T= (p.Leu2500=)
c.5869+1363T= (n.5869+1363T=)
2g.21009370A>CCA345997023APOBc.7498T>G (p.Leu2500Val)
c.5869+1363T>G (n.5869+1363T>G)
2g.21009370A>GCA425345058APOBc.7498T>C (p.Leu2500=)
c.5869+1363T>C (n.5869+1363T>C)
dbSNP gnomAD v2 gnomAD v4
2g.21009370A>TCA345997024APOBc.7498T>A (p.Leu2500Ile)
c.5869+1363T>A (n.5869+1363T>A)
2g.21009371A>CCA425345059APOBc.7497T>G (p.Ala2499=)
c.5869+1362T>G (n.5869+1362T>G)
2g.21009371A>GCA425345060APOBc.7497T>C (p.Ala2499=)
c.5869+1362T>C (n.5869+1362T>C)
2g.21009371A>TCA425345061APOBc.7497T>A (p.Ala2499=)
c.5869+1362T>A (n.5869+1362T>A)
2g.21009372G>ACA345997026APOBc.7496C>T (p.Ala2499Val)
c.5869+1361C>T (n.5869+1361C>T)
2g.21009372G>CCA345997027APOBc.7496C>G (p.Ala2499Gly)
c.5869+1361C>G (n.5869+1361C>G)
2g.21009372G>TCA345997025APOBc.7496C>A (p.Ala2499Asp)
c.5869+1361C>A (n.5869+1361C>A)
2g.21009373C>ACA345997028APOBc.7495G>T (p.Ala2499Ser)
c.5869+1360G>T (n.5869+1360G>T)
gnomAD v4
2g.21009373C>GCA345997029APOBc.7495G>C (p.Ala2499Pro)
c.5869+1360G>C (n.5869+1360G>C)
gnomAD v4
2g.21009373C>TCA345997030APOBc.7495G>A (p.Ala2499Thr)
c.5869+1360G>A (n.5869+1360G>A)
2g.21009374C>ACA43502529APOBc.7494G>T (p.Glu2498Asp)
c.5869+1359G>T (n.5869+1359G>T)
dbSNP
2g.21009374C=CA2493476206APOBc.7494G= (p.Glu2498=)
c.5869+1359G= (n.5869+1359G=)
2g.21009374C>GCA345997031APOBc.7494G>C (p.Glu2498Asp)
c.5869+1359G>C (n.5869+1359G>C)
2g.21009374C>TCA425345064APOBc.7494G>A (p.Glu2498=)
c.5869+1359G>A (n.5869+1359G>A)
2g.21009375T>ACA345997034APOBc.7493A>T (p.Glu2498Val)
c.5869+1358A>T (n.5869+1358A>T)
2g.21009375T>CCA345997032APOBc.7493A>G (p.Glu2498Gly)
c.5869+1358A>G (n.5869+1358A>G)
gnomAD v4
2g.21009375T>GCA345997033APOBc.7493A>C (p.Glu2498Ala)
c.5869+1358A>C (n.5869+1358A>C)
ClinVar gnomAD v4
2g.21009376C>ACA345997035APOBc.7492G>T (p.Glu2498Ter)
c.5869+1357G>T (n.5869+1357G>T)
2g.21009376C=CA2493476207APOBc.7492G= (p.Glu2498=)
c.5869+1357G= (n.5869+1357G=)
2g.21009376C>GCA345997036APOBc.7492G>C (p.Glu2498Gln)
c.5869+1357G>C (n.5869+1357G>C)
dbSNP
2g.21009376C>TCA345997037APOBc.7492G>A (p.Glu2498Lys)
c.5869+1357G>A (n.5869+1357G>A)
2g.21009377C>ACA43502545APOBc.7491G>T (p.Gln2497His)
c.5869+1356G>T (n.5869+1356G>T)
dbSNP COSMIC
2g.21009377C=CA2493476208APOBc.7491G= (p.Gln2497=)
c.5869+1356G= (n.5869+1356G=)
2g.21009377C>GCA345997038APOBc.7491G>C (p.Gln2497His)
c.5869+1356G>C (n.5869+1356G>C)
2g.21009377C>TCA425345067APOBc.7491G>A (p.Gln2497=)
c.5869+1356G>A (n.5869+1356G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21009378T>ACA345997039APOBc.7490A>T (p.Gln2497Leu)
c.5869+1355A>T (n.5869+1355A>T)
2g.21009378T>CCA345997041APOBc.7490A>G (p.Gln2497Arg)
c.5869+1355A>G (n.5869+1355A>G)
2g.21009378T>GCA345997040APOBc.7490A>C (p.Gln2497Pro)
c.5869+1355A>C (n.5869+1355A>C)
2g.21009379G>ACA345997042APOBc.7489C>T (p.Gln2497Ter)
c.5869+1354C>T (n.5869+1354C>T)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21009379G>CCA345997044APOBc.7489C>G (p.Gln2497Glu)
c.5869+1354C>G (n.5869+1354C>G)
2g.21009379G=CA2493476209APOBc.7489C= (p.Gln2497=)
c.5869+1354C= (n.5869+1354C=)
2g.21009379G>TCA345997043APOBc.7489C>A (p.Gln2497Lys)
c.5869+1354C>A (n.5869+1354C>A)
2g.21009380T>ACA345997045APOBc.7488A>T (p.Leu2496Phe)
c.5869+1353A>T (n.5869+1353A>T)
2g.21009380T>CCA425345070APOBc.7488A>G (p.Leu2496=)
c.5869+1353A>G (n.5869+1353A>G)
2g.21009380T>GCA345997046APOBc.7488A>C (p.Leu2496Phe)
c.5869+1353A>C (n.5869+1353A>C)
2g.21009381A=CA2493476210APOBc.7487T= (p.Leu2496=)
c.5869+1352T= (n.5869+1352T=)
2g.21009381A>CCA345997047APOBc.7487T>G (p.Leu2496Ter)
c.5869+1352T>G (n.5869+1352T>G)
2g.21009381A>GCA345997048APOBc.7487T>C (p.Leu2496Ser)
c.5869+1352T>C (n.5869+1352T>C)
ClinVar dbSNP
2g.21009381A>TCA345997049APOBc.7487T>A (p.Leu2496Ter)
c.5869+1352T>A (n.5869+1352T>A)
2g.21009382A>CCA345997050APOBc.7486T>G (p.Leu2496Val)
c.5869+1351T>G (n.5869+1351T>G)
2g.21009382A>GCA425345075APOBc.7486T>C (p.Leu2496=)
c.5869+1351T>C (n.5869+1351T>C)
2g.21009382A>TCA345997051APOBc.7486T>A (p.Leu2496Ile)
c.5869+1351T>A (n.5869+1351T>A)
2g.21009383C>ACA345997052APOBc.7485G>T (p.Trp2495Cys)
c.5869+1350G>T (n.5869+1350G>T)
2g.21009383C>GCA345997053APOBc.7485G>C (p.Trp2495Cys)
c.5869+1350G>C (n.5869+1350G>C)
2g.21009383C>TCA345997054APOBc.7485G>A (p.Trp2495Ter)
c.5869+1350G>A (n.5869+1350G>A)

Number of alleles fetched