Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21010256_21010259delinsTTCACA2493476610APOBc.6609_6612delinsTGAA (p.Asp2203=)
c.5869+474_5869+477delinsTGAA (n.5869+474_5869+477delinsTGAA)
2g.21010260_21010262delCA16610674APOBc.6609_6611del (p.Asp2203del)
c.5869+474_5869+476del (n.5869+474_5869+476del)
ClinVar dbSNP
2g.21010258C>ACA346001366APOBc.6610G>T (p.Glu2204Ter)
c.5869+475G>T (n.5869+475G>T)
2g.21010258C=CA2493476612APOBc.6610G= (p.Glu2204=)
c.5869+475G= (n.5869+475G=)
2g.21010258C>GCA346001368APOBc.6610G>C (p.Glu2204Gln)
c.5869+475G>C (n.5869+475G>C)
dbSNP
2g.21010258C>TCA346001367APOBc.6610G>A (p.Glu2204Lys)
c.5869+475G>A (n.5869+475G>A)
gnomAD v4
2g.21010259A=CA2493476613APOBc.6609T= (p.Asp2203=)
c.5869+474T= (n.5869+474T=)
2g.21010259A>CCA346001369APOBc.6609T>G (p.Asp2203Glu)
c.5869+474T>G (n.5869+474T>G)
2g.21010259A>GCA43505063APOBc.6609T>C (p.Asp2203=)
c.5869+474T>C (n.5869+474T>C)
dbSNP gnomAD v4
2g.21010259A>TCA346001370APOBc.6609T>A (p.Asp2203Glu)
c.5869+474T>A (n.5869+474T>A)
2g.21010260T>ACA346001371APOBc.6608A>T (p.Asp2203Val)
c.5869+473A>T (n.5869+473A>T)
2g.21010260T>CCA346001372APOBc.6608A>G (p.Asp2203Gly)
c.5869+473A>G (n.5869+473A>G)
gnomAD v4
2g.21010260T>GCA346001373APOBc.6608A>C (p.Asp2203Ala)
c.5869+473A>C (n.5869+473A>C)
2g.21010261C>ACA346001374APOBc.6607G>T (p.Asp2203Tyr)
c.5869+472G>T (n.5869+472G>T)
dbSNP gnomAD v4
2g.21010261C=CA2493476615APOBc.6607G= (p.Asp2203=)
c.5869+472G= (n.5869+472G=)
2g.21010261C>GCA346001375APOBc.6607G>C (p.Asp2203His)
c.5869+472G>C (n.5869+472G>C)
COSMIC
2g.21010261C>TCA346001376APOBc.6607G>A (p.Asp2203Asn)
c.5869+472G>A (n.5869+472G>A)
2g.21010261_21010264delinsCAATCA2493476614APOBc.6604_6607delinsATTG (p.Ile2202=)
c.5869+469_5869+472delinsATTG (n.5869+469_5869+472delinsATTG)
2g.21010262A>CCA346001377APOBc.6606T>G (p.Ile2202Met)
c.5869+471T>G (n.5869+471T>G)
2g.21010262A>GCA425345723APOBc.6606T>C (p.Ile2202=)
c.5869+471T>C (n.5869+471T>C)
gnomAD v4
2g.21010262A>TCA425345724APOBc.6606T>A (p.Ile2202=)
c.5869+471T>A (n.5869+471T>A)
2g.21010266_21010268delCA531312748APOBc.6604_6606del (p.Ile2202del)
c.5869+469_5869+471del (n.5869+469_5869+471del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
2g.21010263A>CCA346001378APOBc.6605T>G (p.Ile2202Ser)
c.5869+470T>G (n.5869+470T>G)
2g.21010263A>GCA346001379APOBc.6605T>C (p.Ile2202Thr)
c.5869+470T>C (n.5869+470T>C)
gnomAD v4
2g.21010263A>TCA346001380APOBc.6605T>A (p.Ile2202Asn)
c.5869+470T>A (n.5869+470T>A)
gnomAD v4
2g.21010264T>ACA063387APOBc.6604A>T (p.Ile2202Phe)
c.5869+469A>T (n.5869+469A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010264T>CCA346001382APOBc.6604A>G (p.Ile2202Val)
c.5869+469A>G (n.5869+469A>G)
2g.21010264T>GCA346001381APOBc.6604A>C (p.Ile2202Leu)
c.5869+469A>C (n.5869+469A>C)
2g.21010264T=CA2493476616APOBc.6604A= (p.Ile2202=)
c.5869+469A= (n.5869+469A=)
2g.21010265A>CCA346001383APOBc.6603T>G (p.Ile2201Met)
c.5869+468T>G (n.5869+468T>G)
2g.21010265A>GCA425345725APOBc.6603T>C (p.Ile2201=)
c.5869+468T>C (n.5869+468T>C)
2g.21010265A>TCA425345726APOBc.6603T>A (p.Ile2201=)
c.5869+468T>A (n.5869+468T>A)
2g.21010266A>CCA346001384APOBc.6602T>G (p.Ile2201Ser)
c.5869+467T>G (n.5869+467T>G)
2g.21010266A>GCA346001385APOBc.6602T>C (p.Ile2201Thr)
c.5869+467T>C (n.5869+467T>C)
2g.21010266A>TCA346001386APOBc.6602T>A (p.Ile2201Asn)
c.5869+467T>A (n.5869+467T>A)
2g.21010267T>ACA346001387APOBc.6601A>T (p.Ile2201Phe)
c.5869+466A>T (n.5869+466A>T)
2g.21010267T>CCA346001388APOBc.6601A>G (p.Ile2201Val)
c.5869+466A>G (n.5869+466A>G)
2g.21010267T>GCA346001389APOBc.6601A>C (p.Ile2201Leu)
c.5869+466A>C (n.5869+466A>C)
2g.21010268A=CA2493476617APOBc.6600T= (p.Asn2200=)
c.5869+465T= (n.5869+465T=)
2g.21010268A>CCA346001390APOBc.6600T>G (p.Asn2200Lys)
c.5869+465T>G (n.5869+465T>G)
dbSNP
2g.21010268A>GCA425345727APOBc.6600T>C (p.Asn2200=)
c.5869+465T>C (n.5869+465T>C)
2g.21010268A>TCA346001391APOBc.6600T>A (p.Asn2200Lys)
c.5869+465T>A (n.5869+465T>A)
2g.21010269T>ACA346001394APOBc.6599A>T (p.Asn2200Ile)
c.5869+464A>T (n.5869+464A>T)
2g.21010269T>CCA346001393APOBc.6599A>G (p.Asn2200Ser)
c.5869+464A>G (n.5869+464A>G)
dbSNP
2g.21010269T>GCA346001392APOBc.6599A>C (p.Asn2200Thr)
c.5869+464A>C (n.5869+464A>C)
2g.21010269T=CA2493476618APOBc.6599A= (p.Asn2200=)
c.5869+464A= (n.5869+464A=)
2g.21010270T>ACA346001395APOBc.6598A>T (p.Asn2200Tyr)
c.5869+463A>T (n.5869+463A>T)
2g.21010270T>CCA346001396APOBc.6598A>G (p.Asn2200Asp)
c.5869+463A>G (n.5869+463A>G)
dbSNP
2g.21010270T>GCA346001397APOBc.6598A>C (p.Asn2200His)
c.5869+463A>C (n.5869+463A>C)
dbSNP
2g.21010270T=CA2493476619APOBc.6598A= (p.Asn2200=)
c.5869+463A= (n.5869+463A=)
2g.21010271A>CCA425345731APOBc.6597T>G (p.Ala2199=)
c.5869+462T>G (n.5869+462T>G)
2g.21010271A>GCA425345730APOBc.6597T>C (p.Ala2199=)
c.5869+462T>C (n.5869+462T>C)
2g.21010271A>TCA425345729APOBc.6597T>A (p.Ala2199=)
c.5869+462T>A (n.5869+462T>A)
2g.21010272G>ACA43505067APOBc.6596C>T (p.Ala2199Val)
c.5869+461C>T (n.5869+461C>T)
ClinVar dbSNP gnomAD v4
2g.21010272G>CCA346001398APOBc.6596C>G (p.Ala2199Gly)
c.5869+461C>G (n.5869+461C>G)
2g.21010272G=CA2493476620APOBc.6596C= (p.Ala2199=)
c.5869+461C= (n.5869+461C=)
2g.21010272G>TCA346001399APOBc.6596C>A (p.Ala2199Asp)
c.5869+461C>A (n.5869+461C>A)
2g.21010273C>ACA346001400APOBc.6595G>T (p.Ala2199Ser)
c.5869+460G>T (n.5869+460G>T)
gnomAD v4
2g.21010273C=CA2493476621APOBc.6595G= (p.Ala2199=)
c.5869+460G= (n.5869+460G=)
2g.21010273C>GCA346001401APOBc.6595G>C (p.Ala2199Pro)
c.5869+460G>C (n.5869+460G>C)
2g.21010273C>TCA063379APOBc.6595G>A (p.Ala2199Thr)
c.5869+460G>A (n.5869+460G>A)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010274A>CCA346001402APOBc.6594T>G (p.Ile2198Met)
c.5869+459T>G (n.5869+459T>G)
2g.21010274A>GCA425345735APOBc.6594T>C (p.Ile2198=)
c.5869+459T>C (n.5869+459T>C)
gnomAD v4
2g.21010274A>TCA425345734APOBc.6594T>A (p.Ile2198=)
c.5869+459T>A (n.5869+459T>A)
2g.21010275A>CCA346001403APOBc.6593T>G (p.Ile2198Ser)
c.5869+458T>G (n.5869+458T>G)
2g.21010275A>GCA346001404APOBc.6593T>C (p.Ile2198Thr)
c.5869+458T>C (n.5869+458T>C)
2g.21010275A>TCA346001405APOBc.6593T>A (p.Ile2198Asn)
c.5869+458T>A (n.5869+458T>A)
2g.21010276T>ACA346001406APOBc.6592A>T (p.Ile2198Phe)
c.5869+457A>T (n.5869+457A>T)
2g.21010276T>CCA346001408APOBc.6592A>G (p.Ile2198Val)
c.5869+457A>G (n.5869+457A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21010276T>GCA346001407APOBc.6592A>C (p.Ile2198Leu)
c.5869+457A>C (n.5869+457A>C)
2g.21010276T=CA2493476622APOBc.6592A= (p.Ile2198=)
c.5869+457A= (n.5869+457A=)
2g.21010277A>CCA425345737APOBc.6591T>G (p.Ala2197=)
c.5869+456T>G (n.5869+456T>G)
2g.21010277A>GCA425345739APOBc.6591T>C (p.Ala2197=)
c.5869+456T>C (n.5869+456T>C)
2g.21010277A>TCA425345741APOBc.6591T>A (p.Ala2197=)
c.5869+456T>A (n.5869+456T>A)
2g.21010278G>ACA346001409APOBc.6590C>T (p.Ala2197Val)
c.5869+455C>T (n.5869+455C>T)
dbSNP
2g.21010278G>CCA346001410APOBc.6590C>G (p.Ala2197Gly)
c.5869+455C>G (n.5869+455C>G)
2g.21010278G=CA2493476623APOBc.6590C= (p.Ala2197=)
c.5869+455C= (n.5869+455C=)
2g.21010278G>TCA346001411APOBc.6590C>A (p.Ala2197Asp)
c.5869+455C>A (n.5869+455C>A)
dbSNP gnomAD v4
2g.21010279C>ACA346001412APOBc.6589G>T (p.Ala2197Ser)
c.5869+454G>T (n.5869+454G>T)
2g.21010279C=CA2493476624APOBc.6589G= (p.Ala2197=)
c.5869+454G= (n.5869+454G=)
2g.21010279C>GCA346001413APOBc.6589G>C (p.Ala2197Pro)
c.5869+454G>C (n.5869+454G>C)
2g.21010279C>TCA346001414APOBc.6589G>A (p.Ala2197Thr)
c.5869+454G>A (n.5869+454G>A)
dbSNP
2g.21010280T>ACA425345744APOBc.6588A>T (p.Ile2196=)
c.5869+453A>T (n.5869+453A>T)
2g.21010280T>CCA346001415APOBc.6588A>G (p.Ile2196Met)
c.5869+453A>G (n.5869+453A>G)
2g.21010280T>GCA425345745APOBc.6588A>C (p.Ile2196=)
c.5869+453A>C (n.5869+453A>C)
2g.21010281A=CA2493476625APOBc.6587T= (p.Ile2196=)
c.5869+452T= (n.5869+452T=)
2g.21010281A>CCA346001416APOBc.6587T>G (p.Ile2196Arg)
c.5869+452T>G (n.5869+452T>G)
dbSNP
2g.21010281A>GCA346001417APOBc.6587T>C (p.Ile2196Thr)
c.5869+452T>C (n.5869+452T>C)
gnomAD v4
2g.21010281A>TCA346001418APOBc.6587T>A (p.Ile2196Lys)
c.5869+452T>A (n.5869+452T>A)
2g.21010282T>ACA346001421APOBc.6586A>T (p.Ile2196Leu)
c.5869+451A>T (n.5869+451A>T)
2g.21010282T>CCA346001420APOBc.6586A>G (p.Ile2196Val)
c.5869+451A>G (n.5869+451A>G)
2g.21010282T>GCA346001419APOBc.6586A>C (p.Ile2196Leu)
c.5869+451A>C (n.5869+451A>C)
2g.21010283T>ACA063372APOBc.6585A>T (p.Lys2195Asn)
c.5869+450A>T (n.5869+450A>T)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010283T>CCA425345746APOBc.6585A>G (p.Lys2195=)
c.5869+450A>G (n.5869+450A>G)
COSMIC
2g.21010283T>GCA346001422APOBc.6585A>C (p.Lys2195Asn)
c.5869+450A>C (n.5869+450A>C)
2g.21010283T=CA2493476626APOBc.6585A= (p.Lys2195=)
c.5869+450A= (n.5869+450A=)
2g.21010284T>ACA346001423APOBc.6584A>T (p.Lys2195Ile)
c.5869+449A>T (n.5869+449A>T)
gnomAD v4
2g.21010284T>CCA346001425APOBc.6584A>G (p.Lys2195Arg)
c.5869+449A>G (n.5869+449A>G)
2g.21010284T>GCA346001424APOBc.6584A>C (p.Lys2195Thr)
c.5869+449A>C (n.5869+449A>C)
2g.21010285T>ACA346001426APOBc.6583A>T (p.Lys2195Ter)
c.5869+448A>T (n.5869+448A>T)
2g.21010285T>CCA346001427APOBc.6583A>G (p.Lys2195Glu)
c.5869+448A>G (n.5869+448A>G)
ClinVar gnomAD v4
2g.21010285T>GCA346001428APOBc.6583A>C (p.Lys2195Gln)
c.5869+448A>C (n.5869+448A>C)
2g.21010286C>ACA346001429APOBc.6582G>T (p.Leu2194Phe)
c.5869+447G>T (n.5869+447G>T)
2g.21010286C=CA2493476627APOBc.6582G= (p.Leu2194=)
c.5869+447G= (n.5869+447G=)
2g.21010286C>GCA346001430APOBc.6582G>C (p.Leu2194Phe)
c.5869+447G>C (n.5869+447G>C)
2g.21010286C>TCA425345748APOBc.6582G>A (p.Leu2194=)
c.5869+447G>A (n.5869+447G>A)
dbSNP
2g.21010287A>CCA346001431APOBc.6581T>G (p.Leu2194Trp)
c.5869+446T>G (n.5869+446T>G)
2g.21010287A>GCA346001432APOBc.6581T>C (p.Leu2194Ser)
c.5869+446T>C (n.5869+446T>C)
2g.21010287A>TCA346001433APOBc.6581T>A (p.Leu2194Ter)
c.5869+446T>A (n.5869+446T>A)
2g.21010294_21010302delCA2658056048APOBc.6573_6581del (p.His2192_Leu2194del)
c.5869+438_5869+446del (n.5869+438_5869+446del)
gnomAD v4
2g.21010288A>CCA346001434APOBc.6580T>G (p.Leu2194Val)
c.5869+445T>G (n.5869+445T>G)
2g.21010288A>GCA425345750APOBc.6580T>C (p.Leu2194=)
c.5869+445T>C (n.5869+445T>C)
2g.21010288A>TCA346001435APOBc.6580T>A (p.Leu2194Met)
c.5869+445T>A (n.5869+445T>A)
2g.21010289A=CA2493476628APOBc.6579T= (p.Asp2193=)
c.5869+444T= (n.5869+444T=)
2g.21010289A>CCA346001436APOBc.6579T>G (p.Asp2193Glu)
c.5869+444T>G (n.5869+444T>G)
gnomAD v4
2g.21010289A>GCA425345753APOBc.6579T>C (p.Asp2193=)
c.5869+444T>C (n.5869+444T>C)
dbSNP
2g.21010289A>TCA346001437APOBc.6579T>A (p.Asp2193Glu)
c.5869+444T>A (n.5869+444T>A)
dbSNP
2g.21010290T>ACA346001440APOBc.6578A>T (p.Asp2193Val)
c.5869+443A>T (n.5869+443A>T)
2g.21010290T>CCA346001438APOBc.6578A>G (p.Asp2193Gly)
c.5869+443A>G (n.5869+443A>G)
2g.21010290T>GCA346001439APOBc.6578A>C (p.Asp2193Ala)
c.5869+443A>C (n.5869+443A>C)
2g.21010291C>ACA346001441APOBc.6577G>T (p.Asp2193Tyr)
c.5869+442G>T (n.5869+442G>T)
gnomAD v4
2g.21010291C=CA2493476629APOBc.6577G= (p.Asp2193=)
c.5869+442G= (n.5869+442G=)
2g.21010291C>GCA346001442APOBc.6577G>C (p.Asp2193His)
c.5869+442G>C (n.5869+442G>C)
2g.21010291C>TCA346001443APOBc.6577G>A (p.Asp2193Asn)
c.5869+442G>A (n.5869+442G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21010292A>CCA346001444APOBc.6576T>G (p.His2192Gln)
c.5869+441T>G (n.5869+441T>G)
2g.21010292A>GCA425345756APOBc.6576T>C (p.His2192=)
c.5869+441T>C (n.5869+441T>C)
gnomAD v4
2g.21010292A>TCA346001445APOBc.6576T>A (p.His2192Gln)
c.5869+441T>A (n.5869+441T>A)
2g.21010293T>ACA346001446APOBc.6575A>T (p.His2192Leu)
c.5869+440A>T (n.5869+440A>T)
2g.21010293T>CCA346001447APOBc.6575A>G (p.His2192Arg)
c.5869+440A>G (n.5869+440A>G)
ClinVar dbSNP gnomAD v4
2g.21010293T>GCA346001448APOBc.6575A>C (p.His2192Pro)
c.5869+440A>C (n.5869+440A>C)
2g.21010293T=CA2493476630APOBc.6575A= (p.His2192=)
c.5869+440A= (n.5869+440A=)
2g.21010294G>ACA346001449APOBc.6574C>T (p.His2192Tyr)
c.5869+439C>T (n.5869+439C>T)
2g.21010294G>CCA346001450APOBc.6574C>G (p.His2192Asp)
c.5869+439C>G (n.5869+439C>G)
2g.21010294G>TCA346001451APOBc.6574C>A (p.His2192Asn)
c.5869+439C>A (n.5869+439C>A)
gnomAD v4
2g.21010295T>ACA346001452APOBc.6573A>T (p.Leu2191Phe)
c.5869+438A>T (n.5869+438A>T)
2g.21010295T>CCA425345757APOBc.6573A>G (p.Leu2191=)
c.5869+438A>G (n.5869+438A>G)
dbSNP gnomAD v3 gnomAD v4
2g.21010295T>GCA346001453APOBc.6573A>C (p.Leu2191Phe)
c.5869+438A>C (n.5869+438A>C)
2g.21010295T=CA2493476631APOBc.6573A= (p.Leu2191=)
c.5869+438A= (n.5869+438A=)
2g.21010296A=CA2493476632APOBc.6572T= (p.Leu2191=)
c.5869+437T= (n.5869+437T=)
2g.21010296A>CCA346001454APOBc.6572T>G (p.Leu2191Ter)
c.5869+437T>G (n.5869+437T>G)
2g.21010296A>GCA063363APOBc.6572T>C (p.Leu2191Ser)
c.5869+437T>C (n.5869+437T>C)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010296A>TCA346001455APOBc.6572T>A (p.Leu2191Ter)
c.5869+437T>A (n.5869+437T>A)
2g.21010297A=CA2493476633APOBc.6571T= (p.Leu2191=)
c.5869+436T= (n.5869+436T=)
2g.21010297A>CCA346001456APOBc.6571T>G (p.Leu2191Val)
c.5869+436T>G (n.5869+436T>G)
dbSNP gnomAD v2 gnomAD v4
2g.21010297A>GCA425345760APOBc.6571T>C (p.Leu2191=)
c.5869+436T>C (n.5869+436T>C)
ClinVar dbSNP gnomAD v4
2g.21010297A>TCA346001457APOBc.6571T>A (p.Leu2191Ile)
c.5869+436T>A (n.5869+436T>A)
ClinVar gnomAD v4
2g.21010298A>CCA346001458APOBc.6570T>G (p.Asp2190Glu)
c.5869+435T>G (n.5869+435T>G)
2g.21010298A>GCA425345761APOBc.6570T>C (p.Asp2190=)
c.5869+435T>C (n.5869+435T>C)
2g.21010298A>TCA346001459APOBc.6570T>A (p.Asp2190Glu)
c.5869+435T>A (n.5869+435T>A)
2g.21010299T>ACA346001460APOBc.6569A>T (p.Asp2190Val)
c.5869+434A>T (n.5869+434A>T)
2g.21010299T>CCA346001461APOBc.6569A>G (p.Asp2190Gly)
c.5869+434A>G (n.5869+434A>G)
gnomAD v4
2g.21010299T>GCA346001462APOBc.6569A>C (p.Asp2190Ala)
c.5869+434A>C (n.5869+434A>C)
2g.21010300C>ACA346001463APOBc.6568G>T (p.Asp2190Tyr)
c.5869+433G>T (n.5869+433G>T)
dbSNP gnomAD v3 gnomAD v4
2g.21010300C=CA2493476634APOBc.6568G= (p.Asp2190=)
c.5869+433G= (n.5869+433G=)
2g.21010300C>GCA346001464APOBc.6568G>C (p.Asp2190His)
c.5869+433G>C (n.5869+433G>C)
2g.21010300C>TCA346001465APOBc.6568G>A (p.Asp2190Asn)
c.5869+433G>A (n.5869+433G>A)
2g.21010301A=CA2493476635APOBc.6567T= (p.Tyr2189=)
c.5869+432T= (n.5869+432T=)
2g.21010301A>CCA346001466APOBc.6567T>G (p.Tyr2189Ter)
c.5869+432T>G (n.5869+432T>G)
2g.21010301A>GCA425345766APOBc.6567T>C (p.Tyr2189=)
c.5869+432T>C (n.5869+432T>C)
gnomAD v4
2g.21010301A>TCA346001467APOBc.6567T>A (p.Tyr2189Ter)
c.5869+432T>A (n.5869+432T>A)
ClinVar dbSNP
2g.21010302T>ACA346001468APOBc.6566A>T (p.Tyr2189Phe)
c.5869+431A>T (n.5869+431A>T)
2g.21010302T>CCA346001469APOBc.6566A>G (p.Tyr2189Cys)
c.5869+431A>G (n.5869+431A>G)
gnomAD v4 COSMIC
2g.21010302T>GCA346001470APOBc.6566A>C (p.Tyr2189Ser)
c.5869+431A>C (n.5869+431A>C)
2g.21010303A>CCA346001471APOBc.6565T>G (p.Tyr2189Asp)
c.5869+430T>G (n.5869+430T>G)
2g.21010303A>GCA346001472APOBc.6565T>C (p.Tyr2189His)
c.5869+430T>C (n.5869+430T>C)
2g.21010303A>TCA346001473APOBc.6565T>A (p.Tyr2189Asn)
c.5869+430T>A (n.5869+430T>A)
2g.21010304A=CA2493476636APOBc.6564T= (p.Ser2188=)
c.5869+429T= (n.5869+429T=)
2g.21010304A>CCA346001474APOBc.6564T>G (p.Ser2188Arg)
c.5869+429T>G (n.5869+429T>G)
2g.21010304A>GCA063352APOBc.6564T>C (p.Ser2188=)
c.5869+429T>C (n.5869+429T>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010304A>TCA346001475APOBc.6564T>A (p.Ser2188Arg)
c.5869+429T>A (n.5869+429T>A)
2g.21010305C>ACA346001476APOBc.6563G>T (p.Ser2188Ile)
c.5869+428G>T (n.5869+428G>T)
gnomAD v4
2g.21010305C=CA2493476637APOBc.6563G= (p.Ser2188=)
c.5869+428G= (n.5869+428G=)
2g.21010305C>GCA346001477APOBc.6563G>C (p.Ser2188Thr)
c.5869+428G>C (n.5869+428G>C)
2g.21010305C>TCA063344APOBc.6563G>A (p.Ser2188Asn)
c.5869+428G>A (n.5869+428G>A)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010306T>ACA346001479APOBc.6562A>T (p.Ser2188Cys)
c.5869+427A>T (n.5869+427A>T)
2g.21010306T>CCA346001480APOBc.6562A>G (p.Ser2188Gly)
c.5869+427A>G (n.5869+427A>G)
gnomAD v4
2g.21010306T>GCA346001478APOBc.6562A>C (p.Ser2188Arg)
c.5869+427A>C (n.5869+427A>C)
2g.21010307A=CA2493476638APOBc.6561T= (p.Asp2187=)
c.5869+426T= (n.5869+426T=)
2g.21010307A>CCA43505136APOBc.6561T>G (p.Asp2187Glu)
c.5869+426T>G (n.5869+426T>G)
dbSNP
2g.21010307A>GCA425345654APOBc.6561T>C (p.Asp2187=)
c.5869+426T>C (n.5869+426T>C)
2g.21010307A>TCA346001481APOBc.6561T>A (p.Asp2187Glu)
c.5869+426T>A (n.5869+426T>A)
2g.21010308T>ACA346001482APOBc.6560A>T (p.Asp2187Val)
c.5869+425A>T (n.5869+425A>T)
dbSNP gnomAD v4
2g.21010308T>CCA346001483APOBc.6560A>G (p.Asp2187Gly)
c.5869+425A>G (n.5869+425A>G)
2g.21010308T>GCA346001484APOBc.6560A>C (p.Asp2187Ala)
c.5869+425A>C (n.5869+425A>C)
2g.21010308T=CA2493476639APOBc.6560A= (p.Asp2187=)
c.5869+425A= (n.5869+425A=)
2g.21010309C>ACA43505142APOBc.6559G>T (p.Asp2187Tyr)
c.5869+424G>T (n.5869+424G>T)
dbSNP
2g.21010309C=CA2493476640APOBc.6559G= (p.Asp2187=)
c.5869+424G= (n.5869+424G=)
2g.21010309C>GCA346001485APOBc.6559G>C (p.Asp2187His)
c.5869+424G>C (n.5869+424G>C)
2g.21010309C>TCA346001486APOBc.6559G>A (p.Asp2187Asn)
c.5869+424G>A (n.5869+424G>A)
dbSNP
2g.21010310T>ACA346001487APOBc.6558A>T (p.Lys2186Asn)
c.5869+423A>T (n.5869+423A>T)
2g.21010310T>CCA425345659APOBc.6558A>G (p.Lys2186=)
c.5869+423A>G (n.5869+423A>G)
gnomAD v4
2g.21010310T>GCA346001488APOBc.6558A>C (p.Lys2186Asn)
c.5869+423A>C (n.5869+423A>C)
2g.21010312delCA2576686891APOBc.6558del (p.Asp2187IlefsTer8)
c.5869+423del (n.5869+423del)
2g.21010311T>ACA346001489APOBc.6557A>T (p.Lys2186Ile)
c.5869+422A>T (n.5869+422A>T)
2g.21010311T>CCA346001490APOBc.6557A>G (p.Lys2186Arg)
c.5869+422A>G (n.5869+422A>G)
gnomAD v4
2g.21010311T>GCA346001491APOBc.6557A>C (p.Lys2186Thr)
c.5869+422A>C (n.5869+422A>C)
2g.21010312T>ACA346001494APOBc.6556A>T (p.Lys2186Ter)
c.5869+421A>T (n.5869+421A>T)
2g.21010312T>CCA346001492APOBc.6556A>G (p.Lys2186Glu)
c.5869+421A>G (n.5869+421A>G)
2g.21010312T>GCA346001493APOBc.6556A>C (p.Lys2186Gln)
c.5869+421A>C (n.5869+421A>C)
2g.21010313A>CCA346001495APOBc.6555T>G (p.Ile2185Met)
c.5869+420T>G (n.5869+420T>G)
2g.21010313A>GCA425345664APOBc.6555T>C (p.Ile2185=)
c.5869+420T>C (n.5869+420T>C)
2g.21010313A>TCA425345665APOBc.6555T>A (p.Ile2185=)
c.5869+420T>A (n.5869+420T>A)
2g.21010314A>CCA346001496APOBc.6554T>G (p.Ile2185Ser)
c.5869+419T>G (n.5869+419T>G)
2g.21010314A>GCA346001497APOBc.6554T>C (p.Ile2185Thr)
c.5869+419T>C (n.5869+419T>C)
2g.21010314A>TCA346001498APOBc.6554T>A (p.Ile2185Asn)
c.5869+419T>A (n.5869+419T>A)
2g.21010315T>ACA346001499APOBc.6553A>T (p.Ile2185Phe)
c.5869+418A>T (n.5869+418A>T)
2g.21010315T>CCA346001500APOBc.6553A>G (p.Ile2185Val)
c.5869+418A>G (n.5869+418A>G)
dbSNP gnomAD v3 gnomAD v4
2g.21010315T>GCA346001501APOBc.6553A>C (p.Ile2185Leu)
c.5869+418A>C (n.5869+418A>C)
COSMIC
2g.21010315T=CA2493476641APOBc.6553A= (p.Ile2185=)
c.5869+418A= (n.5869+418A=)
2g.21010316A>CCA346001502APOBc.6552T>G (p.Tyr2184Ter)
c.5869+417T>G (n.5869+417T>G)
2g.21010316A>GCA425345671APOBc.6552T>C (p.Tyr2184=)
c.5869+417T>C (n.5869+417T>C)
2g.21010316A>TCA346001503APOBc.6552T>A (p.Tyr2184Ter)
c.5869+417T>A (n.5869+417T>A)
2g.21010317T>ACA346001504APOBc.6551A>T (p.Tyr2184Phe)
c.5869+416A>T (n.5869+416A>T)
2g.21010317T>CCA063334APOBc.6551A>G (p.Tyr2184Cys)
c.5869+416A>G (n.5869+416A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010317T>GCA346001505APOBc.6551A>C (p.Tyr2184Ser)
c.5869+416A>C (n.5869+416A>C)
2g.21010317T=CA2493476642APOBc.6551A= (p.Tyr2184=)
c.5869+416A= (n.5869+416A=)
2g.21010318A=CA2493476643APOBc.6550T= (p.Tyr2184=)
c.5869+415T= (n.5869+415T=)
2g.21010318A>CCA346001507APOBc.6550T>G (p.Tyr2184Asp)
c.5869+415T>G (n.5869+415T>G)
gnomAD v4
2g.21010318A>GCA346001508APOBc.6550T>C (p.Tyr2184His)
c.5869+415T>C (n.5869+415T>C)
2g.21010318A>TCA346001506APOBc.6550T>A (p.Tyr2184Asn)
c.5869+415T>A (n.5869+415T>A)
dbSNP
2g.21010319C>ACA346001509APOBc.6549G>T (p.Gln2183His)
c.5869+414G>T (n.5869+414G>T)
gnomAD v4
2g.21010319C=CA2493476644APOBc.6549G= (p.Gln2183=)
c.5869+414G= (n.5869+414G=)
2g.21010319C>GCA346001510APOBc.6549G>C (p.Gln2183His)
c.5869+414G>C (n.5869+414G>C)
gnomAD v4
2g.21010319C>TCA425345673APOBc.6549G>A (p.Gln2183=)
c.5869+414G>A (n.5869+414G>A)
dbSNP gnomAD v2 gnomAD v4
2g.21010320T>ACA063326APOBc.6548A>T (p.Gln2183Leu)
c.5869+413A>T (n.5869+413A>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010320T>CCA346001511APOBc.6548A>G (p.Gln2183Arg)
c.5869+413A>G (n.5869+413A>G)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21010320T>GCA346001512APOBc.6548A>C (p.Gln2183Pro)
c.5869+413A>C (n.5869+413A>C)
2g.21010320T=CA2493476645APOBc.6548A= (p.Gln2183=)
c.5869+413A= (n.5869+413A=)
2g.21010321G>ACA346001513APOBc.6547C>T (p.Gln2183Ter)
c.5869+412C>T (n.5869+412C>T)
dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.21010321G>CCA346001514APOBc.6547C>G (p.Gln2183Glu)
c.5869+412C>G (n.5869+412C>G)
2g.21010321G=CA2493476646APOBc.6547C= (p.Gln2183=)
c.5869+412C= (n.5869+412C=)
2g.21010321G>TCA346001515APOBc.6547C>A (p.Gln2183Lys)
c.5869+412C>A (n.5869+412C>A)
gnomAD v4
2g.21010322A=CA2493476647APOBc.6546T= (p.Asp2182=)
c.5869+411T= (n.5869+411T=)
2g.21010322A>CCA346001516APOBc.6546T>G (p.Asp2182Glu)
c.5869+411T>G (n.5869+411T>G)
2g.21010322A>GCA425345676APOBc.6546T>C (p.Asp2182=)
c.5869+411T>C (n.5869+411T>C)
dbSNP gnomAD v4
2g.21010322A>TCA346001517APOBc.6546T>A (p.Asp2182Glu)
c.5869+411T>A (n.5869+411T>A)
2g.21010323T>ACA346001518APOBc.6545A>T (p.Asp2182Val)
c.5869+410A>T (n.5869+410A>T)
gnomAD v4
2g.21010323T>CCA346001519APOBc.6545A>G (p.Asp2182Gly)
c.5869+410A>G (n.5869+410A>G)
2g.21010323T>GCA346001520APOBc.6545A>C (p.Asp2182Ala)
c.5869+410A>C (n.5869+410A>C)
2g.21010324C>ACA346001523APOBc.6544G>T (p.Asp2182Tyr)
c.5869+409G>T (n.5869+409G>T)
dbSNP gnomAD v2 gnomAD v4
2g.21010324C=CA2493476648APOBc.6544G= (p.Asp2182=)
c.5869+409G= (n.5869+409G=)
2g.21010324C>GCA346001522APOBc.6544G>C (p.Asp2182His)
c.5869+409G>C (n.5869+409G>C)
2g.21010324C>TCA346001521APOBc.6544G>A (p.Asp2182Asn)
c.5869+409G>A (n.5869+409G>A)
2g.21010324_21010325delinsCACA2493476649APOBc.6543_6544delinsTG (p.Phe2181=)
c.5869+408_5869+409delinsTG (n.5869+408_5869+409delinsTG)
2g.21010325A>CCA346001524APOBc.6543T>G (p.Phe2181Leu)
c.5869+408T>G (n.5869+408T>G)
2g.21010325A>GCA425345682APOBc.6543T>C (p.Phe2181=)
c.5869+408T>C (n.5869+408T>C)
2g.21010325A>TCA346001525APOBc.6543T>A (p.Phe2181Leu)
c.5869+408T>A (n.5869+408T>A)
gnomAD v4
2g.21010327delCA531312753APOBc.6543del (p.Phe2181LeufsTer14)
c.5869+408del (n.5869+408del)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21010326A>CCA346001526APOBc.6542T>G (p.Phe2181Cys)
c.5869+407T>G (n.5869+407T>G)
2g.21010326A>GCA346001527APOBc.6542T>C (p.Phe2181Ser)
c.5869+407T>C (n.5869+407T>C)
gnomAD v4
2g.21010326A>TCA346001528APOBc.6542T>A (p.Phe2181Tyr)
c.5869+407T>A (n.5869+407T>A)
COSMIC
2g.21010327A>CCA346001529APOBc.6541T>G (p.Phe2181Val)
c.5869+406T>G (n.5869+406T>G)
2g.21010327A>GCA346001530APOBc.6541T>C (p.Phe2181Leu)
c.5869+406T>C (n.5869+406T>C)
gnomAD v4
2g.21010327A>TCA346001531APOBc.6541T>A (p.Phe2181Ile)
c.5869+406T>A (n.5869+406T>A)
2g.21010328T>ACA346001532APOBc.6540A>T (p.Gln2180His)
c.5869+405A>T (n.5869+405A>T)
2g.21010328T>CCA425345685APOBc.6540A>G (p.Gln2180=)
c.5869+405A>G (n.5869+405A>G)
COSMIC
2g.21010328T>GCA346001533APOBc.6540A>C (p.Gln2180His)
c.5869+405A>C (n.5869+405A>C)
2g.21010329delCA2580065002APOBc.6540del (p.Gln2180HisfsTer15)
c.5869+405del (n.5869+405del)
ClinVar gnomAD v4
2g.21010329T>ACA346001534APOBc.6539A>T (p.Gln2180Leu)
c.5869+404A>T (n.5869+404A>T)
2g.21010329T>CCA346001535APOBc.6539A>G (p.Gln2180Arg)
c.5869+404A>G (n.5869+404A>G)
2g.21010329T>GCA063322APOBc.6539A>C (p.Gln2180Pro)
c.5869+404A>C (n.5869+404A>C)
dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010329T=CA2493476650APOBc.6539A= (p.Gln2180=)
c.5869+404A= (n.5869+404A=)
2g.21010330G>ACA43505194APOBc.6538C>T (p.Gln2180Ter)
c.5869+403C>T (n.5869+403C>T)
dbSNP gnomAD v4
2g.21010330G>CCA346001537APOBc.6538C>G (p.Gln2180Glu)
c.5869+403C>G (n.5869+403C>G)
2g.21010330G=CA2493476651APOBc.6538C= (p.Gln2180=)
c.5869+403C= (n.5869+403C=)
2g.21010330G>TCA346001536APOBc.6538C>A (p.Gln2180Lys)
c.5869+403C>A (n.5869+403C>A)
gnomAD v4
2g.21010331T>ACA425345687APOBc.6537A>T (p.Ile2179=)
c.5869+402A>T (n.5869+402A>T)
2g.21010331T>CCA346001538APOBc.6537A>G (p.Ile2179Met)
c.5869+402A>G (n.5869+402A>G)
COSMIC
2g.21010331T>GCA425345688APOBc.6537A>C (p.Ile2179=)
c.5869+402A>C (n.5869+402A>C)
2g.21010332A>CCA346001540APOBc.6536T>G (p.Ile2179Arg)
c.5869+401T>G (n.5869+401T>G)
2g.21010332A>GCA346001539APOBc.6536T>C (p.Ile2179Thr)
c.5869+401T>C (n.5869+401T>C)
2g.21010332A>TCA346001541APOBc.6536T>A (p.Ile2179Lys)
c.5869+401T>A (n.5869+401T>A)
2g.21010333T>ACA346001542APOBc.6535A>T (p.Ile2179Leu)
c.5869+400A>T (n.5869+400A>T)
2g.21010333T>CCA346001543APOBc.6535A>G (p.Ile2179Val)
c.5869+400A>G (n.5869+400A>G)
gnomAD v4 COSMIC
2g.21010333T>GCA346001544APOBc.6535A>C (p.Ile2179Leu)
c.5869+400A>C (n.5869+400A>C)
2g.21010334C>ACA346001545APOBc.6534G>T (p.Met2178Ile)
c.5869+399G>T (n.5869+399G>T)
2g.21010334C=CA2493476652APOBc.6534G= (p.Met2178=)
c.5869+399G= (n.5869+399G=)
2g.21010334C>GCA346001546APOBc.6534G>C (p.Met2178Ile)
c.5869+399G>C (n.5869+399G>C)
2g.21010334C>TCA346001547APOBc.6534G>A (p.Met2178Ile)
c.5869+399G>A (n.5869+399G>A)
dbSNP gnomAD v2 COSMIC
2g.21010335A=CA2493476653APOBc.6533T= (p.Met2178=)
c.5869+398T= (n.5869+398T=)
2g.21010335A>CCA346001550APOBc.6533T>G (p.Met2178Arg)
c.5869+398T>G (n.5869+398T>G)
2g.21010335A>GCA346001548APOBc.6533T>C (p.Met2178Thr)
c.5869+398T>C (n.5869+398T>C)
dbSNP
2g.21010335A>TCA346001549APOBc.6533T>A (p.Met2178Lys)
c.5869+398T>A (n.5869+398T>A)
2g.21010336T>ACA346001551APOBc.6532A>T (p.Met2178Leu)
c.5869+397A>T (n.5869+397A>T)
COSMIC
2g.21010336T>CCA43505205APOBc.6532A>G (p.Met2178Val)
c.5869+397A>G (n.5869+397A>G)
dbSNP gnomAD v4
2g.21010336T>GCA346001552APOBc.6532A>C (p.Met2178Leu)
c.5869+397A>C (n.5869+397A>C)
2g.21010336T=CA2493476654APOBc.6532A= (p.Met2178=)
c.5869+397A= (n.5869+397A=)
2g.21010337A=CA2493476655APOBc.6531T= (p.Tyr2177=)
c.5869+396T= (n.5869+396T=)
2g.21010337A>CCA346001553APOBc.6531T>G (p.Tyr2177Ter)
c.5869+396T>G (n.5869+396T>G)
2g.21010337A>GCA425345690APOBc.6531T>C (p.Tyr2177=)
c.5869+396T>C (n.5869+396T>C)
ClinVar dbSNP COSMIC
2g.21010337A>TCA346001554APOBc.6531T>A (p.Tyr2177Ter)
c.5869+396T>A (n.5869+396T>A)
2g.21010338T>ACA346001555APOBc.6530A>T (p.Tyr2177Phe)
c.5869+395A>T (n.5869+395A>T)
2g.21010338T>CCA346001557APOBc.6530A>G (p.Tyr2177Cys)
c.5869+395A>G (n.5869+395A>G)
dbSNP gnomAD v2 gnomAD v4 COSMIC
2g.21010338T>GCA346001556APOBc.6530A>C (p.Tyr2177Ser)
c.5869+395A>C (n.5869+395A>C)
ClinVar dbSNP gnomAD v4
2g.21010338T=CA2493476656APOBc.6530A= (p.Tyr2177=)
c.5869+395A= (n.5869+395A=)
2g.21010339A=CA2493476657APOBc.6529T= (p.Tyr2177=)
c.5869+394T= (n.5869+394T=)
2g.21010339A>CCA346001558APOBc.6529T>G (p.Tyr2177Asp)
c.5869+394T>G (n.5869+394T>G)
2g.21010339A>GCA43505221APOBc.6529T>C (p.Tyr2177His)
c.5869+394T>C (n.5869+394T>C)
dbSNP
2g.21010339A>TCA346001559APOBc.6529T>A (p.Tyr2177Asn)
c.5869+394T>A (n.5869+394T>A)
2g.21010340T>ACA425345692APOBc.6528A>T (p.Thr2176=)
c.5869+393A>T (n.5869+393A>T)
2g.21010340T>CCA425345693APOBc.6528A>G (p.Thr2176=)
c.5869+393A>G (n.5869+393A>G)
COSMIC
2g.21010340T>GCA425345694APOBc.6528A>C (p.Thr2176=)
c.5869+393A>C (n.5869+393A>C)
2g.21010341G>ACA346001560APOBc.6527C>T (p.Thr2176Ile)
c.5869+392C>T (n.5869+392C>T)
gnomAD v4
2g.21010341G>CCA346001561APOBc.6527C>G (p.Thr2176Arg)
c.5869+392C>G (n.5869+392C>G)
2g.21010341G>TCA346001562APOBc.6527C>A (p.Thr2176Lys)
c.5869+392C>A (n.5869+392C>A)
2g.21010342T>ACA346001563APOBc.6526A>T (p.Thr2176Ser)
c.5869+391A>T (n.5869+391A>T)
2g.21010342T>CCA346001564APOBc.6526A>G (p.Thr2176Ala)
c.5869+391A>G (n.5869+391A>G)
COSMIC
2g.21010342T>GCA346001565APOBc.6526A>C (p.Thr2176Pro)
c.5869+391A>C (n.5869+391A>C)
2g.21010343C>ACA346001566APOBc.6525G>T (p.Gln2175His)
c.5869+390G>T (n.5869+390G>T)
2g.21010343C>GCA346001567APOBc.6525G>C (p.Gln2175His)
c.5869+390G>C (n.5869+390G>C)
2g.21010343C>TCA425345698APOBc.6525G>A (p.Gln2175=)
c.5869+390G>A (n.5869+390G>A)
gnomAD v4
2g.21010344T>ACA346001570APOBc.6524A>T (p.Gln2175Leu)
c.5869+389A>T (n.5869+389A>T)
2g.21010344T>CCA346001569APOBc.6524A>G (p.Gln2175Arg)
c.5869+389A>G (n.5869+389A>G)
dbSNP gnomAD v2 gnomAD v4
2g.21010344T>GCA346001568APOBc.6524A>C (p.Gln2175Pro)
c.5869+389A>C (n.5869+389A>C)
2g.21010344T=CA2493476658APOBc.6524A= (p.Gln2175=)
c.5869+389A= (n.5869+389A=)
2g.21010345G>ACA346001573APOBc.6523C>T (p.Gln2175Ter)
c.5869+388C>T (n.5869+388C>T)
gnomAD v4
2g.21010345G>CCA346001571APOBc.6523C>G (p.Gln2175Glu)
c.5869+388C>G (n.5869+388C>G)
dbSNP
2g.21010345G=CA2493476659APOBc.6523C= (p.Gln2175=)
c.5869+388C= (n.5869+388C=)
2g.21010345G>TCA346001572APOBc.6523C>A (p.Gln2175Lys)
c.5869+388C>A (n.5869+388C>A)
gnomAD v4
2g.21010346C>ACA425345703APOBc.6522G>T (p.Leu2174=)
c.5869+387G>T (n.5869+387G>T)
ClinVar dbSNP gnomAD v2 gnomAD v4
2g.21010346C=CA2493476660APOBc.6522G= (p.Leu2174=)
c.5869+387G= (n.5869+387G=)
2g.21010346C>GCA425345702APOBc.6522G>C (p.Leu2174=)
c.5869+387G>C (n.5869+387G>C)
2g.21010346C>TCA425345701APOBc.6522G>A (p.Leu2174=)
c.5869+387G>A (n.5869+387G>A)
COSMIC
2g.21010347A>CCA346001574APOBc.6521T>G (p.Leu2174Arg)
c.5869+386T>G (n.5869+386T>G)
2g.21010347A>GCA346001575APOBc.6521T>C (p.Leu2174Pro)
c.5869+386T>C (n.5869+386T>C)
gnomAD v4
2g.21010347A>TCA346001576APOBc.6521T>A (p.Leu2174Gln)
c.5869+386T>A (n.5869+386T>A)
2g.21010348G>ACA425345705APOBc.6520C>T (p.Leu2174=)
c.5869+385C>T (n.5869+385C>T)
2g.21010348G>CCA346001577APOBc.6520C>G (p.Leu2174Val)
c.5869+385C>G (n.5869+385C>G)
2g.21010348G>TCA346001578APOBc.6520C>A (p.Leu2174Met)
c.5869+385C>A (n.5869+385C>A)
2g.21010349T>ACA346001579APOBc.6519A>T (p.Gln2173His)
c.5869+384A>T (n.5869+384A>T)
2g.21010349T>CCA425345708APOBc.6519A>G (p.Gln2173=)
c.5869+384A>G (n.5869+384A>G)
dbSNP
2g.21010349T>GCA346001580APOBc.6519A>C (p.Gln2173His)
c.5869+384A>C (n.5869+384A>C)
COSMIC
2g.21010349T=CA2493476661APOBc.6519A= (p.Gln2173=)
c.5869+384A= (n.5869+384A=)
2g.21010350T>ACA346001581APOBc.6518A>T (p.Gln2173Leu)
c.5869+383A>T (n.5869+383A>T)
2g.21010350T>CCA346001582APOBc.6518A>G (p.Gln2173Arg)
c.5869+383A>G (n.5869+383A>G)
2g.21010350T>GCA346001583APOBc.6518A>C (p.Gln2173Pro)
c.5869+383A>C (n.5869+383A>C)
gnomAD v4
2g.21010351G>ACA346001585APOBc.6517C>T (p.Gln2173Ter)
c.5869+382C>T (n.5869+382C>T)
2g.21010351G>CCA063313APOBc.6517C>G (p.Gln2173Glu)
c.5869+382C>G (n.5869+382C>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010351G=CA2493476662APOBc.6517C= (p.Gln2173=)
c.5869+382C= (n.5869+382C=)
2g.21010351G>TCA346001584APOBc.6517C>A (p.Gln2173Lys)
c.5869+382C>A (n.5869+382C>A)
2g.21010352A>CCA425345710APOBc.6516T>G (p.Ser2172=)
c.5869+381T>G (n.5869+381T>G)
2g.21010352A>GCA425345711APOBc.6516T>C (p.Ser2172=)
c.5869+381T>C (n.5869+381T>C)
2g.21010352A>TCA425345712APOBc.6516T>A (p.Ser2172=)
c.5869+381T>A (n.5869+381T>A)
2g.21010353G>ACA346001586APOBc.6515C>T (p.Ser2172Phe)
c.5869+380C>T (n.5869+380C>T)
dbSNP
2g.21010353G>CCA346001587APOBc.6515C>G (p.Ser2172Cys)
c.5869+380C>G (n.5869+380C>G)
2g.21010353G=CA2493476663APOBc.6515C= (p.Ser2172=)
c.5869+380C= (n.5869+380C=)
2g.21010353G>TCA346001588APOBc.6515C>A (p.Ser2172Tyr)
c.5869+380C>A (n.5869+380C>A)
gnomAD v4
2g.21010354A=CA2493476664APOBc.6514T= (p.Ser2172=)
c.5869+379T= (n.5869+379T=)
2g.21010354A>CCA346001589APOBc.6514T>G (p.Ser2172Ala)
c.5869+379T>G (n.5869+379T>G)
2g.21010354A>GCA346001590APOBc.6514T>C (p.Ser2172Pro)
c.5869+379T>C (n.5869+379T>C)
2g.21010354A>TCA346001591APOBc.6514T>A (p.Ser2172Thr)
c.5869+379T>A (n.5869+379T>A)
dbSNP
2g.21010355T>ACA425345715APOBc.6513A>T (p.Leu2171=)
c.5869+378A>T (n.5869+378A>T)
2g.21010355T>CCA063308APOBc.6513A>G (p.Leu2171=)
c.5869+378A>G (n.5869+378A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
2g.21010355T>GCA425345717APOBc.6513A>C (p.Leu2171=)
c.5869+378A>C (n.5869+378A>C)
dbSNP
2g.21010355T=CA2493476665APOBc.6513A= (p.Leu2171=)
c.5869+378A= (n.5869+378A=)
2g.21010356A=CA2493476666APOBc.6512T= (p.Leu2171=)
c.5869+377T= (n.5869+377T=)
2g.21010356A>CCA346001592APOBc.6512T>G (p.Leu2171Arg)
c.5869+377T>G (n.5869+377T>G)
gnomAD v4
2g.21010356A>GCA346001593APOBc.6512T>C (p.Leu2171Pro)
c.5869+377T>C (n.5869+377T>C)
dbSNP gnomAD v4
2g.21010356A>TCA346001594APOBc.6512T>A (p.Leu2171Gln)
c.5869+377T>A (n.5869+377T>A)
2g.21010357G>ACA425345720APOBc.6511C>T (p.Leu2171=)
c.5869+376C>T (n.5869+376C>T)
gnomAD v4
2g.21010357G>CCA346001595APOBc.6511C>G (p.Leu2171Val)
c.5869+376C>G (n.5869+376C>G)
gnomAD v4
2g.21010357G=CA2493476667APOBc.6511C= (p.Leu2171=)
c.5869+376C= (n.5869+376C=)
2g.21010357G>TCA346001596APOBc.6511C>A (p.Leu2171Ile)
c.5869+376C>A (n.5869+376C>A)
dbSNP gnomAD v2 gnomAD v4
2g.21010358T>ACA43505233APOBc.6510A>T (p.Lys2170Asn)
c.5869+375A>T (n.5869+375A>T)
dbSNP gnomAD v3 gnomAD v4
2g.21010358T>CCA425345721APOBc.6510A>G (p.Lys2170=)
c.5869+375A>G (n.5869+375A>G)
2g.21010358T>GCA346001597APOBc.6510A>C (p.Lys2170Asn)
c.5869+375A>C (n.5869+375A>C)
2g.21010358T=CA2493476668APOBc.6510A= (p.Lys2170=)
c.5869+375A= (n.5869+375A=)

Number of alleles fetched