Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.21010518T>ACA346001955APOBc.6350A>T (p.Lys2117Ile)
c.5869+215A>T (n.5869+215A>T)
2g.21010518T>CCA346001956APOBc.6350A>G (p.Lys2117Arg)
c.5869+215A>G (n.5869+215A>G)
2g.21010518T>GCA346001957APOBc.6350A>C (p.Lys2117Thr)
c.5869+215A>C (n.5869+215A>C)
2g.21010519T>ACA346001960APOBc.6349A>T (p.Lys2117Ter)
c.5869+214A>T (n.5869+214A>T)
2g.21010519T>CCA346001958APOBc.6349A>G (p.Lys2117Glu)
c.5869+214A>G (n.5869+214A>G)
gnomAD v4
2g.21010519T>GCA346001959APOBc.6349A>C (p.Lys2117Gln)
c.5869+214A>C (n.5869+214A>C)
2g.21010520T>ACA425346111APOBc.6348A>T (p.Gly2116=)
c.5869+213A>T (n.5869+213A>T)
2g.21010520T>CCA063129APOBc.6348A>G (p.Gly2116=)
c.5869+213A>G (n.5869+213A>G)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010520T>GCA425346112APOBc.6348A>C (p.Gly2116=)
c.5869+213A>C (n.5869+213A>C)
2g.21010520T=CA2493476731APOBc.6348A= (p.Gly2116=)
c.5869+213A= (n.5869+213A=)
2g.21010521C>ACA346001961APOBc.6347G>T (p.Gly2116Val)
c.5869+212G>T (n.5869+212G>T)
2g.21010521C>GCA346001962APOBc.6347G>C (p.Gly2116Ala)
c.5869+212G>C (n.5869+212G>C)
2g.21010521C>TCA346001963APOBc.6347G>A (p.Gly2116Glu)
c.5869+212G>A (n.5869+212G>A)
COSMIC
2g.21010522C>ACA346001964APOBc.6346G>T (p.Gly2116Ter)
c.5869+211G>T (n.5869+211G>T)
2g.21010522C>GCA346001965APOBc.6346G>C (p.Gly2116Arg)
c.5869+211G>C (n.5869+211G>C)
2g.21010522C>TCA346001966APOBc.6346G>A (p.Gly2116Arg)
c.5869+211G>A (n.5869+211G>A)
2g.21010523C>ACA425346116APOBc.6345G>T (p.Leu2115=)
c.5869+210G>T (n.5869+210G>T)
2g.21010523C=CA2493476732APOBc.6345G= (p.Leu2115=)
c.5869+210G= (n.5869+210G=)
2g.21010523C>GCA425346118APOBc.6345G>C (p.Leu2115=)
c.5869+210G>C (n.5869+210G>C)
dbSNP gnomAD v3 gnomAD v4
2g.21010523C>TCA425346119APOBc.6345G>A (p.Leu2115=)
c.5869+210G>A (n.5869+210G>A)
COSMIC
2g.21010524A>CCA346001967APOBc.6344T>G (p.Leu2115Arg)
c.5869+209T>G (n.5869+209T>G)
2g.21010524A>GCA346001968APOBc.6344T>C (p.Leu2115Pro)
c.5869+209T>C (n.5869+209T>C)
2g.21010524A>TCA346001969APOBc.6344T>A (p.Leu2115Gln)
c.5869+209T>A (n.5869+209T>A)
2g.21010525G>ACA425346121APOBc.6343C>T (p.Leu2115=)
c.5869+208C>T (n.5869+208C>T)
2g.21010525G>CCA346001970APOBc.6343C>G (p.Leu2115Val)
c.5869+208C>G (n.5869+208C>G)
2g.21010525G>TCA346001971APOBc.6343C>A (p.Leu2115Met)
c.5869+208C>A (n.5869+208C>A)
2g.21010525_21010530delCA2658056054APOBc.6338_6343del (p.Ala2113_Leu2115delinsVal)
c.5869+203_5869+208del (n.5869+203_5869+208del)
gnomAD v4
2g.21010526G>ACA063120APOBc.6342C>T (p.Ala2114=)
c.5869+207C>T (n.5869+207C>T)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
2g.21010526G>CCA425346130APOBc.6342C>G (p.Ala2114=)
c.5869+207C>G (n.5869+207C>G)
2g.21010526G=CA2493476733APOBc.6342C= (p.Ala2114=)
c.5869+207C= (n.5869+207C=)
2g.21010526G>TCA425346131APOBc.6342C>A (p.Ala2114=)
c.5869+207C>A (n.5869+207C>A)
2g.21010527G>ACA346001972APOBc.6341C>T (p.Ala2114Val)
c.5869+206C>T (n.5869+206C>T)
dbSNP gnomAD v3 gnomAD v4
2g.21010527G>CCA346001974APOBc.6341C>G (p.Ala2114Gly)
c.5869+206C>G (n.5869+206C>G)
2g.21010527G=CA2493476734APOBc.6341C= (p.Ala2114=)
c.5869+206C= (n.5869+206C=)
2g.21010527G>TCA346001973APOBc.6341C>A (p.Ala2114Asp)
c.5869+206C>A (n.5869+206C>A)
2g.21010528C>ACA346001975APOBc.6340G>T (p.Ala2114Ser)
c.5869+205G>T (n.5869+205G>T)
ClinVar dbSNP gnomAD v4
2g.21010528C=CA2493476735APOBc.6340G= (p.Ala2114=)
c.5869+205G= (n.5869+205G=)
2g.21010528C>GCA43505461APOBc.6340G>C (p.Ala2114Pro)
c.5869+205G>C (n.5869+205G>C)
dbSNP
2g.21010528C>TCA346001976APOBc.6340G>A (p.Ala2114Thr)
c.5869+205G>A (n.5869+205G>A)
2g.21010529T>ACA425346134APOBc.6339A>T (p.Ala2113=)
c.5869+204A>T (n.5869+204A>T)
2g.21010529T>CCA425346137APOBc.6339A>G (p.Ala2113=)
c.5869+204A>G (n.5869+204A>G)
2g.21010529T>GCA425346140APOBc.6339A>C (p.Ala2113=)
c.5869+204A>C (n.5869+204A>C)
2g.21010530G>ACA43505462APOBc.6338C>T (p.Ala2113Val)
c.5869+203C>T (n.5869+203C>T)
dbSNP gnomAD v4 COSMIC
2g.21010530G>CCA346001977APOBc.6338C>G (p.Ala2113Gly)
c.5869+203C>G (n.5869+203C>G)
2g.21010530G=CA2493476736APOBc.6338C= (p.Ala2113=)
c.5869+203C= (n.5869+203C=)
2g.21010530G>TCA346001978APOBc.6338C>A (p.Ala2113Glu)
c.5869+203C>A (n.5869+203C>A)
dbSNP gnomAD v4
2g.21010531C>ACA346001979APOBc.6337G>T (p.Ala2113Ser)
c.5869+202G>T (n.5869+202G>T)
gnomAD v4
2g.21010531C=CA2493476737APOBc.6337G= (p.Ala2113=)
c.5869+202G= (n.5869+202G=)
2g.21010531C>GCA346001980APOBc.6337G>C (p.Ala2113Pro)
c.5869+202G>C (n.5869+202G>C)
2g.21010531C>TCA063112APOBc.6337G>A (p.Ala2113Thr)
c.5869+202G>A (n.5869+202G>A)
dbSNP ExAC gnomAD v2 gnomAD v4

Number of alleles fetched