Chr Mutation (hg38) CAid Gene Transcript Linkouts
11g.116790940G>ACA6289100APOA5c.289C>T (p.Gln97Ter)
c.373C>T (p.Gln125Ter)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790940G>CCA382739471APOA5c.289C>G (p.Gln97Glu)
c.373C>G (p.Gln125Glu)
11g.116790940G=CA2002741121APOA5c.289C= (p.Gln97=)
c.373C= (p.Gln125=)
11g.116790940G>TCA6289101APOA5c.289C>A (p.Gln97Lys)
c.373C>A (p.Gln125Lys)
dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC
11g.116790941C>ACA477047890APOA5c.288G>T (p.Leu96=)
c.372G>T (p.Leu124=)
11g.116790941C>GCA477047892APOA5c.288G>C (p.Leu96=)
c.372G>C (p.Leu124=)
11g.116790941C>TCA477047891APOA5c.288G>A (p.Leu96=)
c.372G>A (p.Leu124=)
11g.116790942A=CA2002741123APOA5c.287T= (p.Leu96=)
c.371T= (p.Leu124=)
11g.116790942A>CCA382739474APOA5c.287T>G (p.Leu96Arg)
c.371T>G (p.Leu124Arg)
dbSNP
11g.116790942A>GCA382739477APOA5c.287T>C (p.Leu96Pro)
c.371T>C (p.Leu124Pro)
11g.116790942A>TCA382739486APOA5c.287T>A (p.Leu96Gln)
c.371T>A (p.Leu124Gln)
11g.116790943G>ACA477047893APOA5c.286C>T (p.Leu96=)
c.370C>T (p.Leu124=)
ClinVar
11g.116790943G>CCA382739490APOA5c.286C>G (p.Leu96Val)
c.370C>G (p.Leu124Val)
11g.116790943G>TCA382739491APOA5c.286C>A (p.Leu96Met)
c.370C>A (p.Leu124Met)
11g.116790944C>ACA382739492APOA5c.285G>T (p.Gln95His)
c.369G>T (p.Gln123His)
11g.116790944C>GCA382739493APOA5c.285G>C (p.Gln95His)
c.369G>C (p.Gln123His)
11g.116790944C>TCA477047897APOA5c.285G>A (p.Gln95=)
c.369G>A (p.Gln123=)
11g.116790945T>ACA382739495APOA5c.284A>T (p.Gln95Leu)
c.368A>T (p.Gln123Leu)
11g.116790945T>CCA382739498APOA5c.284A>G (p.Gln95Arg)
c.368A>G (p.Gln123Arg)
11g.116790945T>GCA382739500APOA5c.284A>C (p.Gln95Pro)
c.368A>C (p.Gln123Pro)
11g.116790946G>ACA6289102APOA5c.283C>T (p.Gln95Ter)
c.367C>T (p.Gln123Ter)
dbSNP ExAC gnomAD v2 gnomAD v4
11g.116790946G>CCA382739501APOA5c.283C>G (p.Gln95Glu)
c.367C>G (p.Gln123Glu)
11g.116790946G=CA2002741126APOA5c.283C= (p.Gln95=)
c.367C= (p.Gln123=)
11g.116790946G>TCA382739503APOA5c.283C>A (p.Gln95Lys)
c.367C>A (p.Gln123Lys)
11g.116790947C>ACA477047899APOA5c.282G>T (p.Arg94=)
c.366G>T (p.Arg122=)
11g.116790947C=CA2002741128APOA5c.282G= (p.Arg94=)
c.366G= (p.Arg122=)
11g.116790947C>GCA477047901APOA5c.282G>C (p.Arg94=)
c.366G>C (p.Arg122=)
11g.116790947C>TCA477047902APOA5c.282G>A (p.Arg94=)
c.366G>A (p.Arg122=)
dbSNP gnomAD v4
11g.116790948C>ACA6289103APOA5c.281G>T (p.Arg94Leu)
c.365G>T (p.Arg122Leu)
dbSNP ExAC gnomAD v2
11g.116790948C=CA2002741133APOA5c.281G= (p.Arg94=)
c.365G= (p.Arg122=)
11g.116790948C>GCA382739509APOA5c.281G>C (p.Arg94Pro)
c.365G>C (p.Arg122Pro)
dbSNP gnomAD v3 gnomAD v4
11g.116790948C>TCA382739507APOA5c.281G>A (p.Arg94Gln)
c.365G>A (p.Arg122Gln)
ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790949G>ACA6289104APOA5c.280C>T (p.Arg94Trp)
c.364C>T (p.Arg122Trp)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790949G>CCA382739518APOA5c.280C>G (p.Arg94Gly)
c.364C>G (p.Arg122Gly)
11g.116790949G=CA2002741138APOA5c.280C= (p.Arg94=)
c.364C= (p.Arg122=)
11g.116790949G>TCA477047905APOA5c.280C>A (p.Arg94=)
c.364C>A (p.Arg122=)
11g.116790950C>ACA477047906APOA5c.279G>T (p.Arg93=)
c.363G>T (p.Arg121=)
11g.116790950C>GCA477047907APOA5c.279G>C (p.Arg93=)
c.363G>C (p.Arg121=)
11g.116790950C>TCA477047908APOA5c.279G>A (p.Arg93=)
c.363G>A (p.Arg121=)
11g.116790951C>ACA382739520APOA5c.278G>T (p.Arg93Leu)
c.362G>T (p.Arg121Leu)
dbSNP gnomAD v4
11g.116790951C=CA2002741142APOA5c.278G= (p.Arg93=)
c.362G= (p.Arg121=)
11g.116790951C>GCA382739527APOA5c.278G>C (p.Arg93Pro)
c.362G>C (p.Arg121Pro)
11g.116790951C>TCA6289105APOA5c.278G>A (p.Arg93Gln)
c.362G>A (p.Arg121Gln)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
11g.116790952G>ACA229338148APOA5c.277C>T (p.Arg93Trp)
c.361C>T (p.Arg121Trp)
dbSNP gnomAD v2 gnomAD v4
11g.116790952G>CCA382739532APOA5c.277C>G (p.Arg93Gly)
c.361C>G (p.Arg121Gly)
11g.116790952G=CA2002741145APOA5c.277C= (p.Arg93=)
c.361C= (p.Arg121=)
11g.116790952G>TCA229338135APOA5c.277C>A (p.Arg93=)
c.361C>A (p.Arg121=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
11g.116790953C>ACA382739535APOA5c.276G>T (p.Met92Ile)
c.360G>T (p.Met120Ile)
11g.116790953C=CA2002741149APOA5c.276G= (p.Met92=)
c.360G= (p.Met120=)
11g.116790953C>GCA382739536APOA5c.276G>C (p.Met92Ile)
c.360G>C (p.Met120Ile)

Number of alleles fetched