Chr Mutation (hg38) CAid Gene Transcript Linkouts
2g.224503653T>ACA350826872CUL3c.1376A>T (p.Lys459Met)
c.1178A>T (p.Lys393Met)
c.1304A>T (p.Lys435Met)
n.672A>T
c.98A>T (p.Lys33Met)
c.1394A>T (p.Lys465Met)
c.1343A>T (p.Lys448Met)
c.1229A>T (p.Lys410Met)
c.1334A>T (p.Lys445Met)
c.1184A>T (p.Lys395Met)
c.1076A>T (p.Lys359Met)
dbSNP COSMIC
2g.224503653T>CCA269962CUL3c.1376A>G (p.Lys459Arg)
c.1178A>G (p.Lys393Arg)
c.1304A>G (p.Lys435Arg)
n.672A>G
c.98A>G (p.Lys33Arg)
c.1394A>G (p.Lys465Arg)
c.1343A>G (p.Lys448Arg)
c.1229A>G (p.Lys410Arg)
c.1334A>G (p.Lys445Arg)
c.1184A>G (p.Lys395Arg)
c.1076A>G (p.Lys359Arg)
ClinVar dbSNP gnomAD v4

Number of alleles fetched