Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.224503653T>A | CA350826872 | CUL3 | c.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 |
2 | g.224503653T>C | CA269962 | CUL3 | c.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 |