Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.35065364G>C | CA277489 | VCP | c.463C>G (p.Arg155Gly) c.328C>G (p.Arg110Gly) n.735C>G n.809C>G c.457C>G (p.Arg153Gly) c.*434C>G (n.*434C>G) n.733C>G n.784C>G c.18C>G c.185C>G (p.Pro62Arg) c.215C>G c.629C>G n.659C>G | ClinVar dbSNP |
9 | g.35065364G>T | CA373289661 | VCP | c.463C>A (p.Arg155Ser) c.328C>A (p.Arg110Ser) n.735C>A n.809C>A c.457C>A (p.Arg153Ser) c.*434C>A (n.*434C>A) n.733C>A n.784C>A c.18C>A c.185C>A (p.Pro62Gln) c.215C>A c.629C>A n.659C>A | ClinVar dbSNP |
9 | g.35065364G>A | CA254398 | VCP | c.463C>T (p.Arg155Cys) c.328C>T (p.Arg110Cys) n.735C>T n.809C>T c.457C>T (p.Arg153Cys) c.*434C>T (n.*434C>T) n.733C>T n.784C>T c.18C>T c.185C>T (p.Pro62Leu) c.215C>T c.629C>T n.659C>T | ClinVar dbSNP COSMIC |