Chr Mutation (hg38) CAid Gene Transcript Linkouts
9g.35065364G>CCA277489VCPc.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
9g.35065364G>TCA373289661VCPc.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
9g.35065364G>ACA254398VCPc.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

Number of alleles fetched