Mutation genotype | Mutation type | Exon | Codon change | Amino acid change | Case ID/Cell line |
---|---|---|---|---|---|
Colorectal cancer tissues | Â | ||||
 CDS 21C→Ga | Nonsense | Exon 2 | TAC→TAG b | Y7stop | C56 |
 chr2:53810098 G→C | Splice-site | Exon 3/Intron | – | – | C53 |
 CDS 404G→R | Missense | Exon 4 | GGA→GAA | G135E | S78, S64 |
 CDS 1084C→Y | Missense | Exon 8 | CGC→TGC | R362C | S35 |
 CDS 1016A→W | Missense | Exon 8 | AAA→ATA | K339I | S12, S61, S64 |
Colorectal cancer cell lines | Â | ||||
 CDS 471A→T | Missense | Exon 5 | GAA→GAT | E157D | HCT116 |
 CDS 471A→W | Missense | Exon 5 | GAA→GAT | E157D | HT-29 |
 CDS 24G→R | Synonymous | Exon 2 | GCG→GCA | Non | DLD-1 |
 CDS 25G→K | Missense | Exon 2 | GAC→TAC | D9Y | DLD-1 |
 CDS 154T→Y | Missense | Exon 2 | TAT→CAT | Y52H | DLD-1 |
 CDS 922G→R | Missensee | Exon 7 | GCC→ACC | A308T | DLD-1 |