Table 3.
Mutation genotype | Mutation type | Exon | Codon change | Amino acid change | Case ID/Cell line |
---|---|---|---|---|---|
Colorectal cancer tissues | |||||
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 | |||||
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 |
ASB3, ankyrin repeat and suppressor of cytokine signaling (SOCS) box protein 3
The nucleotides in bold indicate the one mutated
a CDS coding domain sequence; A, T, C, G, four types of nucleotides; R = A/G; Y = C/T; W = A/T; K = G/T
bamino acid codon