Table 2.
No. | Patient | EX05 | EX06 | EX07 | EX08 | EX09 | Codon change | Base substitution | (type) | AA change | MSI |
---|---|---|---|---|---|---|---|---|---|---|---|
1 | IC628 | 273 | CGT → CAT | G:C → A:T | TS | Arg → His | N | ||||
2 | IC630 | 196 | CGA → TGA | G:C → A:T | TS | Arg → stop | A | ||||
3 | IC634 | 306 | CGA → TGA | G:C → A:T | TS | Arg → stop | N | ||||
4 | IC668 | 193 | CAT → CGT | A:T → G:C | TS | His → Arg | N | ||||
5 | IC669 | 175 | CGC → CAC | G:C → A:T | TS | Arg → His | A | ||||
6 | IC673 | 176 | TGC → AGC | A:T → T:A | TV | Cys → Ser | N | ||||
7 | IC674 | 285 | GAG → AAG | G:C → A:T | TS | Glu → Lys | N | ||||
8 | IC680 | ND | 255 | ATC → ACC | A:T → G:C | TS | Ile → Thr | A | |||
9 | IC693 | 179 | CAT → CTT | A:T → T:A | TV | His → Leu | A | ||||
10 | IC694 | 273 | CGT → CAT | G:C → A:T | TS | Arg → His | A | ||||
11 | IC711 | 239 | AAC → GAC | A:T → G:C | TS | Asn → Asp | N | ||||
12 | IC721 | 175 | CGC → CAC | G:C → A:T | TS | Arg → His | A | ||||
13 | IC748 | 190 | ND | CCT → CTT | G:C → A:T | TS | Pro → Leu | A | |||
14 | IC754 | 196 | CGA → CCA | G:C → C:G | TV | Arg → Pro | N | ||||
15 | IC763 | 151 | CCC → CAC | G:C → T:A | TV | Pro → His | N | ||||
16 | IC772 | 175 | CGC → CAC | G:C → A:T | TS | Arg → His | A | ||||
17 | IC778 | 175 | ND | CGC → CAC | G:C → A:T | TS | Arg → His | N | |||
18 | IC784 | 214 | ND | ND | CAT → CGT | A:T → G:C | TS | His → Arg | A | ||
19 | IC808 | 205 | TAT → GAT | A:T → C:G | TV | Tyr → Asp | A | ||||
20 | IC812 | 190 | CCT → CTT | G:C → A:T | TS | Pro → Leu | N | ||||
21 | IC816 | 273 | CGT → CAT | G:C → A:T | TS | Arg → His | A | ||||
22 | IC819 | 248 | CGG → CAG | G:C → A:T | TS | Arg → Gln | N | ||||
23 | IC860 | 273 | CGT → CAT | G:C → A:T | TS | Arg → His | A |
MSI, microsatellite instability; N, negative; A, Type A MSI; TS, transition; TV, transversion; ND, not determined. Bold codon numbers indicate the acknowledged hot-spots for mutation.