Table II.
Nucleotides at positions | No. of substitutionsa | |||||||
Genotype | Patient | Age/Sex | Clinical status | 1762-1764 | 1858 | 1896 | CPMs | UPMs |
A | A1 | 55/M | Cirrhosis | AGG | C | G | 0 | 0 |
A2 | 41/F | Cirrhosis | AGG | C | G | 0 | 0 | |
A3 | 45/M | Cirrhosis, HCC | AGG | C | G | 0 | 1 | |
A4 | 40/F | Cirrhosis | AGG | C | G | 0 | 0 | |
A5 | 10/F | Asymptomatic | TGA (mutant) | C | G | 1 | 6 | |
A6 | 52/M | CAH | TGA (mutant) | C | G | 1 | 8 | |
A7 | 38/M | CAH | AGG | C | G | 0 | 2 | |
A8 | 54/M | Cirrhosis | AGG | C | G | 0 | 0 | |
A9 | 52/M | CAH | AGG | C | G | 0 | 4 | |
A10 | 39/M | Asymptomatic | AGG | C | G | 0 | 0 | |
D | D1 | 36/M | CAH | AGG | T | G | 0 | 2 |
D2 | 54/F | Asymptomatic | TGA (mutant) | T | A (stop) | 2 | 7 | |
D3 | 56/F | CAH | TGA (mutant) | T | A (stop) | 2 | 13 | |
D4 | 35/M | Cirrhosis | TGA (mutant) | T | A (stop) | 2 | 5 | |
D5 | 55/M | CAH | TGA (mutant) | T | A (stop) | 2 | 8 | |
D6 | 47/M | Asymptomatic | AGG | T | G | 0 | 6 | |
D7 | 53/M | Asymptomatic | AGG | T | G | 0 | 6 | |
F | F1 | 10/M | Asymptomatic | AGG | C | G | 0 | 7 |
F2 | 35/M | CAH | AGG | T | A (stop) | 1 | 8 |
aNumber of common (CPMs) and uncommon (UPMs) point mutations (see text) in a 200-bp genome segment, from nt 1720 to nt 1919