Table 3.
Genotype frequency of four variations in normal blood samples
| Nucletide locationa | 1366 T > G | 2609A > C | 7126delGTT | 10204insAAA | ||||
|---|---|---|---|---|---|---|---|---|
| Amino acida | C386W | K801Q | 2307delL | M3332IK | ||||
| Coding exon | 10 | 11 | 12 | 27 | ||||
| Genotype frequency | 1366 T homozygosity | 2/21 | 2609A homozygosity | 10/22 | insGTT homozygosity | 9/20 | delAAA homozygosity | 5/23 |
| 1366 G homozygosity | 11/21 | 2609 C homozygosity | 3/22 | delGTT homozygosity | 4/20 | insAAA homozygosity | 11/23 | |
| Heterozygosity | 8/21 | Heterozygosity | 9/22 | Heterozygosity | 7/20 | Heterozygosity | 7/23 | |
aNucleotide and amino acid locations are based on AB043895.5