Table 2. SH3PXD2B variants.
Variations | BLOSUM62 matrix score | Located within protein domain | Primary congenital glaucoma n=21 | Axenfeld-Reiger syndrome n=30 | POAG n=127 | Normal control subjects n=89 |
---|---|---|---|---|---|---|
Non-synonymous coding sequence variations | ||||||
Gly245Arg | −2 | SH3 #2 | 0 | 0 | 1 | 0 |
Pro295Gln | −1 | - | 0 | 0 | 2 | 2 |
Arg356Gln | 1 | - | 0 | 0 | 1 | 0 |
Glu396Lys | 1 | SH3 #2 | 1 | 0 | 0 | 0 |
Ala431Thr | 0 | - | 0 | 1 | 0 | 0 |
Gly481Arg | −2 | - | 0 | 0 | 1 | 0 |
Pro571Leu | −3 | - | 0 | 1 | 0 | 0 |
Pro826Leu | −3 | - | 0 | 0 | 0 | 1 |
Ile832Val | 3 | - | 0 | 0 | 1 | 0 |
Gly833Glu | −2 | - | 0 | 0 | 0 | 1 |
Glu834Lys | 1 | - | 0 | 0 | 0 | 1 |
Total | 1 | 2 | 6 | 5 | ||
Synonymous coding sequence variations | ||||||
Ala195Ala | - | - | 0 | 0 | 1 | 0 |
Ser174Ser | - | - | 0 | 0 | 3 | 1 |
Ser35Ser | - | - | 16 | 22 | 90 | 61 |
Asp385Asp | - | - | 1 | 0 | 0 | 1 |
Thr428Thr | - | - | 1 | 0 | 0 | 1 |
Intravening sequence variations | ||||||
IVS3–28 a>g | - | - | 3 | 1 | 9 | 4 |
IVS7–11 c>t | - | - | 8 | 13 | 63 | 59 |
IVS7+50 t>c | - | - | 0 | 0 | 3 | 1 |
IVS10–27 a>g | - | - | 5 | 0 | 6 | 9 |
IVS11–9 t>c | - | - | 1 | 1 | 0 | 0 |
IVS11–8 c>t | - | - | 1 | 1 | 0 | 0 |
IVS11–7 g>t | - | - | 0 | 0 | 2 | 1 |
IVS12–43 c>t | - | - | 0 | 0 | 2 | 3 |