All of V0064
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S0265 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/G |
isolated CHD: ASD |
|
S0266 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/A |
isolated CHD: ASD |
|
S0267 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
A/A |
isolated CHD: ASD |
|
S0277 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/G |
isolated CHD: ASD |
|
S0278 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/A |
isolated CHD: ASD |
|
S0279 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
A/A |
isolated CHD: ASD |
|
S0280 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/G |
isolated CHD: ASD |
|
S0281 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
G/A |
isolated CHD: ASD |
|
S0282 |
missense_variant |
CBS |
NM_000071.2:c.919G>A |
A/A |
isolated CHD: ASD |