All of V0426
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S1073 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: VSD |
|
S1074 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: PDA |
|
S1075 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: ASD |
|
S1076 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: AVSD |
|
S1077 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: TGA |
|
S1078 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: TOF |
|
S1079 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: PTA |
|
S1080 |
5_prime_UTR_variant |
TFAP2B |
NM_003221.4:c.-34G>A |
A |
isolated CHD: DORV |
