All of V0048
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S0109 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
isolated CHD: NA |
|
S0110 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
isolated CHD: NA |
|
S0111 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
isolated CHD: NA |
|
S0112 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
isolated CHD: NA |
|
S0113 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
isolated CHD: NA |
|
S0114 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
isolated CHD: NA |
|
S0115 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0116 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
isolated CHD: NA |
|
S0117 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
isolated CHD: NA |
|
S0118 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
isolated CHD: NA |
|
S0119 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0126 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0128 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0130 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0132 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0134 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
|
S0136 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A |
isolated CHD: NA |
