All of V0050
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S0138 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
NA: NA |
|
S0139 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
NA: NA |
|
S0140 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
NA: NA |
|
S0141 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
NA: NA |
|
S0142 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
NA: NA |
|
S0143 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
NA: NA |
|
S0144 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
NA: NA |
|
S0145 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
NA: NA |
|
S0146 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
NA: NA |
|
S0147 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/G |
NA: NA |
|
S0148 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
G/A |
NA: NA |
|
S0149 |
missense_variant |
MTHFD1 |
NM_001364837.1:c.1958G>A |
A/A |
NA: NA |