All of V0573
| ID |
Consequence |
Gene/Location |
Detail |
Geno Type |
CHD Type |
|
S1335 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/TC+CC(recessive) |
isolated CHD: NA |
|
S1336 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(genotypic) |
isolated CHD: NA |
|
S1337 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
T/C(multiplicative) |
isolated CHD: NA |
|
S1338 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(additive) |
isolated CHD: NA |
|
S1339 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT+TC/CC(dominant) |
isolated CHD: NA |
|
S1340 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/TC+CC(recessive) |
isolated CHD: NA |
|
S1341 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(genotypic) |
isolated CHD: NA |
|
S1342 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
T/C(multiplicative) |
isolated CHD: NA |
|
S1343 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(additive) |
isolated CHD: NA |
|
S1344 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT+TC/CC(dominant) |
isolated CHD: NA |
|
S1345 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/TC+CC(recessive) |
isolated CHD: NA |
|
S1346 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(genotypic) |
isolated CHD: NA |
|
S1347 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
T/C(multiplicative) |
isolated CHD: NA |
|
S1348 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(additive) |
isolated CHD: NA |
|
S1349 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT+TC/CC(dominant) |
isolated CHD: NA |
|
S1350 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/TC+CC(recessive) |
isolated CHD: NA |
|
S1351 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(genotypic) |
isolated CHD: NA |
|
S1352 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
T/C(multiplicative) |
isolated CHD: NA |
|
S1353 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT/CT/CC(additive) |
isolated CHD: NA |
|
S1354 |
synonymous_variant |
SMAD7 |
NM_005904.3:c.894C>T |
TT+TC/CC(dominant) |
isolated CHD: NA |
