Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
NONSENSE |
Region |
EXON |
Exon inton number |
8 |
Affected Codon |
373 |
Affected nucleotide |
1175 |
Mutation AA |
S373X |
Mutation Nuc |
1175C>G |
Original-final codons |
TCA>TGA |
Affected domain |
- |
Refrence |
- |
AA change |
Ser>STOP |
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
SEVERE |
FactorC(%) |
<1 |
FactorAg(%) |
- |
Origin |
FAMILIAR |
ID |
174 |
|
|
|
|