|
Patient Id |
|
 |
|
Inhibitors |
|
|
Mutation Type |
SUSTITUTION |
|
Gen |
FVIII |
|
Mutation effect |
MISSENSE |
|
Region |
EXON |
|
Exon inton number |
13 |
|
Affected Codon |
668 |
|
Affected nucleotide |
2059 |
|
Mutation AA |
L668F |
|
Mutation Nuc |
2059C>T |
|
Original-final codons |
CTC>TTC |
|
Affected domain |
A2 |
|
Refrence |
- |
|
AA change |
Leu>Phe |
|
Diagnostic lab |
UDTM |
|
Coagulopathy |
HA |
|
Severity |
MILD |
|
FactorC(%) |
6 |
|
FactorAg(%) |
- |
|
Origin |
FAMILIAR |
|
ID |
276 |
|
|
|
|
|
