|
Patient Id |
|
 |
|
Inhibitors |
|
|
Mutation Type |
DELETION |
|
Gen |
FVIII |
|
Mutation effect |
AMINOACID DELETION |
|
Region |
EXON |
|
Exon inton number |
13 |
|
Affected Codon |
653 |
|
Affected nucleotide |
2015-2017 |
|
Mutation AA |
F653del |
|
Mutation Nuc |
2015-2017delTCT |
|
Original-final codons |
delTCT |
|
Affected domain |
A2 |
|
Refrence |
- |
|
AA change |
Phe653del |
|
Diagnostic lab |
UDTM |
|
Coagulopathy |
HA |
|
Severity |
SEVERE |
|
FactorC(%) |
? |
|
FactorAg(%) |
- |
|
Origin |
? |
|
ID |
781 |
|
|
|
|
|
