|
Patient Id |
|
 |
|
Inhibitors |
|
|
Mutation Type |
SUSTITUTION |
|
Gen |
FVIII |
|
Mutation effect |
MISSENSE |
|
Region |
EXON |
|
Exon inton number |
16 |
|
Affected Codon |
1836 |
|
Affected nucleotide |
5564 |
|
Mutation AA |
A1836D |
|
Mutation Nuc |
5564C>A |
|
Original-final codons |
GCT>GAT |
|
Affected domain |
A3 |
|
Refrence |
- |
|
AA change |
Ala>Asp |
|
Diagnostic lab |
UDTM |
|
Coagulopathy |
HA |
|
Severity |
MODERATE |
|
FactorC(%) |
? |
|
FactorAg(%) |
- |
|
Origin |
? |
|
ID |
164 |
|
|
|
|
|
