|
Patient Id |
|
 |
|
Inhibitors |
|
|
Mutation Type |
SUSTITUTION |
|
Gen |
FVIII |
|
Mutation effect |
MISSENSE |
|
Region |
EXON |
|
Exon inton number |
11 |
|
Affected Codon |
550 |
|
Affected nucleotide |
1706 |
|
Mutation AA |
P550R |
|
Mutation Nuc |
1706C>G |
|
Original-final codons |
CCT>CGT |
|
Affected domain |
A2 |
|
Refrence |
- |
|
AA change |
Pro>Arg |
|
Diagnostic lab |
UDTM |
|
Coagulopathy |
HA |
|
Severity |
? |
|
FactorC(%) |
? |
|
FactorAg(%) |
- |
|
Origin |
? |
|
ID |
786 |
|
|
|
|
|
