Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
NONSENSE |
Region |
EXON |
Exon inton number |
14 |
Affected Codon |
1502 |
Affected nucleotide |
4561 |
Mutation AA |
Q1502X |
Mutation Nuc |
4561C>T |
Original-final codons |
CAG>TAG |
Affected domain |
B |
Refrence |
- |
AA change |
|
Diagnostic lab |
UDTM |
Coagulopathy |
HB |
Severity |
? |
FactorC(%) |
? |
FactorAg(%) |
- |
Origin |
? |
ID |
733 |
|
|
|
|