Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
NONSENSE |
Region |
EXON |
Exon inton number |
8 |
Affected Codon |
382 |
Affected nucleotide |
1202 |
Mutation AA |
W382X |
Mutation Nuc |
1202G>A |
Original-final codons |
TGG>TAG |
Affected domain |
A2 |
Refrence |
- |
AA change |
Trp>Stop |
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
SEVERE |
FactorC(%) |
1 |
FactorAg(%) |
- |
Origin |
? |
ID |
267 |
|
|
|
|