Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
NONSENSE |
Region |
EXON |
Exon inton number |
26 |
Affected Codon |
2307 |
Affected nucleotide |
6976 |
Mutation AA |
R2307X |
Mutation Nuc |
6976C>T |
Original-final codons |
CGA>TGA |
Affected domain |
C2 |
Refrence |
- |
AA change |
Arg>Stop |
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
SEVERE |
FactorC(%) |
? |
FactorAg(%) |
- |
Origin |
FAMILIAR |
ID |
252 |
|
|
|
|