Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
MISSENSE |
Region |
EXON |
Exon inton number |
24 |
Affected Codon |
2209 |
Affected nucleotide |
6683 |
Mutation AA |
R2209Q |
Mutation Nuc |
6683G>A |
Original-final codons |
CGA>CAA |
Affected domain |
C2 |
Refrence |
- |
AA change |
|
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
MILD |
FactorC(%) |
? |
FactorAg(%) |
- |
Origin |
|
ID |
372 |
|
|
|
|