Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
MISSENSE |
Region |
EXON |
Exon inton number |
18 |
Affected Codon |
1960 |
Affected nucleotide |
5936 |
Mutation AA |
G1960E |
Mutation Nuc |
5936G>A |
Original-final codons |
GGA>GAA |
Affected domain |
A3 |
Refrence |
- |
AA change |
|
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
MILD |
FactorC(%) |
14 |
FactorAg(%) |
- |
Origin |
FAMILIAR |
ID |
354 |
|
|
|
|