Patient Id |
|
|
Inhibitors |
|
Mutation Type |
SUSTITUTION |
Gen |
FVIII |
Mutation effect |
MISSENSE |
Region |
EXON |
Exon inton number |
13 |
Affected Codon |
684 |
Affected nucleotide |
2108 |
Mutation AA |
N684S |
Mutation Nuc |
2108A>G |
Original-final codons |
AAC>AGC |
Affected domain |
A2 |
Refrence |
- |
AA change |
Asn>Ser |
Diagnostic lab |
UDTM |
Coagulopathy |
HA |
Severity |
MILD |
FactorC(%) |
8 |
FactorAg(%) |
- |
Origin |
|
ID |
238 |
|
|
|
|