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Full registry entry

Patient Id

 UMHA1142

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 12

Affected Codon

 580

Affected nucleotide

 1796

Mutation AA

 D580V

Mutation Nuc

 1796A>T

Original-final codons

 GAT>GTT

Affected domain

 A2

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 SEVERE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 ?

ID

 738

 

   
 

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