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Full registry entry

Patient Id

 UMHA0596

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 NONSENSE

Region

 EXON

Exon inton number

 1

Affected Codon

 -5

Affected nucleotide

 43

Mutation AA

 R-5X

Mutation Nuc

 43C>T

Original-final codons

 CGA>TGA

Affected domain

 PÉPTIDO SEÑAL

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 1,5-2

FactorAg(%)

 -

Origin

 ?

ID

 346

 

   
 

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