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Full registry entry

Patient Id

 UMHA0652

Inhibitors

  

Mutation Type

 DELETION

Gen

 FVIII

Mutation effect

 FRAMESHIFT

Region

 EXON

Exon inton number

 25

Affected Codon

 2242

Affected nucleotide

 6782

Mutation AA

 FRAMESHIFT

Mutation Nuc

 6782delG

Original-final codons

 delG

Affected domain

 C2

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 SEVERE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

  

ID

 392

 

   
 

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