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Full registry entry

Patient Id

 UMHA1048

Inhibitors

  

Mutation Type

 DELETION

Gen

 FVIII

Mutation effect

 FRAMESHIFT

Region

 EXON

Exon inton number

 22

Affected Codon

 2088

Affected nucleotide

 6320

Mutation AA

 FRAMESHIFT

Mutation Nuc

 6320delG

Original-final codons

 6320delG

Affected domain

 C1

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 SEVERE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

  

ID

 714

 

   
 

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