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Full registy entry

Patient Id

 UMHB0069

Inhibitors

 FAMILIAR

Mutation Type

 SUSTITUTION

Gen

 FIX

Mutation effect

 NONSENSE

Region

 EXON

Exon inton number

 8

Affected Codon

 363

Affected nucleotide

 31208

Mutation AA

 G363X

Mutation Nuc

 31208G>T

Original-final codons

 GGA>TGA

Affected domain

 -

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HB

Severity

 SEVERE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 FAMILIAR

ID

 344

 

   
 

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