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Full registy entry

Patient Id

 UMHB0045

Inhibitors

  

Mutation Type

 SUSTITUTION

Gen

 FIX

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 8

Affected Codon

 390

Affected nucleotide

 31289

Mutation AA

 A390S

Mutation Nuc

 31289G>T

Original-final codons

 GCA>TCA

Affected domain

 -

Refrence

 -

AA change

 Ala>Ser

Diagnostic lab

 UDTM

Coagulopathy

 HB

Severity

 MODERATE

FactorC(%)

 5

FactorAg(%)

 -

Origin

  

ID

 47

 

   
 

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