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Full registy entry

Patient Id

 UMHB0216

Inhibitors

 ?

Mutation Type

 DELETION

Gen

 FIX

Mutation effect

  

Region

 EXON

Exon inton number

 4

Affected Codon

 76-77

Affected nucleotide

 10479-10484

Mutation AA

 Gly76_Phe77del

Mutation Nuc

 10479-10484del

Original-final codons

 10479-10484delGATTTG

Affected domain

 -

Refrence

 -

AA change

 Gly76_Phe77del

Diagnostic lab

 UDTM

Coagulopathy

 HB

Severity

 ?

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 ?

ID

 806

 

   
 

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