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Full registy entry

Patient Id

 UMHB0128

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FIX

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 5

Affected Codon

 114

Affected nucleotide

 17755

Mutation AA

 G114R

Mutation Nuc

 17755G>A

Original-final codons

 GGA>AGA

Affected domain

 -

Refrence

 -

AA change

 Gly>Arg

Diagnostic lab

 UDTM

Coagulopathy

 HB

Severity

 ?

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 ?

ID

 798

 

   
 

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