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Full registy entry

Patient Id

 UMHB0043

Inhibitors

  

Mutation Type

 SUSTITUTION

Gen

 FIX

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 4

Affected Codon

 79

Affected nucleotide

 10488

Mutation AA

 G79V

Mutation Nuc

 10488G>T

Original-final codons

 GGA>GTA

Affected domain

 -

Refrence

 -

AA change

 Gly>Val

Diagnostic lab

 UDTM

Coagulopathy

 HB

Severity

 SEVERE

FactorC(%)

 <1

FactorAg(%)

 -

Origin

  

ID

 45

 

   
 

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