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Full registry entry

Patient Id

 UMHA0810

Inhibitors

  

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 16

Affected Codon

 1790

Affected nucleotide

 5425

Mutation AA

 I1790F

Mutation Nuc

 5425A>T

Original-final codons

 ATT>TTT

Affected domain

 A3

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

  

ID

 444

 

   
 

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