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Full registry entry

Patient Id

 UMHA0990

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 26

Affected Codon

 2322

Affected nucleotide

 7022

Mutation AA

 E2322G

Mutation Nuc

 7022A>G

Original-final codons

 GAG>GGG

Affected domain

 C2

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 2-3

FactorAg(%)

 -

Origin

 ?

ID

 694

 

   
 

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