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Full registry entry

Patient Id

 UMHA0570

Inhibitors

  

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 NONSENSE

Region

 EXON

Exon inton number

 12

Affected Codon

 583

Affected nucleotide

 1804

Mutation AA

 R583X

Mutation Nuc

 1804C>T

Original-final codons

 CGA>TGA

Affected domain

 A2

Refrence

 -

AA change

  

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 ?

FactorC(%)

 ?

FactorAg(%)

 -

Origin

  

ID

 330

 

   
 

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