l Site map 

 

Spanish English

Home HA mutations HB mutations Contributions Links

 

Full registry entry

Patient Id

 UMHA0217

Inhibitors

 FAMILIAR

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 NONSENSE

Region

 EXON

Exon inton number

 26

Affected Codon

 2307

Affected nucleotide

 6976

Mutation AA

 R2307X

Mutation Nuc

 6976C>T

Original-final codons

 CGA>TGA

Affected domain

 C2

Refrence

 -

AA change

 Arg>Stop

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 SEVERE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 FAMILIAR

ID

 252

 

   
 

© Hemobase.com 2009