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Full registry entry

Patient Id

 UMHA1244

Inhibitors

  

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 15

Affected Codon

 1732

Affected nucleotide

 5252

Mutation AA

 K1732R

Mutation Nuc

 5252A>G

Original-final codons

 AAA>AGA

Affected domain

 A3

Refrence

 -

AA change

 Lys>Arg

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 2

FactorAg(%)

 -

Origin

  

ID

 782

 

   
 

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