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Full registry entry

Patient Id

 UMHA1254

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 11

Affected Codon

 550

Affected nucleotide

 1706

Mutation AA

 P550R

Mutation Nuc

 1706C>G

Original-final codons

 CCT>CGT

Affected domain

 A2

Refrence

 -

AA change

 Pro>Arg

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 ?

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 ?

ID

 786

 

   
 

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