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Full registry entry

Patient Id

 UMHA0318

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 14

Affected Codon

 1689

Affected nucleotide

 5123

Mutation AA

 R1689H

Mutation Nuc

 5123G>A

Original-final codons

 CGC>CAC

Affected domain

 -

Refrence

 -

AA change

 Arg>His

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MILD

FactorC(%)

 26

FactorAg(%)

 -

Origin

 ?

ID

 296

 

   
 

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