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Full registry entry

Patient Id

 UMHA0294

Inhibitors

 ?

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 NONSENSE

Region

 EXON

Exon inton number

 8

Affected Codon

 382

Affected nucleotide

 1202

Mutation AA

 W382X

Mutation Nuc

 1202G>A

Original-final codons

 TGG>TAG

Affected domain

 A2

Refrence

 -

AA change

 Trp>Stop

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 SEVERE

FactorC(%)

 1

FactorAg(%)

 -

Origin

 ?

ID

 267

 

   
 

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