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Full registry entry

Patient Id

 UMHA0036

Inhibitors

 ?

Mutation Type

 INVERSION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 13

Affected Codon

 674

Affected nucleotide

 2077-2078

Mutation AA

 S674L

Mutation Nuc

 2077_2078inv

Original-final codons

 TCA>CTA

Affected domain

 A2

Refrence

 -

AA change

 Ser>Leu

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 ?

FactorAg(%)

 -

Origin

 ?

ID

 216

 

   
 

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