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Full registry entry

Patient Id

 UMHA0192

Inhibitors

 FAMILIAR

Mutation Type

 SUSTITUTION

Gen

 FVIII

Mutation effect

 MISSENSE

Region

 EXON

Exon inton number

 13

Affected Codon

 680

Affected nucleotide

 2095

Mutation AA

 M680L

Mutation Nuc

 2095A>T

Original-final codons

 ATG>TTG

Affected domain

 A2

Refrence

 -

AA change

 Met>Leu

Diagnostic lab

 UDTM

Coagulopathy

 HA

Severity

 MODERATE

FactorC(%)

 4

FactorAg(%)

 -

Origin

 FAMILIAR

ID

 247

 

   
 

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