Search Results: 1 unique variant retrieved.



Terms with a '*' next to them are explained on the Help Page .

  c.19C>A
p.Leu7Ile (Legacy AA No. -34)
Variant Type: 
Point
Domain: 
Pre-pro leader
Location: 
Exon 1
Variant Effect: 
Missense
Codon Change: 
C>A
No. of Patients Reported: 
0
Phenotype: 
U
Allele Count *: 
7
Allele Number *: 
279678
Allele Frequency *: 
0.000025

References and Comments:

Camire et al 2001; Uprichard & Perry 2002

Patient Information: Show


Structural Interpretation:

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Factor X Variant Database