Search Results: 1 unique variant retrieved.



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

  c.1324G>A
p.Gly442Ser (Legacy AA No. 402)
Variant Type: 
Point
Domain: 
Serine protease
Location: 
Exon 8
Variant Effect: 
Missense
Codon Change: 
G>A
No. of Patients Reported: 
0
Phenotype: 
U
Allele Count *: 
-
Allele Number *: 
-
Allele Frequency *: 
-

References and Comments:

Perry 1997
Legacy cDNA numbering in paper - Leytus et al 1986 (c.1349G>A)

Patient Information: Show


Structural Interpretation:

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Factor X Variant Database