Search Results: 1 unique variant retrieved.



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

  c.5408A>G
p.His1803Arg (Legacy AA No. 1775)
Variant Type: 
Point
Domain: 
d5A3
Location: 
Exon 16
Variant Effect: 
Missense
Codon Change: 
5408A>G
No. of Patients Reported: 
4
Phenotype: 
Moderate
Association: 
FV Deficiency
Allele Count *: 
7
Allele Number *: 
250934
Allele Frequency *: 
0.000028

References and Comments:

Cutler et al 2010
NA

Patient Information: Show


Structural Interpretation:

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Factor X Variant Database