Search Results: 1 unique variant retrieved.



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

  c.212T>C
p.Phe71Ser (Legacy AA No. 31)
Variant Type: 
Point
Domain: 
Gla domain
Location: 
Exon 2
Variant Effect: 
Missense
Codon Change: 
T>C
No. of Patients Reported: 
9
Phenotype: 
I
Allele Count *: 
1
Allele Number *: 
251428
Allele Frequency *: 
0.000004

References and Comments:

Au et al 2004; Jayandharan et al 2005; Akhavan et al 2007
Variant likely induces conformational change and destabilizes FX protein. Legacy cDNA numbering in Au paper - Leytus et al 1986 (c.237T>C)

Patient Information: Show


Structural Interpretation:

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Factor X Variant Database