Search Results: 1 unique variant retrieved.



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

  c.1843G>A
p.Val615Met (Legacy AA No. 597)
Variant Type: 
Point
Domain: 
Serine Protease
Codon Change: 
G>A
Variant Effect: 
Missense
No. of Patients Reported: 
0
Phenotype: 
None
Allele Count *: 
105
Allele Number *: 
282852
Allele Frequency *: 
0.000371

Variant Comments & Reference:

Polymorphism. Wiewel-Verschueren et al 2017

Patient Information: Show


Structural Interpretation:

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Factor XI Variant Database