Search Results: 1 unique variant retrieved.
Terms with a '*' next to them are explained on the Help Page .
c.5842T>C
p.Trp1948Arg (Legacy AA No. 1920)
Variant Type:
Point
Domain:
d5C1
Location:
Exon 20
Variant Effect:
Missense
Codon Change:
5842T>C
No. of Patients Reported:
3
Phenotype:
Mild
Association:
thrombosis
Allele Count *:
NA
Allele Number *:
NA
Allele Frequency *:
NA
References and Comments:
Nogami et al 2014DVT with swelling of lower body; more APC resistance compared to FV Leiden