Factor XI Variant Database

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

c.1191T>C

p.Gly397= (Legacy AA No. 379)

Variant Type:

Point

Domain:

Serine Protease

Codon Change:

T>C

Variant Effect:

Silent

No. of Patients Reported:

Phenotype:

None

Allele Count *:

42597

Allele Number *:

282848

Allele Frequency *:

0.150600

Frequency in a random sample of normal volunteers is 18%, making this variant a polymorphism. Martincic et al 1998, Wiewel-Verschueren et al 2017

Structural analysis cannot be performed on this (Point | Silent) variant.

Factor XI Variant Database

Factor XI Gene (F11)