Table 2 p.Arg656His Variant Prediction by in silico Tools
From: Heterozygous FMN2 missense variant found in a family case of premature ovarian insufficiency
Software | Score | Prediction |
|---|---|---|
Polyphen-2 | 0.733 | Possibly damaging |
M-CAP | 0.050 | Possibly pathogenic |
CADD | 12.700 | Possibly deleterious |