Clinical Study

Mitochondrial Cytochrome c Oxidase Subunit 1 Sequence Variation in Prostate Cancer

Table 3

Missense mutations’ computation methods and prediction of phenotypic effect.

Nucleotide positionAmino acid *PolyPhennsSNP analyzerPMutPMut reliability

C5911TA3VBenignNeutralNeutral3
G5913AD4NBenignNeutralNeutral4
A5935GN11SProbably damagingDiseasePathological1
G5949AG16X
G5973AA24TBenignNeutralPathological6
A6040GN46SBenignNeutralPathological1
G6081AA60TBenignNeutralPathological7
T6124CM74TProbably damagingDiseasePathological9
G6150AV83IBenignNeutralNeutral5
T6253CM117TBenignNeutralPathological7
G6261AA120TBenignNeutralPathological7
G6267AA122TBenignNeutralPathological5
G6285AV128IBenignDiseaseNeutral2
C6340TT146IBenignDiseasePathological9
G6366AV155IBenignNeutralNeutral4
G6480AV193IBenignNeutralNeutral3
A6663GI254VBenignNeutralNeutral7
A6891GS330GBenignNeutralNeutral6
G6924TA341SBenignNeutralPathological1
G7041AV380IBenignDiseaseNeutral4
T7080CF393LBenignDiseasePathological6
A7083GI395V
A7146GT415ABenignNeutralNeutral3
C7147TT415IV*BenignNeutralPathological6
A7158GI419VBenignNeutralNeutral8
A7299GM466VBenignNeutralPathological4
T7354CM484TBenignNeutralPathological0
A7305CM468LBenignNeutralPathological0
T7389CY496HBenignNeutralNeutral5
G7444AX514K

Mut: the method indicates neutral or pathological and provides a reliability index ranging between 0 (low) and 9 (very reliable).
olyPhen2: this method indicates probably damaging (protein function deemed affected with high confidence), possibly damaging (protein function supposedly affected), benign (most likely lacking any phenotypic effect), and unknown (lack of data do not allow PolyPhen to make prediction).
sSNP analyzer: prediction indicates neutral or disease.