Table 1 Polymorphisms in the hydroxynitrile glucoside biosynthesis genes and resulting amino acid substitutions.

CYP79A12

P, M

1–168

1–56 (several; more similarity to Bowman)

P, M

220A → G

N74D

P, M

510T → G

I170M

P, M

712A → G

I238V

M

1010C → A

P337Q

CYP79A8

E, M

473C → G

A158G

E, M

996G → C

K332N

E, M

1016G → A

R339Q

CYP71L1

P, M

127A → G

N43D

CYP71U5

E, M

419A → C

Q1450P

E, P, M

833T → C

V278A

P

896A → G

N299S

E, M

1060G → A

V354I

E, M

1264G → A

G422S

E, M

1402C → A

H468N

E, M

1426G → A

E476T

E, M

1427A → C

E476T

E, M

1441C → G

Q481E

CYP71C103

M

554G → C

S185T

M

1059C → A

D353E

P

1163T → C

I388T

M

1235G → C

S412T

M

1448A → C

E483A

CYP71C113

P

23A → G

E8G

M

74T → C

M25T

P

88G → A

G30R

M

121C → T

R41C

P

1168G → A

V390I

UGT85F22

P, M

315G → C

Q105H

M

608C → T

T203I

P, M

679A → G

I227V

P, M

748C → A

P250T

P

1334A → G

E445G

M

1345G → A

G449R

P

1397C → G

A466G

M

1435G → A

V479I

UGT85F23

P, M

1489C → T

P497S