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Table 4 Translational effect of single-nucleotide polymorphisms (SNPs) located in the genes from “common 21 pool”

From: Identification of quantitative trait loci associated with leaf rust resistance in rye by precision mapping

SNP-DArT markera

Consequence

Impact

cDNA position

CDS position

Protein position

Amino acids

Codons

Strand

7467766|F|0–6:T > G

missense variant

mod

59

59

20

Y/S

tAc/tCc

-1

3730018|F|0–57:A > G

intron variant

mof

-

-

-

-

-

1

3362858|F|0–20:G > C

synonymous variant

low

522

522

174

G

ggC/ggG

-1

5203314|F|0–14:C > T

synonymous variant

low

390

390

130

A

gcC/gcT

1

3603211|F|0–20:C > G

missense variant

mod

384

384

128

E/D

gaG/gaC

-1

3597912|F|0–20:C > T

missense variant

mod

856

856

286

V/M

Gtg/Atg

-1

3596033|F|0–14:T > C

synonymous variant

low

2232

2232

744

T

acA/acG

-1

3596652|F|0–30:A > G

synonymous variant

low

1017

1017

339

S

tcT/tcC

-1

3591362|F|0–11:A > C

synonymous variant

low

420

420

140

A

gcT/gcG

-1

3345552|F|0–36:A > G

missense variant

mod

701

701

234

M/T

aTg/aCg

-1

5034809|F|0–32:G > C

missense variant

mod

177

177

59

E/D

gaG/gaC

1

3594357|F|0–29:A > C

stop lost

high

553

553

185

*/E

Tag/Gag

-1

3587847|F|0–44:C > A

missense variant

mod

681

681

227

E/D

gaG/gaT

-1

3349900|F|0–20:T > C

synonymous variant

low

1551

1551

517

N

aaT/aaC

1

3344187|F|0–12:G > C

missense variant

mod

1580

1580

527

S/T

aGc/aCc

1

3899895|F|0–56:G > A

intron variant

mof

-

-

-

-

-

1

75511600|F|0–32:T > G

synonymous variant

low

495

495

165

A

gcT/gcG

1

5503350|F|0–5:G > A

synonymous variant

low

228

228

76

H

caC/caT

-1

3353307|F|0–11:T > C

synonymous variant

low

2286

2286

762

L

ctT/ctC

1

3360254|F|0–23:C > T

intron variant

mof

-

-

-

-

-

-1

3596868|F|0–24:T > C

synonymous variant

low

1368

1368

456

V

gtA/gtG

-1

  1. aFirst, reference allele; second, alternative allele. mod, referred to moderate impact; mof referred to modifier impact; L referred to low impact. Marker location and gene ID are given in Table 3