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Table S5 Frequency of nucleotides present in regions flanking the mutated TGA stop codon (N = 35).

From: A meta-analysis of single base-pair substitutions in translational termination codons ('nonstop' mutations) that cause human inherited disease

Base

-6

-5

-4

-3

-2

-1

1

2

3

4

5

6

A

9

9

4

12

12

9

12

9

8

6

10

6

C

7

8

10

13

10

11

4

12

8

9

8

9

G

12

10

11

7

5

9

13

10

9

9

8

8

T

7

8

10

3

8

6

6

4

10

11

9

12

  1. Position 0 corresponding to the stop codon is not shown. Nucleotide frequencies that are significantly higher/lower (p < 0.01) in comparison to the HGMD control dataset are shown in bold