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Table S6 Frequency of nucleotides occurring within regions flanking mutated stop codons harbouring single nonstop mutations.

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

21

19

11

21

21

14

26

15

16

11

23

16

C

14

17

19

19

19

19

11

19

22

21

18

23

G

19

18

22

9

5

17

21

23

13

14

14

14

T

14

14

16

19

23

18

10

11

17

22

13

15

  1. Position 0 corresponding to the stop codon is not shown. Frequencies which are significantly higher/lower (p < 0.01) in comparison with corresponding HGMD controls are shown underlined