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. 2017 Dec 18;6:e27469. doi: 10.7554/eLife.27469

Table 4. Estimation of the fraction of non-synonymous SNVs that lead to a phenotype.

Table 4—source data 1. Estimation of the fraction of SNVs and Indels that leads to a phenotype.
DOI: 10.7554/eLife.27469.011
Table 4—source data 2. Estimated mutation rates.
DOI: 10.7554/eLife.27469.012
ura4 ura5 Total
(265 Aa) (216 Aa) (481 Aa)
Potential SNVs Synonymous 530 (0.22) 443 (0.23) 973 (0.22)
Non-synonymous 1739 (0.73) 1405 (0.72) 3144 (0.73)
STOPs 116 (0.05) 96 (0.05) 212 (0.05)
Observed SNVs Synonymous 3 (0.03) 2 (0.03) 5 (0.03)
Non-synonymous 74 (0.69) 58 (0.73) 132 (0.71)
STOPs 29 (0.27) 19 (0.24) 48 (0.26)
Non-coding 1 (0.01) 0 (0.00) 1 (0.00)
Different mutations per Aa (41,13,3) (23,7,5,0,0,1) (64,20,8,0,0,1)
Independent identical mutations per non-syn SNV (64,9,1) (41,11,2,1,1,0,1, 0,1) (105,20,3,1,1,0,1, 0,1)
Method 1 Essential Aa (ML) 124 54 170
(Essential Aa) [CI 95%] [93,202] [43,81] [140,228]
f 0.47 0.25 0.35
[CI 95%] [0.35,0.76] [0.20,0.38] [0.29,0.47]
Method 2 Essential NS (ML) 296 88 276
(Non-Syn) [CI 95%] [195,394] [73,118] [228,362]
f 0.17 0.06 0.09
[CI 95%] [0.11,0.23] [0.05,0.08] [0.07,0.12]
Method 3 # STOPs among all potentials STOPs 0.25 0.20 0.23
(LM08) f 0.17 0.21 0.19