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Figure 3 | BMC Genetics

Figure 3

From: The rhesus macaque is three times as diverse but more closely equivalent in damaging coding variation as compared to the human

Figure 3

Analysis of homozygosity/heterozygosity for cSNPs, based on the idea that severely damaging variants are less likely to be homozygous. H.S: human synonymous cSNPs; M.S: macaque synonymous cSNPs; H.B: human nsSNPs predicted to be “benign” by PolyPhen; M.B: macaque nsSNPs predicted to be “benign” by PolyPhen; H.D: human nsSNPs predicted to be damaging by PolyPhen; M.D: macaque nsSNPs predicted to be damaging by PolyPhen.

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