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Fig. 4 | BMC Genomics

Fig. 4

From: mGAP: the macaque genotype and phenotype resource, a framework for accessing and interpreting macaque variant data, and identifying new models of human disease

Fig. 4

The mGAP genome browser. Variants of interest may be searched by chromosome position or gene name in the search bar. Diamonds indicate SNVs and bars indicate indels, with colors indicating predicted impact on protein coding (red = high, yellow = moderate, blue = low). Clicking a variant provides a detailed pop-up with summary and annotations. The provided information includes predicted function, regulatory data, species conservation, phenotypic data, allele frequencies, and genotypes by animal

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