Gene symbol | Rank | Alignment Length (aa) | Similarity % | Identity % | Method Count | Method Ensembl ComparaHGNCInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidSGD |
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Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
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NC_000078.7:g.90781974A>G | variant | SNP
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NC_000078.7:g.90782023A>G | variant | SNP
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NC_000078.7:g.90781990T>C | variant | SNP
|