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 |
---|---|---|---|---|---|---|---|
NC_003281.10:g.486313C>T | variant | SNP
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NC_003281.10:g.486379T>G | variant | SNP
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NC_003281.10:g.486250C>T | variant | SNP
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NC_003281.10:g.486509C>T | variant | SNP
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NC_003281.10:g.486312C>T | variant | SNP
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NC_003281.10:g.486517A>T | variant | SNP
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NC_003281.10:g.486261C>T | variant | SNP
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NC_003281.10:g.486515G>A | variant | SNP
| |||||
NC_003281.10:g.486218C>T | variant | SNP
|