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 |
---|---|---|---|---|---|---|---|
NT_037436.4:g.20207928C>T | variant | SNP
| |||||
NT_037436.4:g.20208308T>C | variant | SNP
| |||||
NT_037436.4:g.20208487G>A | variant | SNP
| |||||
NT_037436.4:g.20208421C>T | variant | SNP
| |||||
NT_037436.4:g.20208609G>A | variant | SNP
| |||||
NT_037436.4:g.20208226G>A | variant | SNP
| |||||
NT_037436.4:g.20208796C>T | variant | SNP
| |||||
NT_037436.4:g.20208241A>C | variant | SNP
| |||||
NT_037436.4:g.20207940C>A | variant | SNP
| |||||
NT_037436.4:g.20208139C>T | variant | SNP
|