Species | Gene symbol | Count | Best | Best reverse | Method Ensembl ComparaHGNCHieranoidInParanoidOMAOrthoFinderOrthoInspectorPANTHERPhylomeDBSonicParanoidXenbaseZFIN |
---|---|---|---|---|---|
Homo sapiens | CEP128 | 1 of 10 | Yes | Yes | ☐☑☐☐☐☐☐☐☐☐ |
Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
---|---|---|---|---|---|---|---|
NC_051341.1:g.109951013G>T | variant | SNP
| |||||
NC_051341.1:g.110196340G>A | variant | SNP
| |||||
variant | SNP
| ||||||
NC_051341.1:g.110148446T>C | variant | SNP
| |||||
NC_051341.1:g.110161055C>T | variant | SNP
| |||||
NC_051341.1:g.110164665A>C | variant | SNP
| |||||
NC_051341.1:g.110189891A>G | variant | SNP
| |||||
NC_051341.1:g.110191063G>A | variant | SNP
| |||||
NC_051341.1:g.110191386G>A | variant | SNP
| |||||
NC_051341.1:g.110191624C>T | variant | SNP
|