Allele/Variant Symbol | Allele Synonyms | Category | Variant | Variant type | Molecular consequence | Has Disease Annotations | Has Phenotype Annotations |
---|---|---|---|---|---|---|---|
NC_051350.1:g.41184681G>A | variant | SNP
| |||||
NC_051350.1:g.41184774C>G | variant | SNP
| |||||
NC_051350.1:g.41184444T>C | variant | SNP
| |||||
NC_051350.1:g.41189087T>C | variant | SNP
| |||||
NC_051350.1:g.41181989T>C | variant | SNP
| |||||
NC_051350.1:g.41179131T>A | variant | SNP
| |||||
NC_051350.1:g.41179015A>G | variant | SNP
| |||||
NC_051350.1:g.41184113A>G | variant | SNP
| |||||
NC_051350.1:g.41193969C>T | variant | SNP
| |||||
NC_051350.1:g.41184116A>G | variant | SNP
|