Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g00080 | Scaffold13 | 4241803 | C | T | downstream_gene_variant | MODIFIER | c.*1476G>A| |
S47 |
2 | BAS13g00080 | Scaffold13 | 4243389 | G | A | missense_variant | MODERATE | c.1201C>T|p.His401Tyr |
S153 |
3 | BAS13g00080 | Scaffold13 | 4243617 | G | A | missense_variant | MODERATE | c.973C>T|p.Pro325Ser |
S216 |
4 | BAS13g00080 | Scaffold13 | 4244744 | G | A | missense_variant | MODERATE | c.511C>T|p.Pro171Ser |
S292 |
5 | BAS13g00080 | Scaffold13 | 4245414 | G | A | missense_variant | MODERATE | c.235C>T|p.Leu79Phe |
S125 |
6 | BAS13g00080 | Scaffold13 | 4245447 | C | T | missense_variant | MODERATE | c.202G>A|p.Glu68Lys |
S135 |
7 | BAS13g00080 | Scaffold13 | 4246859 | G | A | upstream_gene_variant | MODIFIER | c.-1211C>T| |
S263 |