Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAS13g02130 | Scaffold13 | 18083751 | G | A | downstream_gene_variant | MODIFIER | c.*570C>T| |
S183 S198 |
2 | BAS13g02130 | Scaffold13 | 18083810 | C | T | downstream_gene_variant | MODIFIER | c.*511G>A| |
S174 S216 S241 |
3 | BAS13g02130 | Scaffold13 | 18084295 | G | A | downstream_gene_variant | MODIFIER | c.*26C>T| |
S105 S106 |
4 | BAS13g02130 | Scaffold13 | 18084326 | G | A | synonymous_variant | LOW | c.1801C>T|p.Leu601Leu |
S208 S219 |
5 | BAS13g02130 | Scaffold13 | 18085325 | G | A | missense_variant | MODERATE | c.896C>T|p.Ala299Val |
S47 |
6 | BAS13g02130 | Scaffold13 | 18086210 | C | T | synonymous_variant | LOW | c.213G>A|p.Val71Val |
S282 |
7 | BAS13g02130 | Scaffold13 | 18088323 | G | A | upstream_gene_variant | MODIFIER | c.-1901C>T| |
S228 |
8 | BAS13g02130 | Scaffold13 | 18088379 | C | G | upstream_gene_variant | MODIFIER | c.-1957G>C| |
S195 |
9 | BAS13g02130 | Scaffold13 | 18088404 | G | A | upstream_gene_variant | MODIFIER | c.-1982C>T| |
S42 S97 |
10 | BAS13g02130 | Scaffold13 | 18088489 | C | T | upstream_gene_variant | MODIFIER | c.-2067G>A| |
S282 |
11 | BAS13g02130 | Scaffold13 | 18088494 | G | A | upstream_gene_variant | MODIFIER | c.-2072C>T| |
S255 |
12 | BAS13g02130 | Scaffold13 | 18088953 | A | T | upstream_gene_variant | MODIFIER | c.-2531T>A| |
S38 |