Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11040 | A02 | 4983232 | G | A | downstream_gene_variant | MODIFIER | c.*1205C>T| |
S87 |
2 | BAA02g11040 | A02 | 4983639 | A | T | downstream_gene_variant | MODIFIER | c.*798T>A| |
S68 |
3 | BAA02g11040 | A02 | 4985474 | G | A | missense_variant | MODERATE | c.626C>T|p.Ala209Val |
S288 |
4 | BAA02g11040 | A02 | 4986269 | G | A | missense_variant | MODERATE | c.253C>T|p.Pro85Ser |
S168 |
5 | BAA02g11040 | A02 | 4987375 | G | A | upstream_gene_variant | MODIFIER | c.-854C>T| |
S50 |
6 | BAA02g11040 | A02 | 4988786 | G | A | upstream_gene_variant | MODIFIER | c.-2265C>T| |
S57 |
7 | BAA02g11040 | A02 | 4990419 | C | T | upstream_gene_variant | MODIFIER | c.-3898G>A| |
S18 |
8 | BAA02g11040 | A02 | 4990485 | G | A | upstream_gene_variant | MODIFIER | c.-3964C>T| |
S5 |
9 | BAA02g11040 | A02 | 4991265 | C | T | upstream_gene_variant | MODIFIER | c.-4744G>A| |
S273 |
10 | BAA02g11040 | A02 | 4991325 | C | T | upstream_gene_variant | MODIFIER | c.-4804G>A| |
S209 |
11 | BAA02g11040 | A02 | 4991460 | C | T | upstream_gene_variant | MODIFIER | c.-4939G>A| |
S241 |
12 | BAA02g11040 | A02 | 4991493 | G | A | upstream_gene_variant | MODIFIER | c.-4972C>T| |
S166 |