Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16150 | A02 | 7866981 | G | A | upstream_gene_variant | MODIFIER | c.-2195G>A| |
S136 |
2 | BAA02g16150 | A02 | 7867053 | G | A | upstream_gene_variant | MODIFIER | c.-2123G>A| |
S217 S248 |
3 | BAA02g16150 | A02 | 7867274 | G | A | upstream_gene_variant | MODIFIER | c.-1902G>A| |
S203 |
4 | BAA02g16150 | A02 | 7868450 | G | A | upstream_gene_variant | MODIFIER | c.-726G>A| |
S161 |
5 | BAA02g16150 | A02 | 7869072 | C | T | upstream_gene_variant | MODIFIER | c.-104C>T| |
S55 |
6 | BAA02g16150 | A02 | 7869416 | C | T | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S32 |
7 | BAA02g16150 | A02 | 7870939 | G | A | synonymous_variant | LOW | c.1764G>A|p.Lys588Lys |
S87 |
8 | BAA02g16150 | A02 | 7871634 | C | T | downstream_gene_variant | MODIFIER | c.*689C>T| |
S131 |
9 | BAA02g16150 | A02 | 7871909 | C | T | downstream_gene_variant | MODIFIER | c.*964C>T| |
S206 S26 |
10 | BAA02g16150 | A02 | 7872272 | G | A | downstream_gene_variant | MODIFIER | c.*1327G>A| |
S296 |
11 | BAA02g16150 | A02 | 7872685 | C | T | downstream_gene_variant | MODIFIER | c.*1740C>T| |
S208 |
12 | BAA02g16150 | A02 | 7873543 | C | T | downstream_gene_variant | MODIFIER | c.*2598C>T| |
S13 |
13 | BAA02g16150 | A02 | 7874632 | C | T | downstream_gene_variant | MODIFIER | c.*3687C>T| |
S71 |
14 | BAA02g16150 | A02 | 7874683 | C | T | downstream_gene_variant | MODIFIER | c.*3738C>T| |
S211 S227 |