Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19330 | A02 | 10021062 | G | A | upstream_gene_variant | MODIFIER | c.-2363G>A| |
S223 |
2 | BAA02g19330 | A02 | 10022492 | G | A | upstream_gene_variant | MODIFIER | c.-933G>A| |
S153 S213 |
3 | BAA02g19330 | A02 | 10022785 | G | A | upstream_gene_variant | MODIFIER | c.-640G>A| |
S133 |
4 | BAA02g19330 | A02 | 10023042 | G | A | upstream_gene_variant | MODIFIER | c.-383G>A| |
S36 |
5 | BAA02g19330 | A02 | 10023080 | G | A | upstream_gene_variant | MODIFIER | c.-345G>A| |
S187 |
6 | BAA02g19330 | A02 | 10023292 | C | T | upstream_gene_variant | MODIFIER | c.-133C>T| |
S244 |
7 | BAA02g19330 | A02 | 10023553 | C | T | synonymous_variant | LOW | c.129C>T|p.Ser43Ser |
S249 |
8 | BAA02g19330 | A02 | 10023691 | C | T | synonymous_variant | LOW | c.267C>T|p.Ser89Ser |
S158 |
9 | BAA02g19330 | A02 | 10024688 | G | A | missense_variant | MODERATE | c.769G>A|p.Asp257Asn |
S59 |
10 | BAA02g19330 | A02 | 10025949 | G | A | downstream_gene_variant | MODIFIER | c.*1076G>A| |
S161 |
11 | BAA02g19330 | A02 | 10027152 | G | A | downstream_gene_variant | MODIFIER | c.*2279G>A| |
S45 |
12 | BAA02g19330 | A02 | 10027161 | G | A | downstream_gene_variant | MODIFIER | c.*2288G>A| |
S133 |
13 | BAA02g19330 | A02 | 10027204 | C | T | downstream_gene_variant | MODIFIER | c.*2331C>T| |
S166 |
14 | BAA02g19330 | A02 | 10027806 | C | T | downstream_gene_variant | MODIFIER | c.*2933C>T| |
S181 |
15 | BAA02g19330 | A02 | 10027984 | G | A | downstream_gene_variant | MODIFIER | c.*3111G>A| |
S173 |