Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18150 | A02 | 9145097 | C | T | downstream_gene_variant | MODIFIER | c.*359G>A| |
S209 |
2 | BAA02g18150 | A02 | 9146345 | C | T | intron_variant | MODIFIER | c.952-311G>A| |
S175 |
3 | BAA02g18150 | A02 | 9147273 | C | T | missense_variant | MODERATE | c.491G>A|p.Cys164Tyr |
S299 |
4 | BAA02g18150 | A02 | 9147287 | C | T | synonymous_variant | LOW | c.477G>A|p.Glu159Glu |
S179 |
5 | BAA02g18150 | A02 | 9147418 | C | T | missense_variant | MODERATE | c.346G>A|p.Ala116Thr |
S25 |
6 | BAA02g18150 | A02 | 9147644 | C | T | stop_gained | HIGH | c.120G>A|p.Trp40* |
S194 |
7 | BAA02g18150 | A02 | 9147844 | G | A | upstream_gene_variant | MODIFIER | c.-81C>T| |
S136 |
8 | BAA02g18150 | A02 | 9148797 | G | A | upstream_gene_variant | MODIFIER | c.-1034C>T| |
S139 |
9 | BAA02g18150 | A02 | 9149960 | G | A | upstream_gene_variant | MODIFIER | c.-2197C>T| |
S264 |
10 | BAA02g18150 | A02 | 9150487 | A | G | upstream_gene_variant | MODIFIER | c.-2724T>C| |
S134 |
11 | BAA02g18150 | A02 | 9150966 | C | T | upstream_gene_variant | MODIFIER | c.-3203G>A| |
S77 S82 |
12 | BAA02g18150 | A02 | 9151899 | C | T | upstream_gene_variant | MODIFIER | c.-4136G>A| |
S167 |
13 | BAA02g18150 | A02 | 9152760 | C | T | upstream_gene_variant | MODIFIER | c.-4997G>A| |
S9 |