| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g47020 | A01 | 31277909 | C | T | downstream_gene_variant | MODIFIER | c.*896G>A| |
S294 |
| 2 | BAA01g47020 | A01 | 31279068 | C | T | missense_variant | MODERATE | c.677G>A|p.Gly226Glu |
S247 |
| 3 | BAA01g47020 | A01 | 31279283 | C | T | missense_variant | MODERATE | c.462G>A|p.Met154Ile |
S216 |
| 4 | BAA01g47020 | A01 | 31279436 | C | T | synonymous_variant | LOW | c.309G>A|p.Glu103Glu |
S126 |
| 5 | BAA01g47020 | A01 | 31280107 | C | T | upstream_gene_variant | MODIFIER | c.-222G>A| |
S28 |
| 6 | BAA01g47020 | A01 | 31280614 | C | T | upstream_gene_variant | MODIFIER | c.-729G>A| |
S210 S225 |
| 7 | BAA01g47020 | A01 | 31280782 | G | A | upstream_gene_variant | MODIFIER | c.-897C>T| |
S268 |
| 8 | BAA01g47020 | A01 | 31280911 | C | T | upstream_gene_variant | MODIFIER | c.-1026G>A| |
S58 |
| 9 | BAA01g47020 | A01 | 31280984 | G | A | upstream_gene_variant | MODIFIER | c.-1099C>T| |
S34 |
| 10 | BAA01g47020 | A01 | 31280999 | T | A | upstream_gene_variant | MODIFIER | c.-1114A>T| |
S217 S261 S308 |
| 11 | BAA01g47020 | A01 | 31281285 | G | A | upstream_gene_variant | MODIFIER | c.-1400C>T| |
S70 |
| 12 | BAA01g47020 | A01 | 31282224 | C | T | upstream_gene_variant | MODIFIER | c.-2339G>A| |
S28 |
| 13 | BAA01g47020 | A01 | 31282351 | G | A | upstream_gene_variant | MODIFIER | c.-2466C>T| |
S144 |
| 14 | BAA01g47020 | A01 | 31283105 | C | T | upstream_gene_variant | MODIFIER | c.-3220G>A| |
S42 |
| 15 | BAA01g47020 | A01 | 31283292 | G | A | upstream_gene_variant | MODIFIER | c.-3407C>T| |
S298 |
| 16 | BAA01g47020 | A01 | 31283724 | G | A | upstream_gene_variant | MODIFIER | c.-3839C>T| |
S115 |
| 17 | BAA01g47020 | A01 | 31283728 | G | A | upstream_gene_variant | MODIFIER | c.-3843C>T| |
S226 |
| 18 | BAA01g47020 | A01 | 31284369 | C | T | upstream_gene_variant | MODIFIER | c.-4484G>A| |
S174 |