| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 218051 | BAA02g32770 | A02 | 28032837 | G | T | downstream_gene_variant | MODIFIER | c.*1128G>T| |
S165 S211 S227 S255 |
| 218052 | BAA02g32770 | A02 | 28032918 | G | A | downstream_gene_variant | MODIFIER | c.*1209G>A| |
S127 |
| 218053 | BAA02g32770 | A02 | 28033075 | C | T | downstream_gene_variant | MODIFIER | c.*1366C>T| |
S206 |
| 218054 | BAA02g32770 | A02 | 28033252 | G | A | downstream_gene_variant | MODIFIER | c.*1543G>A| |
S110 S50 |
| 218055 | BAA02g32770 | A02 | 28033422 | G | A | downstream_gene_variant | MODIFIER | c.*1713G>A| |
S228 |
| 218056 | BAA02g32770 | A02 | 28033518 | C | T | downstream_gene_variant | MODIFIER | c.*1809C>T| |
S202 |
| 218057 | BAA02g32770 | A02 | 28033982 | C | T | downstream_gene_variant | MODIFIER | c.*2273C>T| |
S92 |
| 218058 | BAA02g32780 | A02 | 28035722 | G | A | upstream_gene_variant | MODIFIER | c.-4129G>A| |
S190 |
| 218059 | BAA02g32780 | A02 | 28036775 | C | T | upstream_gene_variant | MODIFIER | c.-3076C>T| |
S208 |
| 218060 | BAA02g32780 | A02 | 28037221 | C | T | upstream_gene_variant | MODIFIER | c.-2630C>T| |
S53 |
| 218061 | BAA02g32780 | A02 | 28037523 | G | A | upstream_gene_variant | MODIFIER | c.-2328G>A| |
S84 S93 |
| 218062 | BAA02g32780 | A02 | 28037596 | C | T | upstream_gene_variant | MODIFIER | c.-2255C>T| |
S289 S290 |
| 218063 | BAA02g32780 | A02 | 28038148 | C | T | upstream_gene_variant | MODIFIER | c.-1703C>T| |
S173 |
| 218064 | BAA02g32780 | A02 | 28039672 | C | T | upstream_gene_variant | MODIFIER | c.-179C>T| |
S120 |
| 218065 | BAA02g32780 | A02 | 28039970 | C | T | intron_variant | MODIFIER | c.97+23C>T| |
S138 |
| 218066 | BAA02g32780 | A02 | 28043822 | G | A | intron_variant | MODIFIER | c.1136+1241G>A| |
S267 |
| 218067 | BAA02g32780 | A02 | 28044450 | G | A | intron_variant | MODIFIER | c.1136+1869G>A| |
S188 |
| 218068 | BAA02g32780 | A02 | 28047059 | A | T | intron_variant | MODIFIER | c.1137-3706A>T| |
S116 |
| 218069 | BAA02g32780 | A02 | 28047258 | C | T | intron_variant | MODIFIER | c.1137-3507C>T| |
S130 |
| 218070 | BAA02g32780 | A02 | 28047735 | G | A | intron_variant | MODIFIER | c.1137-3030G>A| |
S306 S308 |
| 218071 | BAA02g32780 | A02 | 28048929 | C | T | intron_variant | MODIFIER | c.1137-1836C>T| |
S162 |
| 218072 | BAA02g32780 | A02 | 28048936 | G | A | intron_variant | MODIFIER | c.1137-1829G>A| |
S187 |
| 218073 | BAA02g32780 | A02 | 28049099 | C | T | intron_variant | MODIFIER | c.1137-1666C>T| |
S122 |
| 218074 | BAA02g32780 | A02 | 28051056 | G | A | intron_variant | MODIFIER | c.1244-28G>A| |
S126 |
| 218075 | BAA02g32780 | A02 | 28051100 | C | T | synonymous_variant | LOW | c.1260C>T|p.Ile420Ile |
S246 |