| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 154051 | BAA02g02400 | A02 | 1072473 | G | A | upstream_gene_variant | MODIFIER | c.-4705C>T| |
S238 |
| 154052 | BAA02g02420 | A02 | 1074218 | G | A | downstream_gene_variant | MODIFIER | c.*2088G>A| |
S265 |
| 154053 | BAA02g02420 | A02 | 1075554 | G | A | downstream_gene_variant | MODIFIER | c.*3424G>A| |
S197 |
| 154054 | BAA02g02440 | A02 | 1081350 | G | A | upstream_gene_variant | MODIFIER | c.-783C>T| |
S176 |
| 154055 | BAA02g02440 | A02 | 1082789 | C | T | upstream_gene_variant | MODIFIER | c.-2222G>A| |
S298 |
| 154056 | BAA02g02440 | A02 | 1082932 | G | A | upstream_gene_variant | MODIFIER | c.-2365C>T| |
S165 |
| 154057 | BAA02g02440 | A02 | 1083476 | G | A | upstream_gene_variant | MODIFIER | c.-2909C>T| |
S189 |
| 154058 | BAA02g02450 | A02 | 1088101 | C | T | upstream_gene_variant | MODIFIER | c.-1044C>T| |
S306 S308 |
| 154059 | BAA02g02450 | A02 | 1088617 | G | A | upstream_gene_variant | MODIFIER | c.-528G>A| |
S205 |
| 154060 | BAA02g02450 | A02 | 1089540 | C | T | intron_variant | MODIFIER | c.188-43C>T| |
S42 |
| 154061 | BAA02g02450 | A02 | 1090212 | G | A | missense_variant | MODERATE | c.700G>A|p.Glu234Lys |
S62 |
| 154062 | BAA02g02450 | A02 | 1091897 | C | T | synonymous_variant | LOW | c.750C>T|p.Val250Val |
S130 |
| 154063 | BAA02g02450 | A02 | 1093015 | C | T | missense_variant | MODERATE | c.1868C>T|p.Pro623Leu |
S216 |
| 154064 | BAA02g02450 | A02 | 1094231 | C | T | downstream_gene_variant | MODIFIER | c.*17C>T| |
S243 S299 |
| 154065 | BAA02g02450 | A02 | 1094273 | G | A | downstream_gene_variant | MODIFIER | c.*59G>A| |
S296 S5 |
| 154066 | BAA02g02450 | A02 | 1094886 | C | T | downstream_gene_variant | MODIFIER | c.*672C>T| |
S283 |
| 154067 | BAA02g02450 | A02 | 1096421 | G | A | downstream_gene_variant | MODIFIER | c.*2207G>A| |
S95 |
| 154068 | BAA02g02460 | A02 | 1097106 | C | T | upstream_gene_variant | MODIFIER | c.-437G>A| |
S100 |
| 154069 | BAA02g02460 | A02 | 1098291 | C | T | upstream_gene_variant | MODIFIER | c.-1622G>A| |
S116 |
| 154070 | BAA02g02460 | A02 | 1099001 | C | T | upstream_gene_variant | MODIFIER | c.-2332G>A| |
S13 |
| 154071 | BAA02g02460 | A02 | 1099112 | G | A | upstream_gene_variant | MODIFIER | c.-2443C>T| |
S136 |
| 154072 | BAA02g02460 | A02 | 1100043 | C | T | upstream_gene_variant | MODIFIER | c.-3374G>A| |
S272 |
| 154073 | BAA02g02460 | A02 | 1101349 | C | T | upstream_gene_variant | MODIFIER | c.-4680G>A| |
S262 |
| 154074 | BAA02g02470 | A02 | 1102283 | G | A | upstream_gene_variant | MODIFIER | c.-1404G>A| |
S286 |
| 154075 | BAA02g02470 | A02 | 1103197 | C | T | upstream_gene_variant | MODIFIER | c.-490C>T| |
S193 |