| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 14301 | BAA01g11140 | A01 | 5142076 | G | A | upstream_gene_variant | MODIFIER | c.-1154G>A| |
S13 |
| 14302 | BAA01g11140 | A01 | 5143501 | C | T | missense_variant | MODERATE | c.272C>T|p.Ser91Leu |
S301 |
| 14303 | BAA01g11150 | A01 | 5146583 | C | T | missense_variant | MODERATE | c.122C>T|p.Ser41Leu |
S2 |
| 14304 | BAA01g11140 | A01 | 5146699 | G | A | downstream_gene_variant | MODIFIER | c.*1924G>A| |
S298 |
| 14305 | BAA01g11140 | A01 | 5146714 | C | T | downstream_gene_variant | MODIFIER | c.*1939C>T| |
S66 |
| 14306 | BAA01g11150 | A01 | 5147403 | G | A | missense_variant | MODERATE | c.607G>A|p.Ala203Thr |
S17 |
| 14307 | BAA01g11150 | A01 | 5147681 | G | A | synonymous_variant | LOW | c.885G>A|p.Gln295Gln |
S252 |
| 14308 | BAA01g11150 | A01 | 5148742 | G | A | synonymous_variant | LOW | c.1542G>A|p.Glu514Glu |
S12 |
| 14309 | BAA01g11140 | A01 | 5149531 | G | A | downstream_gene_variant | MODIFIER | c.*4756G>A| |
S208 S219 |
| 14310 | BAA01g11140 | A01 | 5149722 | C | T | downstream_gene_variant | MODIFIER | c.*4947C>T| |
S13 S168 S278 S279 S64 |
| 14311 | BAA01g11150 | A01 | 5152535 | G | A | downstream_gene_variant | MODIFIER | c.*3197G>A| |
S116 |
| 14312 | BAA01g11150 | A01 | 5152594 | T | C | downstream_gene_variant | MODIFIER | c.*3256T>C| |
S153 S257 |
| 14313 | BAA01g11160 | A01 | 5158143 | G | A | upstream_gene_variant | MODIFIER | c.-4994C>T| |
S239 |
| 14314 | BAA01g11170 | A01 | 5159427 | C | T | upstream_gene_variant | MODIFIER | c.-2062C>T| |
S19 |
| 14315 | BAA01g11170 | A01 | 5159740 | G | A | upstream_gene_variant | MODIFIER | c.-1749G>A| |
S11 |
| 14316 | BAA01g11170 | A01 | 5159914 | G | A | upstream_gene_variant | MODIFIER | c.-1575G>A| |
S174 |
| 14317 | BAA01g11170 | A01 | 5160197 | C | T | upstream_gene_variant | MODIFIER | c.-1292C>T| |
S176 |
| 14318 | BAA01g11170 | A01 | 5160473 | C | A | upstream_gene_variant | MODIFIER | c.-1016C>A| |
S26 |
| 14319 | BAA01g11170 | A01 | 5160939 | T | A | upstream_gene_variant | MODIFIER | c.-550T>A| |
S239 |
| 14320 | BAA01g11170 | A01 | 5161044 | A | G | upstream_gene_variant | MODIFIER | c.-445A>G| |
S25 S264 |
| 14321 | BAA01g11170 | A01 | 5161135 | C | T | upstream_gene_variant | MODIFIER | c.-354C>T| |
S67 |
| 14322 | BAA01g11190 | A01 | 5164717 | G | A | upstream_gene_variant | MODIFIER | c.-4621G>A| |
S121 |
| 14323 | BAA01g11180 | A01 | 5165157 | G | A | missense_variant | MODERATE | c.2222C>T|p.Pro741Leu |
S172 S217 |
| 14324 | BAA01g11180 | A01 | 5165419 | G | A | missense_variant | MODERATE | c.1960C>T|p.Pro654Ser |
S224 |
| 14325 | BAA01g11180 | A01 | 5166326 | G | A | synonymous_variant | LOW | c.1053C>T|p.Phe351Phe |
S8 |