| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 199451 | BAA02g30090 | A02 | 17454090 | G | A | upstream_gene_variant | MODIFIER | c.-2763C>T| |
S157 |
| 199452 | BAA02g30100 | A02 | 17457244 | C | T | upstream_gene_variant | MODIFIER | c.-2415C>T| |
S138 |
| 199453 | BAA02g30100 | A02 | 17457440 | G | A | upstream_gene_variant | MODIFIER | c.-2219G>A| |
S290 |
| 199454 | BAA02g30100 | A02 | 17457946 | G | A | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S197 |
| 199455 | BAA02g30100 | A02 | 17459109 | G | A | upstream_gene_variant | MODIFIER | c.-550G>A| |
S287 |
| 199456 | BAA02g30100 | A02 | 17459313 | G | A | upstream_gene_variant | MODIFIER | c.-346G>A| |
S186 |
| 199457 | BAA02g30100 | A02 | 17460109 | G | A | synonymous_variant | LOW | c.225G>A|p.Glu75Glu |
S26 |
| 199458 | BAA02g30100 | A02 | 17460967 | C | T | downstream_gene_variant | MODIFIER | c.*798C>T| |
S219 S72 |
| 199459 | BAA02g30100 | A02 | 17461649 | G | A | downstream_gene_variant | MODIFIER | c.*1480G>A| |
S148 S210 S30 S31 |
| 199460 | BAA02g30100 | A02 | 17463625 | C | G | downstream_gene_variant | MODIFIER | c.*3456C>G| |
S211 S227 |
| 199461 | BAA02g30100 | A02 | 17464054 | C | T | downstream_gene_variant | MODIFIER | c.*3885C>T| |
S92 |
| 199462 | BAA02g30100 | A02 | 17464261 | G | A | downstream_gene_variant | MODIFIER | c.*4092G>A| |
S188 |
| 199463 | BAA02g30110 | A02 | 17467463 | C | T | downstream_gene_variant | MODIFIER | c.*1631G>A| |
S165 S211 S227 |
| 199464 | BAA02g30110 | A02 | 17467572 | C | T | downstream_gene_variant | MODIFIER | c.*1522G>A| |
S182 |
| 199465 | BAA02g30110 | A02 | 17470350 | G | A | missense_variant | MODERATE | c.424C>T|p.Pro142Ser |
S261 |
| 199466 | BAA02g30110 | A02 | 17471204 | C | T | upstream_gene_variant | MODIFIER | c.-431G>A| |
S38 |
| 199467 | BAA02g30110 | A02 | 17471795 | C | T | upstream_gene_variant | MODIFIER | c.-1022G>A| |
S9 |
| 199468 | BAA02g30120 | A02 | 17476074 | C | T | missense_variant | MODERATE | c.427G>A|p.Gly143Arg |
S83 S88 |
| 199469 | BAA02g30120 | A02 | 17476378 | G | A | synonymous_variant | LOW | c.123C>T|p.Ile41Ile |
S80 |
| 199470 | BAA02g30120 | A02 | 17476435 | G | A | synonymous_variant | LOW | c.66C>T|p.Val22Val |
S133 |
| 199471 | BAA02g30130 | A02 | 17478214 | C | T | missense_variant | MODERATE | c.575G>A|p.Arg192His |
S112 |
| 199472 | BAA02g30130 | A02 | 17478245 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.545-1G>A| |
S177 |
| 199473 | BAA02g30120 | A02 | 17478286 | C | T | upstream_gene_variant | MODIFIER | c.-1786G>A| |
S130 |
| 199474 | BAA02g30130 | A02 | 17478379 | G | A | missense_variant | MODERATE | c.475C>T|p.Leu159Phe |
S247 |
| 199475 | BAA02g30130 | A02 | 17478426 | G | A | missense_variant | MODERATE | c.428C>T|p.Pro143Leu |
S197 |