| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA09g41250 | A09 | 48072791 | G | A | upstream_gene_variant | MODIFIER | c.-3998G>A| |
S45 |
| 2 | BAA09g41250 | A09 | 48073943 | C | T | upstream_gene_variant | MODIFIER | c.-2846C>T| |
S100 |
| 3 | BAA09g41250 | A09 | 48073946 | G | A | upstream_gene_variant | MODIFIER | c.-2843G>A| |
S270 |
| 4 | BAA09g41250 | A09 | 48074267 | G | A | upstream_gene_variant | MODIFIER | c.-2522G>A| |
S10 |
| 5 | BAA09g41250 | A09 | 48075345 | C | T | upstream_gene_variant | MODIFIER | c.-1444C>T| |
S294 |
| 6 | BAA09g41250 | A09 | 48076235 | G | A | upstream_gene_variant | MODIFIER | c.-554G>A| |
S127 |
| 7 | BAA09g41250 | A09 | 48076256 | G | A | upstream_gene_variant | MODIFIER | c.-533G>A| |
S181 |
| 8 | BAA09g41250 | A09 | 48076749 | C | T | upstream_gene_variant | MODIFIER | c.-40C>T| |
S191 |
| 9 | BAA09g41250 | A09 | 48076842 | G | A | synonymous_variant | LOW | c.54G>A|p.Pro18Pro |
S268 |
| 10 | BAA09g41250 | A09 | 48077630 | C | T | missense_variant | MODERATE | c.751C>T|p.Pro251Ser |
S5 |
| 11 | BAA09g41250 | A09 | 48077698 | C | T | synonymous_variant | LOW | c.819C>T|p.Phe273Phe |
S228 |
| 12 | BAA09g41250 | A09 | 48079356 | C | T | intron_variant | MODIFIER | c.1592+885C>T| |
S192 |
| 13 | BAA09g41250 | A09 | 48079358 | C | T | intron_variant | MODIFIER | c.1592+887C>T| |
S87 |
| 14 | BAA09g41250 | A09 | 48081210 | G | A | intron_variant | MODIFIER | c.1593-233G>A| |
S249 |
| 15 | BAA09g41250 | A09 | 48081897 | G | A | downstream_gene_variant | MODIFIER | c.*136G>A| |
S174 S216 S265 S27 |
| 16 | BAA09g41250 | A09 | 48082303 | C | T | downstream_gene_variant | MODIFIER | c.*542C>T| |
S20 |
| 17 | BAA09g41250 | A09 | 48084936 | G | A | downstream_gene_variant | MODIFIER | c.*3175G>A| |
S150 |
| 18 | BAA09g41250 | A09 | 48085845 | C | T | downstream_gene_variant | MODIFIER | c.*4084C>T| |
S118 |
| 19 | BAA09g41250 | A09 | 48086039 | C | T | downstream_gene_variant | MODIFIER | c.*4278C>T| |
S198 |