| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 1 | BAA01g26890 | A01 | 15163090 | C | T | downstream_gene_variant | MODIFIER | c.*4887G>A| |
S206 S26 |
| 2 | BAA01g26890 | A01 | 15163419 | G | A | downstream_gene_variant | MODIFIER | c.*4558C>T| |
S60 |
| 3 | BAA01g26890 | A01 | 15163698 | G | A | downstream_gene_variant | MODIFIER | c.*4279C>T| |
S124 |
| 4 | BAA01g26890 | A01 | 15163803 | G | A | downstream_gene_variant | MODIFIER | c.*4174C>T| |
S162 |
| 5 | BAA01g26890 | A01 | 15164138 | G | A | downstream_gene_variant | MODIFIER | c.*3839C>T| |
S105 S106 |
| 6 | BAA01g26890 | A01 | 15164920 | G | A | downstream_gene_variant | MODIFIER | c.*3057C>T| |
S84 S93 |
| 7 | BAA01g26890 | A01 | 15165134 | C | T | downstream_gene_variant | MODIFIER | c.*2843G>A| |
S61 |
| 8 | BAA01g26890 | A01 | 15165258 | G | A | downstream_gene_variant | MODIFIER | c.*2719C>T| |
S266 |
| 9 | BAA01g26890 | A01 | 15165276 | C | T | downstream_gene_variant | MODIFIER | c.*2701G>A| |
S25 |
| 10 | BAA01g26890 | A01 | 15165756 | C | T | downstream_gene_variant | MODIFIER | c.*2221G>A| |
S38 |
| 11 | BAA01g26890 | A01 | 15166684 | C | T | downstream_gene_variant | MODIFIER | c.*1293G>A| |
S293 |
| 12 | BAA01g26890 | A01 | 15168559 | G | A | intron_variant | MODIFIER | c.227-188C>T| |
S144 |
| 13 | BAA01g26890 | A01 | 15169176 | G | A | intron_variant | MODIFIER | c.227-805C>T| |
S165 |
| 14 | BAA01g26890 | A01 | 15169319 | C | T | intron_variant | MODIFIER | c.227-948G>A| |
S166 |
| 15 | BAA01g26890 | A01 | 15170387 | C | T | intron_variant | MODIFIER | c.226+1090G>A| |
S267 |
| 16 | BAA01g26890 | A01 | 15170401 | C | T | intron_variant | MODIFIER | c.226+1076G>A| |
S177 |
| 17 | BAA01g26890 | A01 | 15170629 | C | T | intron_variant | MODIFIER | c.226+848G>A| |
S255 |
| 18 | BAA01g26890 | A01 | 15170856 | G | A | intron_variant | MODIFIER | c.226+621C>T| |
S275 |
| 19 | BAA01g26890 | A01 | 15171039 | C | T | intron_variant | MODIFIER | c.226+438G>A| |
S176 |
| 20 | BAA01g26890 | A01 | 15171379 | G | A | intron_variant | MODIFIER | c.226+98C>T| |
S157 |
| 21 | BAA01g26890 | A01 | 15171463 | G | A | intron_variant | MODIFIER | c.226+14C>T| |
S268 |
| 22 | BAA01g26890 | A01 | 15171928 | G | A | upstream_gene_variant | MODIFIER | c.-226C>T| |
S149 S62 |
| 23 | BAA01g26890 | A01 | 15172093 | C | T | upstream_gene_variant | MODIFIER | c.-391G>A| |
S135 |
| 24 | BAA01g26890 | A01 | 15173764 | G | A | upstream_gene_variant | MODIFIER | c.-2062C>T| |
S37 |
| 25 | BAA01g26890 | A01 | 15173842 | C | T | upstream_gene_variant | MODIFIER | c.-2140G>A| |
S261 |