| Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
|---|---|---|---|---|---|---|---|---|---|
| 40751 | BAA01g25760-BAA01g25770 | A01 | 14053039 | C | T | intergenic_region | MODIFIER | n.14053039C>T| |
S210 S225 |
| 40752 | BAA01g25760-BAA01g25770 | A01 | 14053150 | C | A | intergenic_region | MODIFIER | n.14053150C>A| |
S236 S242 S257 S267 S277 S94 |
| 40753 | BAA01g25760-BAA01g25770 | A01 | 14053797 | C | T | intergenic_region | MODIFIER | n.14053797C>T| |
S228 |
| 40754 | BAA01g25760-BAA01g25770 | A01 | 14053869 | G | C | intergenic_region | MODIFIER | n.14053869G>C| |
S210 |
| 40755 | BAA01g25760-BAA01g25770 | A01 | 14054665 | G | A | intergenic_region | MODIFIER | n.14054665G>A| |
S84 S93 |
| 40756 | BAA01g25760-BAA01g25770 | A01 | 14054717 | C | T | intergenic_region | MODIFIER | n.14054717C>T| |
S205 |
| 40757 | BAA01g25770 | A01 | 14055571 | C | T | upstream_gene_variant | MODIFIER | c.-4673C>T| |
S158 |
| 40758 | BAA01g25770 | A01 | 14055793 | C | T | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S19 |
| 40759 | BAA01g25770 | A01 | 14055993 | C | T | upstream_gene_variant | MODIFIER | c.-4251C>T| |
S54 |
| 40760 | BAA01g25770 | A01 | 14056677 | G | A | upstream_gene_variant | MODIFIER | c.-3567G>A| |
S126 |
| 40761 | BAA01g25770 | A01 | 14057170 | G | A | upstream_gene_variant | MODIFIER | c.-3074G>A| |
S232 |
| 40762 | BAA01g25770 | A01 | 14057224 | G | A | upstream_gene_variant | MODIFIER | c.-3020G>A| |
S100 |
| 40763 | BAA01g25770 | A01 | 14057562 | C | T | upstream_gene_variant | MODIFIER | c.-2682C>T| |
S176 |
| 40764 | BAA01g25770 | A01 | 14057812 | G | A | upstream_gene_variant | MODIFIER | c.-2432G>A| |
S195 |
| 40765 | BAA01g25770 | A01 | 14060938 | G | A | missense_variant | MODERATE | c.695G>A|p.Gly232Glu |
S72 S78 |
| 40766 | BAA01g25790 | A01 | 14062022 | G | A | upstream_gene_variant | MODIFIER | c.-3984G>A| |
S70 |
| 40767 | BAA01g25790 | A01 | 14062204 | C | T | upstream_gene_variant | MODIFIER | c.-3802C>T| |
S177 |
| 40768 | BAA01g25780 | A01 | 14062352 | G | A | missense_variant | MODERATE | c.182C>T|p.Ala61Val |
S37 |
| 40769 | BAA01g25780 | A01 | 14062456 | C | T | synonymous_variant | LOW | c.78G>A|p.Pro26Pro |
S159 S243 |
| 40770 | BAA01g25780 | A01 | 14063460 | C | T | upstream_gene_variant | MODIFIER | c.-927G>A| |
S143 S294 |
| 40771 | BAA01g25780 | A01 | 14063584 | C | T | upstream_gene_variant | MODIFIER | c.-1051G>A| |
S112 |
| 40772 | BAA01g25780 | A01 | 14063649 | C | T | upstream_gene_variant | MODIFIER | c.-1116G>A| |
S286 |
| 40773 | BAA01g25780 | A01 | 14063709 | G | A | upstream_gene_variant | MODIFIER | c.-1176C>T| |
S181 |
| 40774 | BAA01g25780 | A01 | 14063890 | G | A | upstream_gene_variant | MODIFIER | c.-1357C>T| |
S23 |
| 40775 | BAA01g25780 | A01 | 14064145 | C | T | upstream_gene_variant | MODIFIER | c.-1612G>A| |
S251 |