Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06040 | A02 | 2563833 | G | A | upstream_gene_variant | MODIFIER | c.-1742G>A| |
S132 S137 S215 |
2 | BAA02g06040 | A02 | 2563923 | C | T | upstream_gene_variant | MODIFIER | c.-1652C>T| |
S132 S137 S138 S215 S237 S238 S288 S89 |
3 | BAA02g06040 | A02 | 2564705 | G | A | upstream_gene_variant | MODIFIER | c.-870G>A| |
S105 S106 |
4 | BAA02g06040 | A02 | 2567442 | G | A | intron_variant | MODIFIER | c.615+362G>A| |
S190 |
5 | BAA02g06040 | A02 | 2567853 | C | T | intron_variant | MODIFIER | c.615+773C>T| |
S230 |
6 | BAA02g06040 | A02 | 2568629 | G | A | intron_variant | MODIFIER | c.615+1549G>A| |
S203 |
7 | BAA02g06040 | A02 | 2568865 | C | T | intron_variant | MODIFIER | c.615+1785C>T| |
S298 |
8 | BAA02g06040 | A02 | 2571958 | C | T | synonymous_variant | LOW | c.747C>T|p.Leu249Leu |
S178 |
9 | BAA02g06040 | A02 | 2572079 | C | T | downstream_gene_variant | MODIFIER | c.*88C>T| |
S216 |