Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g25590 | A02 | 14037599 | C | T | synonymous_variant | LOW | c.168G>A|p.Thr56Thr |
S51 |
2 | BAA02g25590 | A02 | 14040881 | G | A | upstream_gene_variant | MODIFIER | c.-3115C>T| |
S126 |
3 | BAA02g25590 | A02 | 14040936 | G | A | upstream_gene_variant | MODIFIER | c.-3170C>T| |
S275 |
4 | BAA02g25590 | A02 | 14041068 | C | T | upstream_gene_variant | MODIFIER | c.-3302G>A| |
S266 |
5 | BAA02g25590 | A02 | 14041089 | G | A | upstream_gene_variant | MODIFIER | c.-3323C>T| |
S229 |
6 | BAA02g25590 | A02 | 14041232 | G | A | upstream_gene_variant | MODIFIER | c.-3466C>T| |
S206 S26 |
7 | BAA02g25590 | A02 | 14041617 | C | T | upstream_gene_variant | MODIFIER | c.-3851G>A| |
S8 |
8 | BAA02g25590 | A02 | 14041786 | C | T | upstream_gene_variant | MODIFIER | c.-4020G>A| |
S240 |
9 | BAA02g25590 | A02 | 14042033 | G | A | upstream_gene_variant | MODIFIER | c.-4267C>T| |
S188 |