Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19140 | A02 | 9938640 | G | A | upstream_gene_variant | MODIFIER | c.-931G>A| |
S19 S298 |
2 | BAA02g19140 | A02 | 9939833 | C | A | intron_variant | MODIFIER | c.161+12C>A| |
S122 S125 S138 S147 S161 S179 S18 S26 S288 S295 S37 S44 S84 |
3 | BAA02g19140 | A02 | 9940273 | C | T | downstream_gene_variant | MODIFIER | c.*296C>T| |
S163 |
4 | BAA02g19140 | A02 | 9941586 | G | A | downstream_gene_variant | MODIFIER | c.*1609G>A| |
S34 |
5 | BAA02g19140 | A02 | 9942220 | G | A | downstream_gene_variant | MODIFIER | c.*2243G>A| |
S172 S217 |
6 | BAA02g19140 | A02 | 9942806 | C | T | downstream_gene_variant | MODIFIER | c.*2829C>T| |
S77 S82 |
7 | BAA02g19140 | A02 | 9943174 | C | T | downstream_gene_variant | MODIFIER | c.*3197C>T| |
S15 S3 |
8 | BAA02g19140 | A02 | 9943750 | G | A | downstream_gene_variant | MODIFIER | c.*3773G>A| |
S139 |
9 | BAA02g19140 | A02 | 9944111 | G | A | downstream_gene_variant | MODIFIER | c.*4134G>A| |
S57 |