Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10540 | A02 | 4673986 | G | A | missense_variant | MODERATE | c.104C>T|p.Ser35Phe |
S209 |
2 | BAA02g10540 | A02 | 4674111 | G | A | upstream_gene_variant | MODIFIER | c.-22C>T| |
S295 |
3 | BAA02g10540 | A02 | 4674662 | C | T | upstream_gene_variant | MODIFIER | c.-573G>A| |
S179 |
4 | BAA02g10540 | A02 | 4674840 | C | T | upstream_gene_variant | MODIFIER | c.-751G>A| |
S202 |
5 | BAA02g10540 | A02 | 4676548 | C | T | upstream_gene_variant | MODIFIER | c.-2459G>A| |
S142 |
6 | BAA02g10540 | A02 | 4676791 | G | A | upstream_gene_variant | MODIFIER | c.-2702C>T| |
S98 |
7 | BAA02g10540 | A02 | 4677048 | C | T | upstream_gene_variant | MODIFIER | c.-2959G>A| |
S207 |
8 | BAA02g10540 | A02 | 4677311 | C | T | upstream_gene_variant | MODIFIER | c.-3222G>A| |
S268 |
9 | BAA02g10540 | A02 | 4677756 | G | A | upstream_gene_variant | MODIFIER | c.-3667C>T| |
S82 S92 |