Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46050 | A02 | 37538940 | C | T | upstream_gene_variant | MODIFIER | c.-3645C>T| |
S183 S198 |
2 | BAA02g46050 | A02 | 37539103 | C | T | upstream_gene_variant | MODIFIER | c.-3482C>T| |
S188 |
3 | BAA02g46050 | A02 | 37539496 | C | T | upstream_gene_variant | MODIFIER | c.-3089C>T| |
S303 |
4 | BAA02g46050 | A02 | 37539795 | G | A | upstream_gene_variant | MODIFIER | c.-2790G>A| |
S125 |
5 | BAA02g46050 | A02 | 37541811 | C | T | upstream_gene_variant | MODIFIER | c.-774C>T| |
S273 |
6 | BAA02g46050 | A02 | 37542548 | C | T | upstream_gene_variant | MODIFIER | c.-37C>T| |
S68 |
7 | BAA02g46050 | A02 | 37542870 | G | A | missense_variant | MODERATE | c.286G>A|p.Glu96Lys |
S111 |
8 | BAA02g46050 | A02 | 37543247 | G | A | synonymous_variant | LOW | c.444G>A|p.Leu148Leu |
S148 S31 |
9 | BAA02g46050 | A02 | 37543828 | C | T | synonymous_variant | LOW | c.849C>T|p.His283His |
S46 |