Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44500 | A02 | 36652801 | C | T | upstream_gene_variant | MODIFIER | c.-4936C>T| |
S260 |
2 | BAA02g44500 | A02 | 36653273 | G | A | upstream_gene_variant | MODIFIER | c.-4464G>A| |
S174 S27 |
3 | BAA02g44500 | A02 | 36654582 | G | A | upstream_gene_variant | MODIFIER | c.-3155G>A| |
S13 |
4 | BAA02g44500 | A02 | 36654670 | G | A | upstream_gene_variant | MODIFIER | c.-3067G>A| |
S261 |
5 | BAA02g44500 | A02 | 36656227 | C | T | upstream_gene_variant | MODIFIER | c.-1510C>T| |
S228 |
6 | BAA02g44500 | A02 | 36657257 | G | A | upstream_gene_variant | MODIFIER | c.-480G>A| |
S155 |
7 | BAA02g44500 | A02 | 36659052 | G | A | synonymous_variant | LOW | c.450G>A|p.Leu150Leu |
S272 |
8 | BAA02g44500 | A02 | 36659576 | C | T | missense_variant | MODERATE | c.734C>T|p.Thr245Ile |
S202 |