Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09030 | A02 | 3993150 | C | T | synonymous_variant | LOW | c.1116G>A|p.Gln372Gln |
S75 S81 |
2 | BAA02g09030 | A02 | 3993474 | G | A | missense_variant | MODERATE | c.881C>T|p.Ala294Val |
S291 |
3 | BAA02g09030 | A02 | 3993493 | T | A | missense_variant | MODERATE | c.862A>T|p.Ile288Phe |
S255 |
4 | BAA02g09030 | A02 | 3993650 | G | A | synonymous_variant | LOW | c.705C>T|p.Ile235Ile |
S61 |
5 | BAA02g09030 | A02 | 3996969 | G | A | upstream_gene_variant | MODIFIER | c.-2385C>T| |
S229 |
6 | BAA02g09030 | A02 | 3997245 | C | T | upstream_gene_variant | MODIFIER | c.-2661G>A| |
S195 |
7 | BAA02g09030 | A02 | 3997969 | C | T | upstream_gene_variant | MODIFIER | c.-3385G>A| |
S56 |
8 | BAA02g09030 | A02 | 3998059 | C | T | upstream_gene_variant | MODIFIER | c.-3475G>A| |
S255 |
9 | BAA02g09030 | A02 | 3998761 | C | T | upstream_gene_variant | MODIFIER | c.-4177G>A| |
S277 |