Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34600 | A02 | 29678592 | G | A | downstream_gene_variant | MODIFIER | c.*3808C>T| |
S297 |
2 | BAA02g34600 | A02 | 29678718 | C | T | downstream_gene_variant | MODIFIER | c.*3682G>A| |
S18 |
3 | BAA02g34600 | A02 | 29678856 | C | T | downstream_gene_variant | MODIFIER | c.*3544G>A| |
S183 S198 |
4 | BAA02g34600 | A02 | 29679410 | C | T | downstream_gene_variant | MODIFIER | c.*2990G>A| |
S148 S210 |
5 | BAA02g34600 | A02 | 29680536 | C | G | downstream_gene_variant | MODIFIER | c.*1864G>C| |
S121 |
6 | BAA02g34600 | A02 | 29681238 | C | T | downstream_gene_variant | MODIFIER | c.*1162G>A| |
S259 |
7 | BAA02g34600 | A02 | 29681303 | C | T | downstream_gene_variant | MODIFIER | c.*1097G>A| |
S206 |
8 | BAA02g34600 | A02 | 29689473 | C | T | intron_variant | MODIFIER | c.438+1078G>A| |
S218 |
9 | BAA02g34600 | A02 | 29689660 | C | T | intron_variant | MODIFIER | c.438+891G>A| |
S135 |
10 | BAA02g34600 | A02 | 29689692 | G | A | intron_variant | MODIFIER | c.438+859C>T| |
S28 |
11 | BAA02g34600 | A02 | 29690948 | C | T | missense_variant | MODERATE | c.119G>A|p.Gly40Glu |
S2 |
12 | BAA02g34600 | A02 | 29691359 | C | T | upstream_gene_variant | MODIFIER | c.-293G>A| |
S18 S202 |
13 | BAA02g34600 | A02 | 29691558 | G | A | upstream_gene_variant | MODIFIER | c.-492C>T| |
S80 |
14 | BAA02g34600 | A02 | 29693489 | G | A | upstream_gene_variant | MODIFIER | c.-2423C>T| |
S159 S243 |