Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42190 | A02 | 35172968 | C | T | downstream_gene_variant | MODIFIER | c.*4613G>A| |
S16 |
2 | BAA02g42190 | A02 | 35174144 | G | A | downstream_gene_variant | MODIFIER | c.*3437C>T| |
S142 |
3 | BAA02g42190 | A02 | 35174451 | G | A | downstream_gene_variant | MODIFIER | c.*3130C>T| |
S11 |
4 | BAA02g42190 | A02 | 35175263 | C | T | downstream_gene_variant | MODIFIER | c.*2318G>A| |
S33 |
5 | BAA02g42190 | A02 | 35175916 | C | T | downstream_gene_variant | MODIFIER | c.*1665G>A| |
S120 |
6 | BAA02g42190 | A02 | 35176774 | G | A | downstream_gene_variant | MODIFIER | c.*807C>T| |
S143 |
7 | BAA02g42190 | A02 | 35177186 | G | A | downstream_gene_variant | MODIFIER | c.*395C>T| |
S210 S225 |
8 | BAA02g42190 | A02 | 35177921 | C | T | missense_variant | MODERATE | c.530G>A|p.Arg177Lys |
S182 |
9 | BAA02g42190 | A02 | 35178745 | C | T | missense_variant | MODERATE | c.8G>A|p.Arg3Lys |
S72 S78 |
10 | BAA02g42190 | A02 | 35179338 | C | T | upstream_gene_variant | MODIFIER | c.-586G>A| |
S182 |
11 | BAA02g42190 | A02 | 35180423 | C | T | upstream_gene_variant | MODIFIER | c.-1671G>A| |
S18 |
12 | BAA02g42190 | A02 | 35180462 | C | T | upstream_gene_variant | MODIFIER | c.-1710G>A| |
S271 |
13 | BAA02g42190 | A02 | 35183656 | G | A | upstream_gene_variant | MODIFIER | c.-4904C>T| |
S103 |