Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11080 | A02 | 5004120 | C | T | downstream_gene_variant | MODIFIER | c.*3367G>A| |
S124 |
2 | BAA02g11080 | A02 | 5004996 | G | A | downstream_gene_variant | MODIFIER | c.*2491C>T| |
S271 |
3 | BAA02g11080 | A02 | 5006514 | C | T | downstream_gene_variant | MODIFIER | c.*973G>A| |
S71 |
4 | BAA02g11080 | A02 | 5006647 | G | A | downstream_gene_variant | MODIFIER | c.*840C>T| |
S80 |
5 | BAA02g11080 | A02 | 5006797 | A | G | downstream_gene_variant | MODIFIER | c.*690T>C| |
S117 |
6 | BAA02g11080 | A02 | 5006981 | C | T | downstream_gene_variant | MODIFIER | c.*506G>A| |
S64 |
7 | BAA02g11080 | A02 | 5007071 | G | A | downstream_gene_variant | MODIFIER | c.*416C>T| |
S177 |
8 | BAA02g11080 | A02 | 5007349 | C | T | downstream_gene_variant | MODIFIER | c.*138G>A| |
S270 |
9 | BAA02g11080 | A02 | 5007750 | C | T | missense_variant | MODERATE | c.160G>A|p.Val54Met |
S34 |
10 | BAA02g11080 | A02 | 5008316 | G | A | upstream_gene_variant | MODIFIER | c.-407C>T| |
S203 |
11 | BAA02g11080 | A02 | 5008431 | G | A | upstream_gene_variant | MODIFIER | c.-522C>T| |
S59 |
12 | BAA02g11080 | A02 | 5009388 | C | T | upstream_gene_variant | MODIFIER | c.-1479G>A| |
S243 |