Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00910 | A02 | 421153 | G | A | missense_variant | MODERATE | c.245C>T|p.Thr82Ile |
S271 |
2 | BAA02g00910 | A02 | 423691 | G | A | upstream_gene_variant | MODIFIER | c.-2294C>T| |
S271 |
3 | BAA02g00910 | A02 | 423811 | C | T | upstream_gene_variant | MODIFIER | c.-2414G>A| |
S119 |
4 | BAA02g00910 | A02 | 424143 | G | A | upstream_gene_variant | MODIFIER | c.-2746C>T| |
S291 |
5 | BAA02g00910 | A02 | 424525 | C | T | upstream_gene_variant | MODIFIER | c.-3128G>A| |
S108 |
6 | BAA02g00910 | A02 | 425841 | G | A | upstream_gene_variant | MODIFIER | c.-4444C>T| |
S146 |
7 | BAA02g00910 | A02 | 425986 | C | T | upstream_gene_variant | MODIFIER | c.-4589G>A| |
S283 |
8 | BAA02g00910 | A02 | 426055 | G | A | upstream_gene_variant | MODIFIER | c.-4658C>T| |
S221 |