Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44270 | A02 | 36527535 | G | A | missense_variant | MODERATE | c.422C>T|p.Thr141Ile |
S94 |
2 | BAA02g44270 | A02 | 36529661 | G | A | upstream_gene_variant | MODIFIER | c.-840C>T| |
S5 |
3 | BAA02g44270 | A02 | 36531901 | G | A | upstream_gene_variant | MODIFIER | c.-3080C>T| |
S125 |
4 | BAA02g44270 | A02 | 36532051 | G | A | upstream_gene_variant | MODIFIER | c.-3230C>T| |
S143 S287 |
5 | BAA02g44270 | A02 | 36533081 | G | A | upstream_gene_variant | MODIFIER | c.-4260C>T| |
S56 |
6 | BAA02g44270 | A02 | 36533425 | G | A | upstream_gene_variant | MODIFIER | c.-4604C>T| |
S77 S82 |
7 | BAA02g44270 | A02 | 36533506 | C | T | upstream_gene_variant | MODIFIER | c.-4685G>A| |
S295 |