Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g02010 | A02 | 894104 | G | A | missense_variant | MODERATE | c.1412C>T|p.Ala471Val |
S45 |
2 | BAA02g02010 | A02 | 894694 | C | T | stop_gained | HIGH | c.1101G>A|p.Trp367* |
S196 |
3 | BAA02g02010 | A02 | 894726 | G | A | missense_variant | MODERATE | c.1069C>T|p.His357Tyr |
S294 |
4 | BAA02g02010 | A02 | 895432 | C | T | missense_variant | MODERATE | c.622G>A|p.Val208Ile |
S117 |
5 | BAA02g02010 | A02 | 897777 | G | A | upstream_gene_variant | MODIFIER | c.-134C>T| |
S293 |
6 | BAA02g02010 | A02 | 898563 | C | T | upstream_gene_variant | MODIFIER | c.-920G>A| |
S133 |
7 | BAA02g02010 | A02 | 899042 | G | A | upstream_gene_variant | MODIFIER | c.-1399C>T| |
S265 |
8 | BAA02g02010 | A02 | 902048 | G | A | upstream_gene_variant | MODIFIER | c.-4405C>T| |
S165 |
9 | BAA02g02010 | A02 | 902530 | C | T | upstream_gene_variant | MODIFIER | c.-4887G>A| |
S51 |