Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g07530 | A02 | 3228186 | G | A | missense_variant | MODERATE | c.2089C>T|p.Arg697Cys |
S276 |
2 | BAA02g07530 | A02 | 3228975 | C | T | missense_variant | MODERATE | c.1652G>A|p.Arg551Lys |
S135 |
3 | BAA02g07530 | A02 | 3230455 | C | T | stop_gained | HIGH | c.1056G>A|p.Trp352* |
S123 |
4 | BAA02g07530 | A02 | 3231938 | C | T | missense_variant | MODERATE | c.758G>A|p.Arg253Lys |
S46 |
5 | BAA02g07530 | A02 | 3232218 | G | A | missense_variant | MODERATE | c.478C>T|p.Pro160Ser |
S232 |
6 | BAA02g07530 | A02 | 3232369 | C | T | synonymous_variant | LOW | c.327G>A|p.Gly109Gly |
S46 |
7 | BAA02g07530 | A02 | 3233858 | C | T | upstream_gene_variant | MODIFIER | c.-646G>A| |
S212 |
8 | BAA02g07530 | A02 | 3237138 | C | T | upstream_gene_variant | MODIFIER | c.-3926G>A| |
S19 |
9 | BAA02g07530 | A02 | 3237226 | G | A | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S4 |
10 | BAA02g07530 | A02 | 3237462 | G | A | upstream_gene_variant | MODIFIER | c.-4250C>T| |
S244 |
11 | BAA02g07530 | A02 | 3237468 | G | A | upstream_gene_variant | MODIFIER | c.-4256C>T| |
S68 |