Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28850 | A02 | 16241861 | G | A | stop_gained | HIGH | c.92G>A|p.Trp31* |
S125 |
2 | BAA02g28850 | A02 | 16242173 | G | A | missense_variant | MODERATE | c.323G>A|p.Gly108Glu |
S259 |
3 | BAA02g28850 | A02 | 16243298 | G | A | missense_variant | MODERATE | c.1027G>A|p.Val343Ile |
S7 |
4 | BAA02g28850 | A02 | 16243492 | C | T | splice_region_variant&intron_variant | LOW | c.1131+4C>T| |
S105 S106 |
5 | BAA02g28850 | A02 | 16243985 | G | A | missense_variant | MODERATE | c.1423G>A|p.Asp475Asn |
S173 |
6 | BAA02g28850 | A02 | 16247222 | C | T | downstream_gene_variant | MODIFIER | c.*3148C>T| |
S177 |
7 | BAA02g28850 | A02 | 16247765 | G | A | downstream_gene_variant | MODIFIER | c.*3691G>A| |
S148 S210 S30 S31 |
8 | BAA02g28850 | A02 | 16247902 | C | T | downstream_gene_variant | MODIFIER | c.*3828C>T| |
S51 |
9 | BAA02g28850 | A02 | 16247966 | G | A | downstream_gene_variant | MODIFIER | c.*3892G>A| |
S247 |
10 | BAA02g28850 | A02 | 16247967 | C | T | downstream_gene_variant | MODIFIER | c.*3893C>T| |
S157 S163 |
11 | BAA02g28850 | A02 | 16249014 | G | A | downstream_gene_variant | MODIFIER | c.*4940G>A| |
S279 |