Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47580 | A02 | 38315961 | G | A | missense_variant | MODERATE | c.1363C>T|p.Leu455Phe |
S30 |
2 | BAA02g47580 | A02 | 38316027 | G | A | missense_variant | MODERATE | c.1297C>T|p.His433Tyr |
S83 S88 |
3 | BAA02g47580 | A02 | 38317008 | G | A | splice_region_variant&intron_variant | LOW | c.727+8C>T| |
S204 |
4 | BAA02g47580 | A02 | 38317837 | C | T | missense_variant | MODERATE | c.386G>A|p.Cys129Tyr |
S190 |
5 | BAA02g47580 | A02 | 38318113 | C | T | missense_variant | MODERATE | c.110G>A|p.Arg37Lys |
S77 |
6 | BAA02g47580 | A02 | 38318314 | G | A | upstream_gene_variant | MODIFIER | c.-8C>T| |
S202 |
7 | BAA02g47580 | A02 | 38319291 | C | T | upstream_gene_variant | MODIFIER | c.-985G>A| |
S159 S243 |
8 | BAA02g47580 | A02 | 38319319 | G | A | upstream_gene_variant | MODIFIER | c.-1013C>T| |
S265 |
9 | BAA02g47580 | A02 | 38319550 | G | A | upstream_gene_variant | MODIFIER | c.-1244C>T| |
S204 |
10 | BAA02g47580 | A02 | 38322038 | G | A | upstream_gene_variant | MODIFIER | c.-3732C>T| |
S292 |
11 | BAA02g47580 | A02 | 38322982 | G | A | upstream_gene_variant | MODIFIER | c.-4676C>T| |
S298 |