Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39880 | A02 | 33755449 | C | T | upstream_gene_variant | MODIFIER | c.-3792C>T| |
S267 |
2 | BAA02g39880 | A02 | 33759299 | C | T | missense_variant | MODERATE | c.59C>T|p.Ala20Val |
S135 S152 S68 |
3 | BAA02g39880 | A02 | 33759349 | C | T | missense_variant | MODERATE | c.109C>T|p.Arg37Cys |
S33 |
4 | BAA02g39880 | A02 | 33759682 | G | A | missense_variant | MODERATE | c.442G>A|p.Ala148Thr |
S13 |
5 | BAA02g39880 | A02 | 33761387 | C | T | splice_region_variant&intron_variant | LOW | c.746-4C>T| |
S83 S88 |
6 | BAA02g39880 | A02 | 33761703 | C | T | missense_variant | MODERATE | c.1058C>T|p.Thr353Ile |
S19 |
7 | BAA02g39880 | A02 | 33762592 | G | A | downstream_gene_variant | MODIFIER | c.*711G>A| |
S127 |
8 | BAA02g39880 | A02 | 33765208 | G | A | downstream_gene_variant | MODIFIER | c.*3327G>A| |
S288 |
9 | BAA02g39880 | A02 | 33765331 | C | T | downstream_gene_variant | MODIFIER | c.*3450C>T| |
S195 |
10 | BAA02g39880 | A02 | 33765338 | G | A | downstream_gene_variant | MODIFIER | c.*3457G>A| |
S169 |