Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30690 | A02 | 18077476 | C | T | missense_variant | MODERATE | c.91C>T|p.Pro31Ser |
S233 |
2 | BAA02g30690 | A02 | 18078414 | C | T | intron_variant | MODIFIER | c.746+17C>T| |
S15 S3 |
3 | BAA02g30690 | A02 | 18079576 | G | A | downstream_gene_variant | MODIFIER | c.*853G>A| |
S67 |
4 | BAA02g30690 | A02 | 18079647 | G | A | downstream_gene_variant | MODIFIER | c.*924G>A| |
S197 |
5 | BAA02g30690 | A02 | 18080379 | G | A | downstream_gene_variant | MODIFIER | c.*1656G>A| |
S126 |
6 | BAA02g30690 | A02 | 18080604 | C | T | downstream_gene_variant | MODIFIER | c.*1881C>T| |
S212 |
7 | BAA02g30690 | A02 | 18081418 | G | A | downstream_gene_variant | MODIFIER | c.*2695G>A| |
S166 |
8 | BAA02g30690 | A02 | 18081776 | G | A | downstream_gene_variant | MODIFIER | c.*3053G>A| |
S70 |
9 | BAA02g30690 | A02 | 18083113 | C | T | downstream_gene_variant | MODIFIER | c.*4390C>T| |
S296 |
10 | BAA02g30690 | A02 | 18083268 | C | T | downstream_gene_variant | MODIFIER | c.*4545C>T| |
S82 S92 |
11 | BAA02g30690 | A02 | 18083620 | G | A | downstream_gene_variant | MODIFIER | c.*4897G>A| |
S146 |