Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g47350 | A01 | 31566879 | C | T | missense_variant | MODERATE | c.685G>A|p.Ala229Thr |
S229 |
2 | BAA01g47350 | A01 | 31567642 | G | A | synonymous_variant | LOW | c.180C>T|p.Leu60Leu |
S133 |
3 | BAA01g47350 | A01 | 31572216 | G | A | upstream_gene_variant | MODIFIER | c.-4085C>T| |
S128 |
4 | BAA01g47350 | A01 | 31572298 | C | T | upstream_gene_variant | MODIFIER | c.-4167G>A| |
S190 |
5 | BAA01g47350 | A01 | 31572398 | C | T | upstream_gene_variant | MODIFIER | c.-4267G>A| |
S228 |
6 | BAA01g47350 | A01 | 31572638 | G | A | upstream_gene_variant | MODIFIER | c.-4507C>T| |
S79 S84 |