Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g28300 | A02 | 15897085 | C | T | missense_variant | MODERATE | c.1171G>A|p.Ala391Thr |
S9 |
2 | BAA02g28300 | A02 | 15897140 | G | A | synonymous_variant | LOW | c.1116C>T|p.Asp372Asp |
S34 |
3 | BAA02g28300 | A02 | 15898001 | C | T | synonymous_variant | LOW | c.597G>A|p.Arg199Arg |
S305 |
4 | BAA02g28300 | A02 | 15898747 | C | T | missense_variant&splice_region_variant | MODERATE | c.314G>A|p.Gly105Asp |
S178 |
5 | BAA02g28300 | A02 | 15899554 | G | A | upstream_gene_variant | MODIFIER | c.-213C>T| |
S23 |
6 | BAA02g28300 | A02 | 15901359 | G | A | upstream_gene_variant | MODIFIER | c.-2018C>T| |
S68 |
7 | BAA02g28300 | A02 | 15902686 | A | T | upstream_gene_variant | MODIFIER | c.-3345T>A| |
S159 S243 |
8 | BAA02g28300 | A02 | 15903174 | G | A | upstream_gene_variant | MODIFIER | c.-3833C>T| |
S247 |