Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29700 | A02 | 17040058 | C | T | missense_variant | MODERATE | c.74G>A|p.Gly25Glu |
S185 |
2 | BAA02g29700 | A02 | 17040099 | C | T | splice_region_variant&intron_variant | LOW | c.40-7G>A| |
S301 S304 |
3 | BAA02g29700 | A02 | 17042140 | C | T | upstream_gene_variant | MODIFIER | c.-1928G>A| |
S231 |
4 | BAA02g29700 | A02 | 17042301 | C | T | upstream_gene_variant | MODIFIER | c.-2089G>A| |
S231 |
5 | BAA02g29700 | A02 | 17043523 | G | A | upstream_gene_variant | MODIFIER | c.-3311C>T| |
S199 |
6 | BAA02g29700 | A02 | 17044512 | C | T | upstream_gene_variant | MODIFIER | c.-4300G>A| |
S167 |
7 | BAA02g29700 | A02 | 17044812 | G | A | upstream_gene_variant | MODIFIER | c.-4600C>T| |
S259 |
8 | BAA02g29700 | A02 | 17044944 | C | T | upstream_gene_variant | MODIFIER | c.-4732G>A| |
S233 |
9 | BAA02g29700 | A02 | 17045192 | C | T | upstream_gene_variant | MODIFIER | c.-4980G>A| |
S107 |