Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13380 | A02 | 6090163 | C | T | downstream_gene_variant | MODIFIER | c.*1731G>A| |
S179 |
2 | BAA02g13380 | A02 | 6091754 | G | A | downstream_gene_variant | MODIFIER | c.*140C>T| |
S153 S157 S166 S257 |
3 | BAA02g13380 | A02 | 6092761 | G | A | missense_variant | MODERATE | c.1067C>T|p.Pro356Leu |
S204 |
4 | BAA02g13380 | A02 | 6092849 | C | T | missense_variant | MODERATE | c.979G>A|p.Glu327Lys |
S121 |
5 | BAA02g13380 | A02 | 6094623 | C | T | missense_variant | MODERATE | c.62G>A|p.Gly21Asp |
S263 |
6 | BAA02g13380 | A02 | 6094681 | C | T | missense_variant | MODERATE | c.4G>A|p.Gly2Arg |
S308 |
7 | BAA02g13380 | A02 | 6095815 | G | A | upstream_gene_variant | MODIFIER | c.-1131C>T| |
S43 |
8 | BAA02g13380 | A02 | 6095940 | G | A | upstream_gene_variant | MODIFIER | c.-1256C>T| |
S68 |
9 | BAA02g13380 | A02 | 6096747 | C | T | upstream_gene_variant | MODIFIER | c.-2063G>A| |
S272 |
10 | BAA02g13380 | A02 | 6099060 | C | T | upstream_gene_variant | MODIFIER | c.-4376G>A| |
S44 |