Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44970 | A02 | 36937334 | C | T | upstream_gene_variant | MODIFIER | c.-4949C>T| |
S203 |
2 | BAA02g44970 | A02 | 36938274 | G | A | upstream_gene_variant | MODIFIER | c.-4009G>A| |
S45 |
3 | BAA02g44970 | A02 | 36938328 | C | T | upstream_gene_variant | MODIFIER | c.-3955C>T| |
S278 |
4 | BAA02g44970 | A02 | 36938431 | C | T | upstream_gene_variant | MODIFIER | c.-3852C>T| |
S283 |
5 | BAA02g44970 | A02 | 36939184 | G | A | upstream_gene_variant | MODIFIER | c.-3099G>A| |
S10 |
6 | BAA02g44970 | A02 | 36939322 | C | T | upstream_gene_variant | MODIFIER | c.-2961C>T| |
S58 |
7 | BAA02g44970 | A02 | 36939860 | G | A | upstream_gene_variant | MODIFIER | c.-2423G>A| |
S268 |
8 | BAA02g44970 | A02 | 36940369 | C | T | upstream_gene_variant | MODIFIER | c.-1914C>T| |
S259 |
9 | BAA02g44970 | A02 | 36941595 | C | T | upstream_gene_variant | MODIFIER | c.-688C>T| |
S107 |
10 | BAA02g44970 | A02 | 36941794 | G | A | upstream_gene_variant | MODIFIER | c.-489G>A| |
S10 |
11 | BAA02g44970 | A02 | 36942562 | C | T | intron_variant | MODIFIER | c.133+147C>T| |
S194 |
12 | BAA02g44970 | A02 | 36942854 | C | T | synonymous_variant | LOW | c.181C>T|p.Leu61Leu |
S95 |
13 | BAA02g44970 | A02 | 36943790 | T | A | intron_variant | MODIFIER | c.263+854T>A| |
S237 |
14 | BAA02g44970 | A02 | 36945023 | G | A | intron_variant | MODIFIER | c.264-513G>A| |
S246 |
15 | BAA02g44970 | A02 | 36945259 | G | A | intron_variant | MODIFIER | c.264-277G>A| |
S25 |
16 | BAA02g44970 | A02 | 36945581 | G | A | synonymous_variant | LOW | c.309G>A|p.Glu103Glu |
S11 |