Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00970 | A02 | 451151 | C | T | downstream_gene_variant | MODIFIER | c.*407G>A| |
S287 |
2 | BAA02g00970 | A02 | 451400 | C | T | downstream_gene_variant | MODIFIER | c.*158G>A| |
S270 |
3 | BAA02g00970 | A02 | 451508 | C | T | downstream_gene_variant | MODIFIER | c.*50G>A| |
S177 |
4 | BAA02g00970 | A02 | 451774 | C | T | missense_variant | MODERATE | c.930G>A|p.Met310Ile |
S37 |
5 | BAA02g00970 | A02 | 453275 | G | A | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S247 |
6 | BAA02g00970 | A02 | 453446 | C | T | upstream_gene_variant | MODIFIER | c.-30G>A| |
S181 |
7 | BAA02g00970 | A02 | 454199 | C | T | upstream_gene_variant | MODIFIER | c.-783G>A| |
S104 |
8 | BAA02g00970 | A02 | 455045 | G | A | upstream_gene_variant | MODIFIER | c.-1629C>T| |
S289 S290 |
9 | BAA02g00970 | A02 | 457788 | G | A | upstream_gene_variant | MODIFIER | c.-4372C>T| |
S295 |
10 | BAA02g00970 | A02 | 458253 | C | T | upstream_gene_variant | MODIFIER | c.-4837G>A| |
S37 |