Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50860 | A09 | 53521270 | C | T | intron_variant | MODIFIER | c.1240-16C>T| |
S282 |
2 | BAA09g50860 | A09 | 53521371 | G | A | missense_variant | MODERATE | c.1325G>A|p.Arg442Lys |
S126 |
3 | BAA09g50860 | A09 | 53521482 | G | A | intron_variant | MODIFIER | c.1396-31G>A| |
S262 |
4 | BAA09g50860 | A09 | 53522573 | C | T | downstream_gene_variant | MODIFIER | c.*695C>T| |
S153 |
5 | BAA09g50860 | A09 | 53522770 | G | A | downstream_gene_variant | MODIFIER | c.*892G>A| |
S36 |
6 | BAA09g50860 | A09 | 53522940 | G | A | downstream_gene_variant | MODIFIER | c.*1062G>A| |
S262 |
7 | BAA09g50860 | A09 | 53524320 | C | T | downstream_gene_variant | MODIFIER | c.*2442C>T| |
S303 |
8 | BAA09g50860 | A09 | 53524556 | C | T | downstream_gene_variant | MODIFIER | c.*2678C>T| |
S18 |