Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g50780 | A09 | 53490682 | G | A | missense_variant | MODERATE | c.889C>T|p.Pro297Ser |
S150 |
2 | BAA09g50780 | A09 | 53492400 | C | T | missense_variant | MODERATE | c.317G>A|p.Gly106Asp |
S94 |
3 | BAA09g50780 | A09 | 53492968 | C | T | missense_variant | MODERATE | c.221G>A|p.Arg74His |
S134 |
4 | BAA09g50780 | A09 | 53495276 | C | T | upstream_gene_variant | MODIFIER | c.-1457G>A| |
S226 |
5 | BAA09g50780 | A09 | 53495394 | G | A | upstream_gene_variant | MODIFIER | c.-1575C>T| |
S132 S137 S215 S89 |
6 | BAA09g50780 | A09 | 53495472 | G | A | upstream_gene_variant | MODIFIER | c.-1653C>T| |
S46 |