Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g40590 | A09 | 47653349 | C | T | missense_variant | MODERATE | c.416G>A|p.Gly139Asp |
S119 |
2 | BAA09g40590 | A09 | 47654584 | G | A | upstream_gene_variant | MODIFIER | c.-603C>T| |
S87 |
3 | BAA09g40590 | A09 | 47655718 | C | T | upstream_gene_variant | MODIFIER | c.-1737G>A| |
S293 |
4 | BAA09g40590 | A09 | 47656394 | G | A | upstream_gene_variant | MODIFIER | c.-2413C>T| |
S98 |
5 | BAA09g40590 | A09 | 47656730 | C | T | upstream_gene_variant | MODIFIER | c.-2749G>A| |
S237 |
6 | BAA09g40590 | A09 | 47658020 | C | T | upstream_gene_variant | MODIFIER | c.-4039G>A| |
S90 |
7 | BAA09g40590 | A09 | 47658240 | C | T | upstream_gene_variant | MODIFIER | c.-4259G>A| |
S20 |