Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g11130 | A09 | 6180542 | C | T | synonymous_variant | LOW | c.537C>T|p.Asp179Asp |
S80 |
2 | BAA09g11130 | A09 | 6180600 | C | T | stop_gained | HIGH | c.595C>T|p.Gln199* |
S302 |
3 | BAA09g11130 | A09 | 6180729 | G | A | missense_variant | MODERATE | c.724G>A|p.Glu242Lys |
S210 S225 |
4 | BAA09g11130 | A09 | 6181280 | G | A | synonymous_variant | LOW | c.1275G>A|p.Arg425Arg |
S46 |
5 | BAA09g11130 | A09 | 6186120 | C | T | downstream_gene_variant | MODIFIER | c.*3931C>T| |
S287 |
6 | BAA09g11130 | A09 | 6186274 | G | A | downstream_gene_variant | MODIFIER | c.*4085G>A| |
S200 |
7 | BAA09g11130 | A09 | 6186687 | G | A | downstream_gene_variant | MODIFIER | c.*4498G>A| |
S192 |
8 | BAA09g11130 | A09 | 6186695 | G | A | downstream_gene_variant | MODIFIER | c.*4506G>A| |
S144 |
9 | BAA09g11130 | A09 | 6186861 | C | T | downstream_gene_variant | MODIFIER | c.*4672C>T| |
S33 |