Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g18270 | A09 | 10949898 | C | T | missense_variant | MODERATE | c.1519G>A|p.Glu507Lys |
S132 S137 S215 S89 |
2 | BAA09g18270 | A09 | 10951823 | G | A | missense_variant | MODERATE | c.572C>T|p.Pro191Leu |
S308 |
3 | BAA09g18270 | A09 | 10952683 | G | A | missense_variant | MODERATE | c.122C>T|p.Pro41Leu |
S237 |
4 | BAA09g18270 | A09 | 10952687 | C | T | missense_variant | MODERATE | c.118G>A|p.Val40Met |
S133 |
5 | BAA09g18270 | A09 | 10952765 | A | C | missense_variant | MODERATE | c.40T>G|p.Ser14Ala |
S171 |
6 | BAA09g18270 | A09 | 10953416 | G | A | upstream_gene_variant | MODIFIER | c.-612C>T| |
S174 S241 S27 S39 |
7 | BAA09g18270 | A09 | 10953550 | G | A | upstream_gene_variant | MODIFIER | c.-746C>T| |
S23 |
8 | BAA09g18270 | A09 | 10953979 | C | T | upstream_gene_variant | MODIFIER | c.-1175G>A| |
S8 |