Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47780 | A09 | 51893084 | C | T | missense_variant | MODERATE | c.1696G>A|p.Glu566Lys |
S286 |
2 | BAA09g47780 | A09 | 51893311 | C | T | missense_variant | MODERATE | c.1469G>A|p.Gly490Asp |
S224 |
3 | BAA09g47780 | A09 | 51893880 | C | T | synonymous_variant | LOW | c.900G>A|p.Lys300Lys |
S82 S92 |
4 | BAA09g47780 | A09 | 51894335 | C | T | missense_variant | MODERATE | c.445G>A|p.Glu149Lys |
S5 |
5 | BAA09g47780 | A09 | 51897791 | G | A | upstream_gene_variant | MODIFIER | c.-3012C>T| |
S127 |
6 | BAA09g47780 | A09 | 51898525 | G | A | upstream_gene_variant | MODIFIER | c.-3746C>T| |
S54 |
7 | BAA09g47780 | A09 | 51898673 | C | T | upstream_gene_variant | MODIFIER | c.-3894G>A| |
S163 |
8 | BAA09g47780 | A09 | 51899186 | G | A | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S11 |