Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11250 | A02 | 5074652 | G | A | missense_variant | MODERATE | c.208G>A|p.Glu70Lys |
S169 |
2 | BAA02g11250 | A02 | 5075163 | G | A | missense_variant | MODERATE | c.719G>A|p.Gly240Asp |
S247 |
3 | BAA02g11250 | A02 | 5075312 | G | A | missense_variant | MODERATE | c.868G>A|p.Ala290Thr |
S198 |
4 | BAA02g11250 | A02 | 5076161 | C | T | missense_variant | MODERATE | c.1661C>T|p.Pro554Leu |
S117 |
5 | BAA02g11250 | A02 | 5076247 | C | T | missense_variant | MODERATE | c.1747C>T|p.Pro583Ser |
S90 |
6 | BAA02g11250 | A02 | 5076319 | G | A | missense_variant | MODERATE | c.1819G>A|p.Gly607Arg |
S51 |
7 | BAA02g11250 | A02 | 5078874 | G | A | downstream_gene_variant | MODIFIER | c.*2436G>A| |
S166 |