Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g25600 | A09 | 16511447 | C | T | missense_variant | MODERATE | c.2452G>A|p.Glu818Lys |
S41 |
2 | BAA09g25600 | A09 | 16512399 | G | A | missense_variant | MODERATE | c.1808C>T|p.Ala603Val |
S138 |
3 | BAA09g25600 | A09 | 16513688 | C | T | missense_variant | MODERATE | c.1388G>A|p.Gly463Glu |
S219 S72 |
4 | BAA09g25600 | A09 | 16513710 | C | T | missense_variant | MODERATE | c.1366G>A|p.Glu456Lys |
S282 |
5 | BAA09g25600 | A09 | 16515333 | T | A | missense_variant | MODERATE | c.287A>T|p.Glu96Val |
S264 |
6 | BAA09g25600 | A09 | 16515334 | C | A | stop_gained | HIGH | c.286G>T|p.Glu96* |
S264 |
7 | BAA09g25600 | A09 | 16518972 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S184 |
8 | BAA09g25600 | A09 | 16519490 | G | A | upstream_gene_variant | MODIFIER | c.-3871C>T| |
S132 S137 S215 |
9 | BAA09g25600 | A09 | 16519633 | C | T | upstream_gene_variant | MODIFIER | c.-4014G>A| |
S148 |