Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g22660 | A09 | 14232907 | G | A | upstream_gene_variant | MODIFIER | c.-959G>A| |
S262 |
2 | BAA09g22660 | A09 | 14233651 | C | T | upstream_gene_variant | MODIFIER | c.-215C>T| |
S293 |
3 | BAA09g22660 | A09 | 14233882 | G | A | intron_variant | MODIFIER | c.8+9G>A| |
S196 |
4 | BAA09g22660 | A09 | 14234224 | G | A | intron_variant | MODIFIER | c.156+31G>A| |
S184 |
5 | BAA09g22660 | A09 | 14234498 | G | A | missense_variant | MODERATE | c.292G>A|p.Ala98Thr |
S98 |
6 | BAA09g22660 | A09 | 14236037 | C | T | stop_gained | HIGH | c.1258C>T|p.Gln420* |
S199 |
7 | BAA09g22660 | A09 | 14236124 | C | T | missense_variant | MODERATE | c.1345C>T|p.Pro449Ser |
S135 |
8 | BAA09g22660 | A09 | 14236262 | C | T | downstream_gene_variant | MODIFIER | c.*112C>T| |
S277 |