Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47490 | A09 | 51758711 | C | T | missense_variant | MODERATE | c.139C>T|p.Leu47Phe |
S237 |
2 | BAA09g47490 | A09 | 51758851 | G | A | stop_gained | HIGH | c.279G>A|p.Trp93* |
S45 |
3 | BAA09g47490 | A09 | 51759182 | G | A | downstream_gene_variant | MODIFIER | c.*58G>A| |
S128 |
4 | BAA09g47490 | A09 | 51759264 | G | A | downstream_gene_variant | MODIFIER | c.*140G>A| |
S178 S246 |
5 | BAA09g47490 | A09 | 51759404 | C | T | downstream_gene_variant | MODIFIER | c.*280C>T| |
S13 S168 S278 S279 |
6 | BAA09g47490 | A09 | 51761244 | C | T | downstream_gene_variant | MODIFIER | c.*2120C>T| |
S77 |
7 | BAA09g47490 | A09 | 51761405 | C | T | downstream_gene_variant | MODIFIER | c.*2281C>T| |
S19 |