Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44180 | A09 | 49957427 | G | A | splice_region_variant&intron_variant | LOW | c.450-7G>A| |
S62 |
2 | BAA09g44180 | A09 | 49957571 | G | A | missense_variant | MODERATE | c.587G>A|p.Arg196His |
S224 S282 |
3 | BAA09g44180 | A09 | 49957582 | G | A | missense_variant | MODERATE | c.598G>A|p.Ala200Thr |
S274 |
4 | BAA09g44180 | A09 | 49957659 | G | A | synonymous_variant | LOW | c.675G>A|p.Thr225Thr |
S271 |
5 | BAA09g44180 | A09 | 49957781 | C | T | missense_variant | MODERATE | c.797C>T|p.Ala266Val |
S168 |
6 | BAA09g44180 | A09 | 49958144 | C | T | missense_variant | MODERATE | c.1160C>T|p.Ala387Val |
S55 |
7 | BAA09g44180 | A09 | 49958310 | C | T | synonymous_variant | LOW | c.1326C>T|p.Ile442Ile |
S275 |
8 | BAA09g44180 | A09 | 49961359 | G | A | downstream_gene_variant | MODIFIER | c.*2530G>A| |
S161 |
9 | BAA09g44180 | A09 | 49961399 | C | T | downstream_gene_variant | MODIFIER | c.*2570C>T| |
S302 |
10 | BAA09g44180 | A09 | 49963029 | C | T | downstream_gene_variant | MODIFIER | c.*4200C>T| |
S32 |
11 | BAA09g44180 | A09 | 49963425 | C | T | downstream_gene_variant | MODIFIER | c.*4596C>T| |
S32 |