Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g05900 | A02 | 2508101 | C | T | stop_gained | HIGH | c.813G>A|p.Trp271* |
S25 |
2 | BAA02g05900 | A02 | 2508626 | C | T | missense_variant | MODERATE | c.524G>A|p.Gly175Glu |
S181 |
3 | BAA02g05900 | A02 | 2508686 | C | T | missense_variant | MODERATE | c.464G>A|p.Arg155His |
S121 |
4 | BAA02g05900 | A02 | 2509183 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.281-1G>A| |
S33 |
5 | BAA02g05900 | A02 | 2512967 | C | T | upstream_gene_variant | MODIFIER | c.-3197G>A| |
S152 |
6 | BAA02g05900 | A02 | 2513488 | C | T | upstream_gene_variant | MODIFIER | c.-3718G>A| |
S240 |