Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17880 | A01 | 8697995 | G | A | upstream_gene_variant | MODIFIER | c.-3344G>A| |
S187 |
2 | BAA01g17880 | A01 | 8701529 | G | A | splice_region_variant&intron_variant | LOW | c.186+5G>A| |
S138 |
3 | BAA01g17880 | A01 | 8701937 | G | A | splice_region_variant&intron_variant | LOW | c.351+5G>A| |
S203 |
4 | BAA01g17880 | A01 | 8702529 | G | A | missense_variant | MODERATE | c.538G>A|p.Ala180Thr |
S240 |
5 | BAA01g17880 | A01 | 8703133 | C | T | splice_region_variant&intron_variant | LOW | c.646-3C>T| |
S215 |
6 | BAA01g17880 | A01 | 8703190 | G | A | missense_variant | MODERATE | c.700G>A|p.Asp234Asn |
S278 |
7 | BAA01g17880 | A01 | 8704292 | G | A | missense_variant | MODERATE | c.1204G>A|p.Ala402Thr |
S207 |
8 | BAA01g17880 | A01 | 8708428 | C | T | downstream_gene_variant | MODIFIER | c.*2419C>T| |
S215 |
9 | BAA01g17880 | A01 | 8709423 | G | A | downstream_gene_variant | MODIFIER | c.*3414G>A| |
S284 |