Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27850 | A02 | 15689099 | G | A | splice_region_variant&intron_variant | LOW | c.993+7C>T| |
S292 |
2 | BAA02g27850 | A02 | 15689899 | C | T | missense_variant | MODERATE | c.560G>A|p.Arg187Lys |
S88 |
3 | BAA02g27850 | A02 | 15690472 | G | A | synonymous_variant | LOW | c.237C>T|p.Phe79Phe |
S295 |
4 | BAA02g27850 | A02 | 15694878 | C | T | upstream_gene_variant | MODIFIER | c.-4099G>A| |
S237 |
5 | BAA02g27850 | A02 | 15695131 | C | T | upstream_gene_variant | MODIFIER | c.-4352G>A| |
S271 S289 S290 S299 |
6 | BAA02g27850 | A02 | 15695204 | C | T | upstream_gene_variant | MODIFIER | c.-4425G>A| |
S38 |