Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA06g18660 | A06 | 9542277 | G | A | missense_variant | MODERATE | c.4G>A|p.Gly2Ser |
S236 |
2 | BAA06g18660 | A06 | 9544608 | G | A | downstream_gene_variant | MODIFIER | c.*1903G>A| |
S182 |
3 | BAA06g18660 | A06 | 9545199 | C | T | downstream_gene_variant | MODIFIER | c.*2494C>T| |
S165 |
4 | BAA06g18660 | A06 | 9545476 | C | T | downstream_gene_variant | MODIFIER | c.*2771C>T| |
S11 |
5 | BAA06g18660 | A06 | 9545901 | G | A | downstream_gene_variant | MODIFIER | c.*3196G>A| |
S256 |
6 | BAA06g18660 | A06 | 9547197 | C | T | downstream_gene_variant | MODIFIER | c.*4492C>T| |
S184 |
7 | BAA06g18660 | A06 | 9547355 | G | A | downstream_gene_variant | MODIFIER | c.*4650G>A| |
S140 |