Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g19030 | A10 | 17602437 | C | T | upstream_gene_variant | MODIFIER | c.-4937C>T| |
S51 |
2 | BAA10g19030 | A10 | 17608621 | G | A | missense_variant | MODERATE | c.541G>A|p.Ala181Thr |
S193 |
3 | BAA10g19030 | A10 | 17610193 | G | A | downstream_gene_variant | MODIFIER | c.*832G>A| |
S192 |