Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06150 | A02 | 2612636 | G | A | missense_variant | MODERATE | c.2197C>T|p.Leu733Phe |
S187 |
2 | BAA02g06150 | A02 | 2612858 | C | T | missense_variant | MODERATE | c.1975G>A|p.Glu659Lys |
S218 |
3 | BAA02g06150 | A02 | 2613741 | C | T | synonymous_variant | LOW | c.1092G>A|p.Arg364Arg |
S42 |
4 | BAA02g06150 | A02 | 2613935 | G | A | stop_gained | HIGH | c.898C>T|p.Gln300* |
S257 |
5 | BAA02g06150 | A02 | 2615234 | G | A | synonymous_variant | LOW | c.213C>T|p.Leu71Leu |
S291 |
6 | BAA02g06150 | A02 | 2615432 | G | A | synonymous_variant | LOW | c.15C>T|p.Ser5Ser |
S297 |
7 | BAA02g06150 | A02 | 2615743 | G | A | upstream_gene_variant | MODIFIER | c.-297C>T| |
S305 |
8 | BAA02g06150 | A02 | 2616141 | G | A | upstream_gene_variant | MODIFIER | c.-695C>T| |
S294 |
9 | BAA02g06150 | A02 | 2616509 | G | A | upstream_gene_variant | MODIFIER | c.-1063C>T| |
S203 |