Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13470 | A02 | 6197714 | C | T | missense_variant | MODERATE | c.1379G>A|p.Arg460Gln |
S153 |
2 | BAA02g13470 | A02 | 6198172 | C | T | synonymous_variant | LOW | c.921G>A|p.Gln307Gln |
S116 |
3 | BAA02g13470 | A02 | 6198444 | G | A | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S190 |
4 | BAA02g13470 | A02 | 6198449 | G | A | missense_variant | MODERATE | c.644C>T|p.Ser215Phe |
S23 |
5 | BAA02g13470 | A02 | 6198648 | G | A | missense_variant | MODERATE | c.445C>T|p.Pro149Ser |
S228 |
6 | BAA02g13470 | A02 | 6198703 | C | T | synonymous_variant | LOW | c.390G>A|p.Leu130Leu |
S177 |
7 | BAA02g13470 | A02 | 6198762 | C | T | missense_variant | MODERATE | c.331G>A|p.Gly111Arg |
S201 |
8 | BAA02g13470 | A02 | 6201146 | G | A | upstream_gene_variant | MODIFIER | c.-2054C>T| |
S295 |
9 | BAA02g13470 | A02 | 6201360 | G | A | upstream_gene_variant | MODIFIER | c.-2268C>T| |
S146 |
10 | BAA02g13470 | A02 | 6203258 | C | T | upstream_gene_variant | MODIFIER | c.-4166G>A| |
S266 |