Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10980 | A02 | 4938376 | G | A | upstream_gene_variant | MODIFIER | c.-2346G>A| |
S91 |
2 | BAA02g10980 | A02 | 4939744 | G | A | upstream_gene_variant | MODIFIER | c.-978G>A| |
S107 |
3 | BAA02g10980 | A02 | 4940101 | C | T | upstream_gene_variant | MODIFIER | c.-621C>T| |
S251 |
4 | BAA02g10980 | A02 | 4940302 | G | A | upstream_gene_variant | MODIFIER | c.-420G>A| |
S159 S243 |
5 | BAA02g10980 | A02 | 4940323 | C | T | upstream_gene_variant | MODIFIER | c.-399C>T| |
S34 |
6 | BAA02g10980 | A02 | 4940570 | G | A | upstream_gene_variant | MODIFIER | c.-152G>A| |
S247 |
7 | BAA02g10980 | A02 | 4941089 | C | T | missense_variant | MODERATE | c.340C>T|p.Pro114Ser |
S292 |
8 | BAA02g10980 | A02 | 4941963 | C | T | missense_variant | MODERATE | c.914C>T|p.Ser305Leu |
S209 |
9 | BAA02g10980 | A02 | 4942229 | G | A | synonymous_variant | LOW | c.1071G>A|p.Gly357Gly |
S246 |