Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34450 | A02 | 29546553 | C | T | missense_variant | MODERATE | c.385G>A|p.Gly129Ser |
S152 |
2 | BAA02g34450 | A02 | 29547148 | C | T | upstream_gene_variant | MODIFIER | c.-9G>A| |
S139 S32 |
3 | BAA02g34450 | A02 | 29547319 | C | T | upstream_gene_variant | MODIFIER | c.-180G>A| |
S167 |
4 | BAA02g34450 | A02 | 29547351 | C | T | upstream_gene_variant | MODIFIER | c.-212G>A| |
S208 |
5 | BAA02g34450 | A02 | 29547718 | C | T | upstream_gene_variant | MODIFIER | c.-579G>A| |
S135 |
6 | BAA02g34450 | A02 | 29548267 | G | A | upstream_gene_variant | MODIFIER | c.-1128C>T| |
S265 |
7 | BAA02g34450 | A02 | 29548737 | G | A | upstream_gene_variant | MODIFIER | c.-1598C>T| |
S136 |
8 | BAA02g34450 | A02 | 29550795 | C | T | upstream_gene_variant | MODIFIER | c.-3656G>A| |
S177 |
9 | BAA02g34450 | A02 | 29551487 | G | A | upstream_gene_variant | MODIFIER | c.-4348C>T| |
S225 S73 |