Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00460 | A02 | 251659 | C | T | upstream_gene_variant | MODIFIER | c.-4986C>T| |
S178 |
2 | BAA02g00460 | A02 | 254777 | G | A | upstream_gene_variant | MODIFIER | c.-1868G>A| |
S125 |
3 | BAA02g00460 | A02 | 255220 | C | T | upstream_gene_variant | MODIFIER | c.-1425C>T| |
S242 |
4 | BAA02g00460 | A02 | 255666 | C | T | upstream_gene_variant | MODIFIER | c.-979C>T| |
S99 |
5 | BAA02g00460 | A02 | 256629 | C | T | upstream_gene_variant | MODIFIER | c.-16C>T| |
S40 S49 |
6 | BAA02g00460 | A02 | 256761 | C | T | synonymous_variant | LOW | c.117C>T|p.His39His |
S133 |
7 | BAA02g00460 | A02 | 256935 | G | A | missense_variant | MODERATE | c.202G>A|p.Val68Met |
S125 |
8 | BAA02g00460 | A02 | 257954 | G | A | missense_variant | MODERATE | c.607G>A|p.Gly203Ser |
S279 |
9 | BAA02g00460 | A02 | 258143 | G | A | downstream_gene_variant | MODIFIER | c.*10G>A| |
S48 |