Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46160 | A09 | 51049449 | C | T | missense_variant | MODERATE | c.137G>A|p.Gly46Asp |
S303 |
2 | BAA09g46160 | A09 | 51049979 | C | T | upstream_gene_variant | MODIFIER | c.-394G>A| |
S219 S72 |
3 | BAA09g46160 | A09 | 51050346 | G | A | upstream_gene_variant | MODIFIER | c.-761C>T| |
S185 |
4 | BAA09g46160 | A09 | 51050640 | G | A | upstream_gene_variant | MODIFIER | c.-1055C>T| |
S38 |
5 | BAA09g46160 | A09 | 51051224 | C | T | upstream_gene_variant | MODIFIER | c.-1639G>A| |
S164 |
6 | BAA09g46160 | A09 | 51051863 | G | A | upstream_gene_variant | MODIFIER | c.-2278C>T| |
S291 |
7 | BAA09g46160 | A09 | 51053737 | C | T | upstream_gene_variant | MODIFIER | c.-4152G>A| |
S186 |
8 | BAA09g46160 | A09 | 51054283 | C | T | upstream_gene_variant | MODIFIER | c.-4698G>A| |
S125 |