Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g01660 | A01 | 733735 | G | A | missense_variant | MODERATE | c.1084C>T|p.Pro362Ser |
S276 |
2 | BAA01g01660 | A01 | 734235 | G | A | missense_variant | MODERATE | c.763C>T|p.Arg255Cys |
S251 |
3 | BAA01g01660 | A01 | 734283 | C | T | missense_variant | MODERATE | c.715G>A|p.Glu239Lys |
S185 |
4 | BAA01g01660 | A01 | 734339 | C | T | missense_variant | MODERATE | c.659G>A|p.Gly220Asp |
S148 S30 S31 |
5 | BAA01g01660 | A01 | 734350 | G | A | synonymous_variant | LOW | c.648C>T|p.Ala216Ala |
S191 |
6 | BAA01g01660 | A01 | 734589 | G | A | missense_variant | MODERATE | c.409C>T|p.Leu137Phe |
S56 |
7 | BAA01g01660 | A01 | 737155 | G | A | upstream_gene_variant | MODIFIER | c.-2158C>T| |
S234 |
8 | BAA01g01660 | A01 | 737471 | G | A | upstream_gene_variant | MODIFIER | c.-2474C>T| |
S256 |