Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g09530 | A08 | 8697725 | A | G | downstream_gene_variant | MODIFIER | c.*2819T>C| |
S274 |
2 | BAA08g09530 | A08 | 8700930 | G | A | missense_variant | MODERATE | c.1444C>T|p.Arg482Trp |
S187 |
3 | BAA08g09530 | A08 | 8701645 | G | T | synonymous_variant | LOW | c.729C>A|p.Gly243Gly |
S297 |
4 | BAA08g09530 | A08 | 8701809 | C | T | missense_variant | MODERATE | c.565G>A|p.Glu189Lys |
S284 |
5 | BAA08g09530 | A08 | 8701852 | C | T | synonymous_variant | LOW | c.522G>A|p.Leu174Leu |
S168 |
6 | BAA08g09530 | A08 | 8701859 | G | A | missense_variant | MODERATE | c.515C>T|p.Thr172Ile |
S260 |
7 | BAA08g09530 | A08 | 8702148 | G | A | missense_variant | MODERATE | c.226C>T|p.Leu76Phe |
S68 |
8 | BAA08g09530 | A08 | 8702228 | C | T | missense_variant | MODERATE | c.146G>A|p.Gly49Glu |
S252 |
9 | BAA08g09530 | A08 | 8706591 | G | A | upstream_gene_variant | MODIFIER | c.-4218C>T| |
S117 |