Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42740 | A02 | 35587860 | C | T | synonymous_variant | LOW | c.768G>A|p.Glu256Glu |
S72 S78 |
2 | BAA02g42740 | A02 | 35587985 | C | T | missense_variant | MODERATE | c.643G>A|p.Ala215Thr |
S162 |
3 | BAA02g42740 | A02 | 35588094 | C | T | missense_variant | MODERATE | c.534G>A|p.Met178Ile |
S167 |
4 | BAA02g42740 | A02 | 35588102 | C | T | missense_variant | MODERATE | c.526G>A|p.Glu176Lys |
S195 |
5 | BAA02g42740 | A02 | 35588234 | G | A | missense_variant | MODERATE | c.394C>T|p.Leu132Phe |
S57 |
6 | BAA02g42740 | A02 | 35588596 | C | T | synonymous_variant | LOW | c.216G>A|p.Arg72Arg |
S76 |
7 | BAA02g42740 | A02 | 35588629 | G | A | synonymous_variant | LOW | c.183C>T|p.Asp61Asp |
S11 |
8 | BAA02g42740 | A02 | 35589072 | G | A | upstream_gene_variant | MODIFIER | c.-261C>T| |
S125 |
9 | BAA02g42740 | A02 | 35592232 | C | T | upstream_gene_variant | MODIFIER | c.-3421G>A| |
S95 |
10 | BAA02g42740 | A02 | 35592286 | C | T | upstream_gene_variant | MODIFIER | c.-3475G>A| |
S12 |
11 | BAA02g42740 | A02 | 35593184 | C | T | upstream_gene_variant | MODIFIER | c.-4373G>A| |
S80 |
12 | BAA02g42740 | A02 | 35593310 | C | T | upstream_gene_variant | MODIFIER | c.-4499G>A| |
S203 |