Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19080 | A02 | 9887107 | C | T | synonymous_variant | LOW | c.453G>A|p.Leu151Leu |
S166 |
2 | BAA02g19080 | A02 | 9887504 | G | A | missense_variant | MODERATE | c.56C>T|p.Ser19Phe |
S162 |
3 | BAA02g19080 | A02 | 9889499 | C | T | upstream_gene_variant | MODIFIER | c.-1940G>A| |
S186 |
4 | BAA02g19080 | A02 | 9889599 | G | A | upstream_gene_variant | MODIFIER | c.-2040C>T| |
S215 S36 |
5 | BAA02g19080 | A02 | 9890300 | G | A | upstream_gene_variant | MODIFIER | c.-2741C>T| |
S134 |
6 | BAA02g19080 | A02 | 9890553 | C | T | upstream_gene_variant | MODIFIER | c.-2994G>A| |
S155 S211 |
7 | BAA02g19080 | A02 | 9890811 | G | A | upstream_gene_variant | MODIFIER | c.-3252C>T| |
S11 |
8 | BAA02g19080 | A02 | 9892415 | C | T | upstream_gene_variant | MODIFIER | c.-4856G>A| |
S104 S52 |