Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44080 | A02 | 36386919 | G | A | upstream_gene_variant | MODIFIER | c.-4591G>A| |
S113 |
2 | BAA02g44080 | A02 | 36389895 | C | T | upstream_gene_variant | MODIFIER | c.-1615C>T| |
S85 |
3 | BAA02g44080 | A02 | 36391701 | G | A | missense_variant | MODERATE | c.100G>A|p.Ala34Thr |
S103 S136 |
4 | BAA02g44080 | A02 | 36393703 | C | T | synonymous_variant | LOW | c.754C>T|p.Leu252Leu |
S15 |
5 | BAA02g44080 | A02 | 36394129 | G | A | missense_variant | MODERATE | c.1096G>A|p.Ala366Thr |
S259 |
6 | BAA02g44080 | A02 | 36394928 | G | A | missense_variant | MODERATE | c.1390G>A|p.Ala464Thr |
S134 |
7 | BAA02g44080 | A02 | 36395171 | G | A | missense_variant | MODERATE | c.1505G>A|p.Arg502Lys |
S229 |