Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g11190 | A02 | 5059666 | C | T | missense_variant | MODERATE | c.733G>A|p.Gly245Ser |
S178 |
2 | BAA02g11190 | A02 | 5059790 | C | T | synonymous_variant | LOW | c.609G>A|p.Glu203Glu |
S255 |
3 | BAA02g11190 | A02 | 5059920 | G | A | missense_variant | MODERATE | c.479C>T|p.Pro160Leu |
S136 |
4 | BAA02g11190 | A02 | 5060175 | G | A | missense_variant | MODERATE | c.311C>T|p.Thr104Ile |
S289 S290 |
5 | BAA02g11190 | A02 | 5060521 | G | A | upstream_gene_variant | MODIFIER | c.-36C>T| |
S125 |
6 | BAA02g11190 | A02 | 5064319 | G | A | upstream_gene_variant | MODIFIER | c.-3834C>T| |
S276 |
7 | BAA02g11190 | A02 | 5065395 | G | A | upstream_gene_variant | MODIFIER | c.-4910C>T| |
S288 |