Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35730 | A02 | 30781886 | G | A | missense_variant | MODERATE | c.442C>T|p.Pro148Ser |
S169 |
2 | BAA02g35730 | A02 | 30782088 | G | A | synonymous_variant | LOW | c.339C>T|p.Ala113Ala |
S13 S140 S168 S219 S279 S64 S72 |
3 | BAA02g35730 | A02 | 30782158 | C | T | missense_variant | MODERATE | c.269G>A|p.Gly90Glu |
S219 |
4 | BAA02g35730 | A02 | 30783529 | C | T | upstream_gene_variant | MODIFIER | c.-626G>A| |
S262 |
5 | BAA02g35730 | A02 | 30786032 | G | A | upstream_gene_variant | MODIFIER | c.-3129C>T| |
S61 |
6 | BAA02g35730 | A02 | 30786076 | C | T | upstream_gene_variant | MODIFIER | c.-3173G>A| |
S289 S290 |
7 | BAA02g35730 | A02 | 30787450 | C | T | upstream_gene_variant | MODIFIER | c.-4547G>A| |
S305 |