Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g46570 | A02 | 37825770 | G | A | upstream_gene_variant | MODIFIER | c.-4634G>A| |
S292 |
2 | BAA02g46570 | A02 | 37826017 | G | A | upstream_gene_variant | MODIFIER | c.-4387G>A| |
S71 |
3 | BAA02g46570 | A02 | 37827118 | G | A | upstream_gene_variant | MODIFIER | c.-3286G>A| |
S81 S85 |
4 | BAA02g46570 | A02 | 37827721 | G | A | upstream_gene_variant | MODIFIER | c.-2683G>A| |
S2 |
5 | BAA02g46570 | A02 | 37828879 | G | A | upstream_gene_variant | MODIFIER | c.-1525G>A| |
S234 |
6 | BAA02g46570 | A02 | 37829346 | G | A | upstream_gene_variant | MODIFIER | c.-1058G>A| |
S13 |
7 | BAA02g46570 | A02 | 37829499 | G | A | upstream_gene_variant | MODIFIER | c.-905G>A| |
S155 |
8 | BAA02g46570 | A02 | 37829959 | G | T | upstream_gene_variant | MODIFIER | c.-445G>T| |
S117 S130 S139 S14 S140 S146 S179 S219 S245 S267 S294 S303 S64 S88 S92 |
9 | BAA02g46570 | A02 | 37830419 | C | T | missense_variant | MODERATE | c.16C>T|p.Pro6Ser |
S237 |
10 | BAA02g46570 | A02 | 37831063 | G | A | missense_variant&splice_region_variant | MODERATE | c.390G>A|p.Met130Ile |
S30 |
11 | BAA02g46570 | A02 | 37832120 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S100 |