Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g22080 | A02 | 11889095 | G | A | upstream_gene_variant | MODIFIER | c.-24G>A| |
S247 |
2 | BAA02g22080 | A02 | 11889334 | G | A | synonymous_variant | LOW | c.216G>A|p.Thr72Thr |
S17 |
3 | BAA02g22080 | A02 | 11889412 | C | T | synonymous_variant | LOW | c.294C>T|p.Asp98Asp |
S123 |
4 | BAA02g22080 | A02 | 11889975 | G | A | missense_variant | MODERATE | c.649G>A|p.Ala217Thr |
S257 |
5 | BAA02g22080 | A02 | 11892427 | G | A | splice_region_variant&intron_variant | LOW | c.1719+5G>A| |
S298 |
6 | BAA02g22080 | A02 | 11892540 | G | A | synonymous_variant | LOW | c.1740G>A|p.Ala580Ala |
S212 |
7 | BAA02g22080 | A02 | 11892556 | C | T | synonymous_variant | LOW | c.1756C>T|p.Leu586Leu |
S242 |
8 | BAA02g22080 | A02 | 11894353 | G | A | downstream_gene_variant | MODIFIER | c.*768G>A| |
S70 |
9 | BAA02g22080 | A02 | 11895150 | C | T | downstream_gene_variant | MODIFIER | c.*1565C>T| |
S99 |
10 | BAA02g22080 | A02 | 11895245 | G | A | downstream_gene_variant | MODIFIER | c.*1660G>A| |
S59 |
11 | BAA02g22080 | A02 | 11896284 | C | T | downstream_gene_variant | MODIFIER | c.*2699C>T| |
S186 |
12 | BAA02g22080 | A02 | 11896676 | C | T | downstream_gene_variant | MODIFIER | c.*3091C>T| |
S157 S163 |
13 | BAA02g22080 | A02 | 11896712 | C | T | downstream_gene_variant | MODIFIER | c.*3127C>T| |
S20 |
14 | BAA02g22080 | A02 | 11897052 | G | A | downstream_gene_variant | MODIFIER | c.*3467G>A| |
S109 |
15 | BAA02g22080 | A02 | 11897151 | C | T | downstream_gene_variant | MODIFIER | c.*3566C>T| |
S270 |
16 | BAA02g22080 | A02 | 11897173 | C | T | downstream_gene_variant | MODIFIER | c.*3588C>T| |
S123 |
17 | BAA02g22080 | A02 | 11898023 | G | A | downstream_gene_variant | MODIFIER | c.*4438G>A| |
S111 |
18 | BAA02g22080 | A02 | 11898166 | C | T | downstream_gene_variant | MODIFIER | c.*4581C>T| |
S219 |
19 | BAA02g22080 | A02 | 11898255 | G | A | downstream_gene_variant | MODIFIER | c.*4670G>A| |
S150 |