Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35560 | A02 | 30562618 | C | T | downstream_gene_variant | MODIFIER | c.*4751G>A| |
S203 |
2 | BAA02g35560 | A02 | 30563165 | C | T | downstream_gene_variant | MODIFIER | c.*4204G>A| |
S116 |
3 | BAA02g35560 | A02 | 30563453 | C | T | downstream_gene_variant | MODIFIER | c.*3916G>A| |
S138 |
4 | BAA02g35560 | A02 | 30563712 | A | T | downstream_gene_variant | MODIFIER | c.*3657T>A| |
S232 |
5 | BAA02g35560 | A02 | 30564314 | C | T | downstream_gene_variant | MODIFIER | c.*3055G>A| |
S221 |
6 | BAA02g35560 | A02 | 30565790 | G | A | downstream_gene_variant | MODIFIER | c.*1579C>T| |
S293 |
7 | BAA02g35560 | A02 | 30568263 | C | T | intron_variant | MODIFIER | c.1144+247G>A| |
S23 |
8 | BAA02g35560 | A02 | 30568722 | G | A | intron_variant | MODIFIER | c.1095+60C>T| |
S256 |
9 | BAA02g35560 | A02 | 30569327 | C | T | intron_variant | MODIFIER | c.835+12G>A| |
S263 |
10 | BAA02g35560 | A02 | 30569664 | C | T | synonymous_variant | LOW | c.510G>A|p.Arg170Arg |
S177 |
11 | BAA02g35560 | A02 | 30570742 | C | T | upstream_gene_variant | MODIFIER | c.-569G>A| |
S203 |
12 | BAA02g35560 | A02 | 30571088 | G | A | upstream_gene_variant | MODIFIER | c.-915C>T| |
S38 |
13 | BAA02g35560 | A02 | 30571131 | C | T | upstream_gene_variant | MODIFIER | c.-958G>A| |
S6 |
14 | BAA02g35560 | A02 | 30572306 | C | T | upstream_gene_variant | MODIFIER | c.-2133G>A| |
S276 |
15 | BAA02g35560 | A02 | 30573468 | C | T | upstream_gene_variant | MODIFIER | c.-3295G>A| |
S308 |
16 | BAA02g35560 | A02 | 30574160 | C | T | upstream_gene_variant | MODIFIER | c.-3987G>A| |
S182 |
17 | BAA02g35560 | A02 | 30574165 | G | A | upstream_gene_variant | MODIFIER | c.-3992C>T| |
S293 |