Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g10980 | A05 | 5588567 | G | A | upstream_gene_variant | MODIFIER | c.-4690G>A| |
S286 |
2 | BAA05g10980 | A05 | 5590464 | C | T | upstream_gene_variant | MODIFIER | c.-2793C>T| |
S54 |
3 | BAA05g10980 | A05 | 5590703 | G | A | upstream_gene_variant | MODIFIER | c.-2554G>A| |
S15 S3 |
4 | BAA05g10980 | A05 | 5590765 | C | T | upstream_gene_variant | MODIFIER | c.-2492C>T| |
S167 |
5 | BAA05g10980 | A05 | 5590844 | G | A | upstream_gene_variant | MODIFIER | c.-2413G>A| |
S192 |
6 | BAA05g10980 | A05 | 5591139 | C | T | upstream_gene_variant | MODIFIER | c.-2118C>T| |
S292 |
7 | BAA05g10980 | A05 | 5591435 | G | A | upstream_gene_variant | MODIFIER | c.-1822G>A| |
S190 |
8 | BAA05g10980 | A05 | 5592394 | C | T | upstream_gene_variant | MODIFIER | c.-863C>T| |
S100 |
9 | BAA05g10980 | A05 | 5592736 | C | T | upstream_gene_variant | MODIFIER | c.-521C>T| |
S197 |
10 | BAA05g10980 | A05 | 5592766 | C | T | upstream_gene_variant | MODIFIER | c.-491C>T| |
S186 |
11 | BAA05g10980 | A05 | 5593745 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.196-1G>A| |
S240 |
12 | BAA05g10980 | A05 | 5594094 | C | T | downstream_gene_variant | MODIFIER | c.*7C>T| |
S197 |
13 | BAA05g10980 | A05 | 5594121 | C | T | downstream_gene_variant | MODIFIER | c.*34C>T| |
S247 |
14 | BAA05g10980 | A05 | 5594191 | C | T | downstream_gene_variant | MODIFIER | c.*104C>T| |
S261 |
15 | BAA05g10980 | A05 | 5594251 | G | A | downstream_gene_variant | MODIFIER | c.*164G>A| |
S153 |