Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g23640 | A01 | 12280209 | C | T | downstream_gene_variant | MODIFIER | c.*4872G>A| |
S44 |
2 | BAA01g23640 | A01 | 12280690 | C | T | downstream_gene_variant | MODIFIER | c.*4391G>A| |
S296 |
3 | BAA01g23640 | A01 | 12281055 | A | C | downstream_gene_variant | MODIFIER | c.*4026T>G| |
S130 S221 S252 S293 S294 |
4 | BAA01g23640 | A01 | 12281124 | G | A | downstream_gene_variant | MODIFIER | c.*3957C>T| |
S84 S93 |
5 | BAA01g23640 | A01 | 12281213 | C | T | downstream_gene_variant | MODIFIER | c.*3868G>A| |
S176 |
6 | BAA01g23640 | A01 | 12281642 | C | T | downstream_gene_variant | MODIFIER | c.*3439G>A| |
S159 S243 |
7 | BAA01g23640 | A01 | 12281771 | C | T | downstream_gene_variant | MODIFIER | c.*3310G>A| |
S130 |
8 | BAA01g23640 | A01 | 12282327 | G | A | downstream_gene_variant | MODIFIER | c.*2754C>T| |
S236 |
9 | BAA01g23640 | A01 | 12282389 | C | T | downstream_gene_variant | MODIFIER | c.*2692G>A| |
S25 |
10 | BAA01g23640 | A01 | 12282483 | G | A | downstream_gene_variant | MODIFIER | c.*2598C>T| |
S194 |
11 | BAA01g23640 | A01 | 12284710 | G | A | downstream_gene_variant | MODIFIER | c.*371C>T| |
S117 |
12 | BAA01g23640 | A01 | 12286050 | C | T | upstream_gene_variant | MODIFIER | c.-97G>A| |
S183 |
13 | BAA01g23640 | A01 | 12286531 | C | T | upstream_gene_variant | MODIFIER | c.-578G>A| |
S16 S272 |
14 | BAA01g23640 | A01 | 12287106 | C | T | upstream_gene_variant | MODIFIER | c.-1153G>A| |
S198 |
15 | BAA01g23640 | A01 | 12289574 | G | A | upstream_gene_variant | MODIFIER | c.-3621C>T| |
S293 |
16 | BAA01g23640 | A01 | 12289611 | C | T | upstream_gene_variant | MODIFIER | c.-3658G>A| |
S128 |
17 | BAA01g23640 | A01 | 12289948 | G | A | upstream_gene_variant | MODIFIER | c.-3995C>T| |
S202 |
18 | BAA01g23640 | A01 | 12290045 | G | A | upstream_gene_variant | MODIFIER | c.-4092C>T| |
S159 S243 S276 S298 S299 |
19 | BAA01g23640 | A01 | 12290065 | C | T | upstream_gene_variant | MODIFIER | c.-4112G>A| |
S164 |