Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21700 | A01 | 10786418 | G | A | downstream_gene_variant | MODIFIER | c.*3942C>T| |
S280 |
2 | BAA01g21700 | A01 | 10786569 | G | A | downstream_gene_variant | MODIFIER | c.*3791C>T| |
S116 |
3 | BAA01g21700 | A01 | 10786634 | G | A | downstream_gene_variant | MODIFIER | c.*3726C>T| |
S237 |
4 | BAA01g21700 | A01 | 10787767 | C | T | downstream_gene_variant | MODIFIER | c.*2593G>A| |
S148 S210 S30 S31 |
5 | BAA01g21700 | A01 | 10789602 | C | T | downstream_gene_variant | MODIFIER | c.*758G>A| |
S264 |
6 | BAA01g21700 | A01 | 10789818 | C | T | downstream_gene_variant | MODIFIER | c.*542G>A| |
S255 |
7 | BAA01g21700 | A01 | 10790475 | C | T | missense_variant | MODERATE | c.206G>A|p.Gly69Glu |
S63 |
8 | BAA01g21700 | A01 | 10790720 | C | T | synonymous_variant | LOW | c.27G>A|p.Glu9Glu |
S210 S225 |
9 | BAA01g21700 | A01 | 10792613 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S268 |
10 | BAA01g21700 | A01 | 10793615 | C | T | upstream_gene_variant | MODIFIER | c.-2869G>A| |
S135 |
11 | BAA01g21700 | A01 | 10794056 | C | T | upstream_gene_variant | MODIFIER | c.-3310G>A| |
S41 |
12 | BAA01g21700 | A01 | 10794163 | C | T | upstream_gene_variant | MODIFIER | c.-3417G>A| |
S65 |
13 | BAA01g21700 | A01 | 10794760 | G | A | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S193 |