Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g15460 | A02 | 7458598 | C | T | downstream_gene_variant | MODIFIER | c.*2547G>A| |
S49 |
2 | BAA02g15460 | A02 | 7458915 | G | A | downstream_gene_variant | MODIFIER | c.*2230C>T| |
S206 |
3 | BAA02g15460 | A02 | 7459140 | C | T | downstream_gene_variant | MODIFIER | c.*2005G>A| |
S87 |
4 | BAA02g15460 | A02 | 7459574 | G | A | downstream_gene_variant | MODIFIER | c.*1571C>T| |
S190 |
5 | BAA02g15460 | A02 | 7459779 | C | T | downstream_gene_variant | MODIFIER | c.*1366G>A| |
S66 |
6 | BAA02g15460 | A02 | 7459806 | G | A | downstream_gene_variant | MODIFIER | c.*1339C>T| |
S11 |
7 | BAA02g15460 | A02 | 7460302 | C | T | downstream_gene_variant | MODIFIER | c.*843G>A| |
S234 |
8 | BAA02g15460 | A02 | 7460967 | C | T | downstream_gene_variant | MODIFIER | c.*178G>A| |
S46 |
9 | BAA02g15460 | A02 | 7461881 | C | T | missense_variant | MODERATE | c.446G>A|p.Gly149Asp |
S206 S26 |
10 | BAA02g15460 | A02 | 7463083 | G | A | upstream_gene_variant | MODIFIER | c.-679C>T| |
S96 |
11 | BAA02g15460 | A02 | 7463509 | C | T | upstream_gene_variant | MODIFIER | c.-1105G>A| |
S15 S2 S3 S34 S4 S6 |
12 | BAA02g15460 | A02 | 7463674 | G | A | upstream_gene_variant | MODIFIER | c.-1270C>T| |
S287 |
13 | BAA02g15460 | A02 | 7463782 | G | A | upstream_gene_variant | MODIFIER | c.-1378C>T| |
S133 |
14 | BAA02g15460 | A02 | 7463845 | G | A | upstream_gene_variant | MODIFIER | c.-1441C>T| |
S61 |
15 | BAA02g15460 | A02 | 7464856 | G | A | upstream_gene_variant | MODIFIER | c.-2452C>T| |
S209 |
16 | BAA02g15460 | A02 | 7465018 | C | T | upstream_gene_variant | MODIFIER | c.-2614G>A| |
S165 |
17 | BAA02g15460 | A02 | 7465382 | G | A | upstream_gene_variant | MODIFIER | c.-2978C>T| |
S176 |