Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18140 | A02 | 9133363 | C | T | upstream_gene_variant | MODIFIER | c.-4311C>T| |
S308 |
2 | BAA02g18140 | A02 | 9133730 | C | T | upstream_gene_variant | MODIFIER | c.-3944C>T| |
S209 |
3 | BAA02g18140 | A02 | 9134970 | C | T | upstream_gene_variant | MODIFIER | c.-2704C>T| |
S105 S106 |
4 | BAA02g18140 | A02 | 9135095 | G | A | upstream_gene_variant | MODIFIER | c.-2579G>A| |
S293 |
5 | BAA02g18140 | A02 | 9137738 | C | T | missense_variant | MODERATE | c.65C>T|p.Ser22Phe |
S171 |
6 | BAA02g18140 | A02 | 9137959 | G | A | intron_variant | MODIFIER | c.82+204G>A| |
S10 |
7 | BAA02g18140 | A02 | 9138483 | G | A | synonymous_variant | LOW | c.264G>A|p.Gln88Gln |
S17 |
8 | BAA02g18140 | A02 | 9138801 | G | A | synonymous_variant | LOW | c.582G>A|p.Gln194Gln |
S282 |
9 | BAA02g18140 | A02 | 9140711 | G | A | downstream_gene_variant | MODIFIER | c.*676G>A| |
S146 |
10 | BAA02g18140 | A02 | 9140877 | G | A | downstream_gene_variant | MODIFIER | c.*842G>A| |
S37 |
11 | BAA02g18140 | A02 | 9141081 | G | A | downstream_gene_variant | MODIFIER | c.*1046G>A| |
S82 S92 |
12 | BAA02g18140 | A02 | 9141637 | C | T | downstream_gene_variant | MODIFIER | c.*1602C>T| |
S176 |
13 | BAA02g18140 | A02 | 9144809 | C | T | downstream_gene_variant | MODIFIER | c.*4774C>T| |
S218 |