Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g22740 | A08 | 16999580 | G | A | upstream_gene_variant | MODIFIER | c.-3892G>A| |
S281 |
2 | BAA08g22740 | A08 | 16999972 | C | T | upstream_gene_variant | MODIFIER | c.-3500C>T| |
S53 |
3 | BAA08g22740 | A08 | 17001415 | G | A | upstream_gene_variant | MODIFIER | c.-2057G>A| |
S72 S78 |
4 | BAA08g22740 | A08 | 17002545 | G | A | upstream_gene_variant | MODIFIER | c.-927G>A| |
S127 |
5 | BAA08g22740 | A08 | 17002971 | G | A | upstream_gene_variant | MODIFIER | c.-501G>A| |
S41 |
6 | BAA08g22740 | A08 | 17004155 | C | T | intron_variant | MODIFIER | c.323-40C>T| |
S157 S163 |
7 | BAA08g22740 | A08 | 17004606 | C | T | synonymous_variant | LOW | c.498C>T|p.Phe166Phe |
S186 |
8 | BAA08g22740 | A08 | 17004782 | G | A | missense_variant | MODERATE | c.589G>A|p.Gly197Ser |
S241 |
9 | BAA08g22740 | A08 | 17006385 | C | T | downstream_gene_variant | MODIFIER | c.*393C>T| |
S175 |
10 | BAA08g22740 | A08 | 17006929 | G | A | downstream_gene_variant | MODIFIER | c.*937G>A| |
S298 |
11 | BAA08g22740 | A08 | 17007146 | C | T | downstream_gene_variant | MODIFIER | c.*1154C>T| |
S293 |
12 | BAA08g22740 | A08 | 17007622 | C | T | downstream_gene_variant | MODIFIER | c.*1630C>T| |
S303 |