Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04850 | A02 | 2110986 | G | A | stop_gained | HIGH | c.154C>T|p.Gln52* |
S128 |
2 | BAA02g04850 | A02 | 2111247 | G | A | upstream_gene_variant | MODIFIER | c.-108C>T| |
S246 |
3 | BAA02g04850 | A02 | 2111273 | A | G | upstream_gene_variant | MODIFIER | c.-134T>C| |
S221 |
4 | BAA02g04850 | A02 | 2111530 | C | T | upstream_gene_variant | MODIFIER | c.-391G>A| |
S18 |
5 | BAA02g04850 | A02 | 2111767 | G | A | upstream_gene_variant | MODIFIER | c.-628C>T| |
S52 |
6 | BAA02g04850 | A02 | 2111963 | G | A | upstream_gene_variant | MODIFIER | c.-824C>T| |
S293 |
7 | BAA02g04850 | A02 | 2112316 | A | G | upstream_gene_variant | MODIFIER | c.-1177T>C| |
S81 S85 |
8 | BAA02g04850 | A02 | 2112630 | G | A | upstream_gene_variant | MODIFIER | c.-1491C>T| |
S67 |
9 | BAA02g04850 | A02 | 2112790 | C | T | upstream_gene_variant | MODIFIER | c.-1651G>A| |
S99 |
10 | BAA02g04850 | A02 | 2113006 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S82 S92 |
11 | BAA02g04850 | A02 | 2113751 | C | T | upstream_gene_variant | MODIFIER | c.-2612G>A| |
S278 |
12 | BAA02g04850 | A02 | 2114506 | G | A | upstream_gene_variant | MODIFIER | c.-3367C>T| |
S90 |
13 | BAA02g04850 | A02 | 2116101 | C | T | upstream_gene_variant | MODIFIER | c.-4962G>A| |
S15 S3 |