Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g37770 | A02 | 32288997 | C | T | upstream_gene_variant | MODIFIER | c.-3757C>T| |
S40 S49 |
2 | BAA02g37770 | A02 | 32289220 | G | A | upstream_gene_variant | MODIFIER | c.-3534G>A| |
S223 |
3 | BAA02g37770 | A02 | 32289493 | G | A | upstream_gene_variant | MODIFIER | c.-3261G>A| |
S60 |
4 | BAA02g37770 | A02 | 32289707 | G | A | upstream_gene_variant | MODIFIER | c.-3047G>A| |
S169 |
5 | BAA02g37770 | A02 | 32289785 | G | A | upstream_gene_variant | MODIFIER | c.-2969G>A| |
S86 |
6 | BAA02g37770 | A02 | 32289899 | C | T | upstream_gene_variant | MODIFIER | c.-2855C>T| |
S182 |
7 | BAA02g37770 | A02 | 32290901 | G | A | upstream_gene_variant | MODIFIER | c.-1853G>A| |
S37 |
8 | BAA02g37770 | A02 | 32291129 | G | A | upstream_gene_variant | MODIFIER | c.-1625G>A| |
S256 |
9 | BAA02g37770 | A02 | 32291215 | G | A | upstream_gene_variant | MODIFIER | c.-1539G>A| |
S155 S211 S90 |
10 | BAA02g37770 | A02 | 32293141 | C | T | missense_variant | MODERATE | c.388C>T|p.Pro130Ser |
S61 |
11 | BAA02g37770 | A02 | 32293696 | G | A | missense_variant | MODERATE | c.943G>A|p.Ala315Thr |
S20 |
12 | BAA02g37770 | A02 | 32294524 | C | T | stop_gained | HIGH | c.1771C>T|p.Gln591* |
S180 |
13 | BAA02g37770 | A02 | 32297905 | C | T | downstream_gene_variant | MODIFIER | c.*3328C>T| |
S128 |
14 | BAA02g37770 | A02 | 32297922 | G | A | downstream_gene_variant | MODIFIER | c.*3345G>A| |
S25 |
15 | BAA02g37770 | A02 | 32298038 | C | T | downstream_gene_variant | MODIFIER | c.*3461C>T| |
S138 |
16 | BAA02g37770 | A02 | 32298643 | G | A | downstream_gene_variant | MODIFIER | c.*4066G>A| |
S56 |
17 | BAA02g37770 | A02 | 32298654 | C | T | downstream_gene_variant | MODIFIER | c.*4077C>T| |
S112 |
18 | BAA02g37770 | A02 | 32298829 | C | T | downstream_gene_variant | MODIFIER | c.*4252C>T| |
S9 |