Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g30060 | A04 | 28809288 | G | A | upstream_gene_variant | MODIFIER | c.-3259G>A| |
S18 |
2 | BAA04g30060 | A04 | 28809600 | G | A | upstream_gene_variant | MODIFIER | c.-2947G>A| |
S52 |
3 | BAA04g30060 | A04 | 28810834 | G | A | upstream_gene_variant | MODIFIER | c.-1713G>A| |
S163 |
4 | BAA04g30060 | A04 | 28811097 | G | A | upstream_gene_variant | MODIFIER | c.-1450G>A| |
S71 |
5 | BAA04g30060 | A04 | 28811206 | G | A | upstream_gene_variant | MODIFIER | c.-1341G>A| |
S139 |
6 | BAA04g30060 | A04 | 28812058 | C | T | upstream_gene_variant | MODIFIER | c.-489C>T| |
S244 |
7 | BAA04g30060 | A04 | 28812307 | G | A | upstream_gene_variant | MODIFIER | c.-240G>A| |
S261 |
8 | BAA04g30060 | A04 | 28812856 | G | A | intron_variant | MODIFIER | c.264+46G>A| |
S282 |
9 | BAA04g30060 | A04 | 28813024 | G | A | intron_variant | MODIFIER | c.264+214G>A| |
S264 |
10 | BAA04g30060 | A04 | 28813185 | C | T | intron_variant | MODIFIER | c.265-256C>T| |
S80 |
11 | BAA04g30060 | A04 | 28813502 | C | T | missense_variant | MODERATE | c.326C>T|p.Ser109Leu |
S283 |
12 | BAA04g30060 | A04 | 28813563 | T | G | missense_variant | MODERATE | c.387T>G|p.Asn129Lys |
S23 |
13 | BAA04g30060 | A04 | 28814100 | G | A | intron_variant | MODIFIER | c.788+136G>A| |
S282 |
14 | BAA04g30060 | A04 | 28814319 | G | A | intron_variant | MODIFIER | c.788+355G>A| |
S274 |
15 | BAA04g30060 | A04 | 28814335 | C | T | intron_variant | MODIFIER | c.788+371C>T| |
S234 |
16 | BAA04g30060 | A04 | 28814398 | T | C | intron_variant | MODIFIER | c.788+434T>C| |
S76 |
17 | BAA04g30060 | A04 | 28814565 | C | T | intron_variant | MODIFIER | c.788+601C>T| |
S308 |
18 | BAA04g30060 | A04 | 28814655 | G | A | intron_variant | MODIFIER | c.788+691G>A| |
S294 |
19 | BAA04g30060 | A04 | 28815031 | C | T | intron_variant | MODIFIER | c.788+1067C>T| |
S64 |
20 | BAA04g30060 | A04 | 28815234 | G | A | intron_variant | MODIFIER | c.788+1270G>A| |
S66 S98 |
21 | BAA04g30060 | A04 | 28815836 | G | A | intron_variant | MODIFIER | c.789-984G>A| |
S111 |
22 | BAA04g30060 | A04 | 28816056 | G | A | intron_variant | MODIFIER | c.789-764G>A| |
S199 |
23 | BAA04g30060 | A04 | 28816272 | G | A | intron_variant | MODIFIER | c.789-548G>A| |
S289 S290 |
24 | BAA04g30060 | A04 | 28816290 | G | A | intron_variant | MODIFIER | c.789-530G>A| |
S36 |
25 | BAA04g30060 | A04 | 28816417 | G | A | intron_variant | MODIFIER | c.789-403G>A| |
S150 |