Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g45470 | A09 | 50665344 | C | T | downstream_gene_variant | MODIFIER | c.*1479G>A| |
S191 |
2 | BAA09g45470 | A09 | 50665855 | G | A | downstream_gene_variant | MODIFIER | c.*968C>T| |
S202 |
3 | BAA09g45470 | A09 | 50665956 | G | A | downstream_gene_variant | MODIFIER | c.*867C>T| |
S151 S263 |
4 | BAA09g45470 | A09 | 50666266 | C | T | downstream_gene_variant | MODIFIER | c.*557G>A| |
S95 |
5 | BAA09g45470 | A09 | 50666887 | C | T | stop_gained | HIGH | c.1280G>A|p.Trp427* |
S169 |
6 | BAA09g45470 | A09 | 50667158 | G | A | missense_variant | MODERATE | c.1097C>T|p.Thr366Ile |
S244 |
7 | BAA09g45470 | A09 | 50667503 | C | T | intron_variant | MODIFIER | c.874-46G>A| |
S179 |
8 | BAA09g45470 | A09 | 50669122 | G | A | synonymous_variant | LOW | c.354C>T|p.Ile118Ile |
S62 |
9 | BAA09g45470 | A09 | 50669219 | G | A | missense_variant | MODERATE | c.257C>T|p.Ser86Leu |
S274 |
10 | BAA09g45470 | A09 | 50669860 | C | T | synonymous_variant | LOW | c.126G>A|p.Arg42Arg |
S152 |
11 | BAA09g45470 | A09 | 50671170 | C | T | upstream_gene_variant | MODIFIER | c.-1185G>A| |
S67 |
12 | BAA09g45470 | A09 | 50672169 | C | T | upstream_gene_variant | MODIFIER | c.-2184G>A| |
S297 |
13 | BAA09g45470 | A09 | 50672873 | G | A | upstream_gene_variant | MODIFIER | c.-2888C>T| |
S79 S91 |
14 | BAA09g45470 | A09 | 50673013 | G | A | upstream_gene_variant | MODIFIER | c.-3028C>T| |
S264 |
15 | BAA09g45470 | A09 | 50673701 | G | A | upstream_gene_variant | MODIFIER | c.-3716C>T| |
S23 |
16 | BAA09g45470 | A09 | 50674350 | G | A | upstream_gene_variant | MODIFIER | c.-4365C>T| |
S207 |
17 | BAA09g45470 | A09 | 50674447 | C | T | upstream_gene_variant | MODIFIER | c.-4462G>A| |
S96 |