Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g03650 | A09 | 2186503 | G | A | downstream_gene_variant | MODIFIER | c.*1093C>T| |
S281 |
2 | BAA09g03650 | A09 | 2186851 | G | A | downstream_gene_variant | MODIFIER | c.*745C>T| |
S152 |
3 | BAA09g03650 | A09 | 2187416 | C | T | downstream_gene_variant | MODIFIER | c.*180G>A| |
S52 |
4 | BAA09g03650 | A09 | 2187589 | C | T | downstream_gene_variant | MODIFIER | c.*7G>A| |
S39 |
5 | BAA09g03650 | A09 | 2188111 | G | A | missense_variant | MODERATE | c.3181C>T|p.Arg1061Cys |
S259 |
6 | BAA09g03650 | A09 | 2188454 | C | T | synonymous_variant | LOW | c.2838G>A|p.Thr946Thr |
S256 |
7 | BAA09g03650 | A09 | 2188734 | G | A | missense_variant | MODERATE | c.2558C>T|p.Ser853Phe |
S166 |
8 | BAA09g03650 | A09 | 2190955 | A | T | intron_variant | MODIFIER | c.1429-98T>A| |
S54 |
9 | BAA09g03650 | A09 | 2191324 | G | A | missense_variant | MODERATE | c.1216C>T|p.Leu406Phe |
S276 |
10 | BAA09g03650 | A09 | 2191835 | C | T | stop_gained | HIGH | c.804G>A|p.Trp268* |
S246 |
11 | BAA09g03650 | A09 | 2194176 | G | A | upstream_gene_variant | MODIFIER | c.-63C>T| |
S229 |
12 | BAA09g03650 | A09 | 2194920 | C | T | upstream_gene_variant | MODIFIER | c.-807G>A| |
S270 |
13 | BAA09g03650 | A09 | 2196229 | C | T | upstream_gene_variant | MODIFIER | c.-2116G>A| |
S203 |
14 | BAA09g03650 | A09 | 2196769 | G | A | upstream_gene_variant | MODIFIER | c.-2656C>T| |
S259 |