Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16550 | A05 | 9182828 | G | A | downstream_gene_variant | MODIFIER | c.*4732C>T| |
S297 |
2 | BAA05g16550 | A05 | 9183668 | C | T | downstream_gene_variant | MODIFIER | c.*3892G>A| |
S236 |
3 | BAA05g16550 | A05 | 9183676 | G | A | downstream_gene_variant | MODIFIER | c.*3884C>T| |
S115 |
4 | BAA05g16550 | A05 | 9184515 | C | T | downstream_gene_variant | MODIFIER | c.*3045G>A| |
S201 |
5 | BAA05g16550 | A05 | 9186022 | C | T | downstream_gene_variant | MODIFIER | c.*1538G>A| |
S153 S213 |
6 | BAA05g16550 | A05 | 9188597 | G | A | missense_variant | MODERATE | c.1489C>T|p.Leu497Phe |
S238 |
7 | BAA05g16550 | A05 | 9189136 | G | A | missense_variant | MODERATE | c.1025C>T|p.Ser342Phe |
S104 S52 |
8 | BAA05g16550 | A05 | 9189278 | G | A | missense_variant | MODERATE | c.883C>T|p.Pro295Ser |
S23 |
9 | BAA05g16550 | A05 | 9189329 | G | A | missense_variant | MODERATE | c.832C>T|p.Pro278Ser |
S152 |
10 | BAA05g16550 | A05 | 9190866 | G | A | upstream_gene_variant | MODIFIER | c.-456C>T| |
S221 |
11 | BAA05g16550 | A05 | 9191161 | G | A | upstream_gene_variant | MODIFIER | c.-751C>T| |
S274 |
12 | BAA05g16550 | A05 | 9192481 | C | T | upstream_gene_variant | MODIFIER | c.-2071G>A| |
S87 |
13 | BAA05g16550 | A05 | 9192679 | G | A | upstream_gene_variant | MODIFIER | c.-2269C>T| |
S263 |
14 | BAA05g16550 | A05 | 9194184 | C | T | upstream_gene_variant | MODIFIER | c.-3774G>A| |
S8 |
15 | BAA05g16550 | A05 | 9194894 | G | A | upstream_gene_variant | MODIFIER | c.-4484C>T| |
S226 |