Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g56990 | A09 | 56400285 | C | T | upstream_gene_variant | MODIFIER | c.-4517C>T| |
S192 |
2 | BAA09g56990 | A09 | 56400346 | C | T | upstream_gene_variant | MODIFIER | c.-4456C>T| |
S275 |
3 | BAA09g56990 | A09 | 56400472 | G | A | upstream_gene_variant | MODIFIER | c.-4330G>A| |
S25 |
4 | BAA09g56990 | A09 | 56400701 | G | A | upstream_gene_variant | MODIFIER | c.-4101G>A| |
S88 |
5 | BAA09g56990 | A09 | 56400781 | G | A | upstream_gene_variant | MODIFIER | c.-4021G>A| |
S235 |
6 | BAA09g56990 | A09 | 56401897 | C | T | upstream_gene_variant | MODIFIER | c.-2905C>T| |
S114 |
7 | BAA09g56990 | A09 | 56402015 | G | A | upstream_gene_variant | MODIFIER | c.-2787G>A| |
S88 |
8 | BAA09g56990 | A09 | 56404221 | G | A | upstream_gene_variant | MODIFIER | c.-581G>A| |
S165 |
9 | BAA09g56990 | A09 | 56404349 | T | G | upstream_gene_variant | MODIFIER | c.-453T>G| |
S118 S137 S175 S196 S199 S204 S215 S25 S274 S41 S56 S64 |
10 | BAA09g56990 | A09 | 56405010 | C | T | missense_variant | MODERATE | c.209C>T|p.Pro70Leu |
S296 |
11 | BAA09g56990 | A09 | 56405901 | C | T | missense_variant | MODERATE | c.1100C>T|p.Pro367Leu |
S183 S198 |