Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g47670 | A09 | 51839891 | C | T | upstream_gene_variant | MODIFIER | c.-2858C>T| |
S260 |
2 | BAA09g47670 | A09 | 51840018 | G | A | upstream_gene_variant | MODIFIER | c.-2731G>A| |
S70 |
3 | BAA09g47670 | A09 | 51844555 | G | A | missense_variant | MODERATE | c.937G>A|p.Gly313Ser |
S274 |
4 | BAA09g47670 | A09 | 51844822 | C | T | missense_variant | MODERATE | c.1058C>T|p.Ser353Leu |
S149 |
5 | BAA09g47670 | A09 | 51848460 | C | T | downstream_gene_variant | MODIFIER | c.*3290C>T| |
S232 |
6 | BAA09g47670 | A09 | 51849287 | G | A | downstream_gene_variant | MODIFIER | c.*4117G>A| |
S167 |