Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10770 | A02 | 4817496 | C | T | missense_variant | MODERATE | c.571G>A|p.Asp191Asn |
S33 |
2 | BAA02g10770 | A02 | 4817846 | G | A | missense_variant | MODERATE | c.221C>T|p.Ser74Leu |
S244 |
3 | BAA02g10770 | A02 | 4820066 | G | A | upstream_gene_variant | MODIFIER | c.-2000C>T| |
S37 |
4 | BAA02g10770 | A02 | 4820284 | C | T | upstream_gene_variant | MODIFIER | c.-2218G>A| |
S129 |
5 | BAA02g10770 | A02 | 4820303 | G | A | upstream_gene_variant | MODIFIER | c.-2237C>T| |
S236 |
6 | BAA02g10770 | A02 | 4822708 | C | T | upstream_gene_variant | MODIFIER | c.-4642G>A| |
S278 |