Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g10490 | A09 | 5731620 | C | T | missense_variant | MODERATE | c.769G>A|p.Asp257Asn |
S36 |
2 | BAA09g10490 | A09 | 5732328 | C | T | synonymous_variant | LOW | c.345G>A|p.Gln115Gln |
S17 |
3 | BAA09g10490 | A09 | 5736371 | C | T | upstream_gene_variant | MODIFIER | c.-3431G>A| |
S87 |
4 | BAA09g10490 | A09 | 5736588 | G | A | upstream_gene_variant | MODIFIER | c.-3648C>T| |
S296 |
5 | BAA09g10490 | A09 | 5737233 | G | A | upstream_gene_variant | MODIFIER | c.-4293C>T| |
S301 S304 |