Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08340 | A09 | 4643232 | G | A | missense_variant | MODERATE | c.805C>T|p.Pro269Ser |
S252 |
2 | BAA09g08340 | A09 | 4644302 | G | A | synonymous_variant | LOW | c.258C>T|p.Ala86Ala |
S78 |
3 | BAA09g08340 | A09 | 4646129 | C | T | upstream_gene_variant | MODIFIER | c.-1360G>A| |
S111 |
4 | BAA09g08340 | A09 | 4648386 | C | T | upstream_gene_variant | MODIFIER | c.-3617G>A| |
S171 |
5 | BAA09g08340 | A09 | 4649751 | G | A | upstream_gene_variant | MODIFIER | c.-4982C>T| |
S278 |