Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g07770 | A09 | 4288627 | C | T | downstream_gene_variant | MODIFIER | c.*1024G>A| |
S188 S276 |
2 | BAA09g07770 | A09 | 4290303 | G | A | missense_variant | MODERATE | c.803C>T|p.Ser268Leu |
S270 |
3 | BAA09g07770 | A09 | 4291019 | G | A | synonymous_variant | LOW | c.408C>T|p.Ser136Ser |
S228 |
4 | BAA09g07770 | A09 | 4291162 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.266-1G>A| |
S208 S219 |
5 | BAA09g07770 | A09 | 4295375 | G | A | upstream_gene_variant | MODIFIER | c.-3764C>T| |
S159 S299 |
6 | BAA09g07770 | A09 | 4295787 | G | A | upstream_gene_variant | MODIFIER | c.-4176C>T| |
S151 |
7 | BAA09g07770 | A09 | 4295862 | C | T | upstream_gene_variant | MODIFIER | c.-4251G>A| |
S148 |
8 | BAA09g07770 | A09 | 4296231 | C | T | upstream_gene_variant | MODIFIER | c.-4620G>A| |
S183 S198 |
9 | BAA09g07770 | A09 | 4296456 | C | T | upstream_gene_variant | MODIFIER | c.-4845G>A| |
S134 |