Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46610 | A09 | 51286916 | C | T | upstream_gene_variant | MODIFIER | c.-1012C>T| |
S195 |
2 | BAA09g46610 | A09 | 51288961 | A | C | intron_variant | MODIFIER | c.405-159A>C| |
S76 |
3 | BAA09g46610 | A09 | 51289370 | C | T | downstream_gene_variant | MODIFIER | c.*178C>T| |
S289 |
4 | BAA09g46610 | A09 | 51290583 | G | A | downstream_gene_variant | MODIFIER | c.*1391G>A| |
S163 |
5 | BAA09g46610 | A09 | 51291507 | G | A | downstream_gene_variant | MODIFIER | c.*2315G>A| |
S62 |
6 | BAA09g46610 | A09 | 51291707 | C | T | downstream_gene_variant | MODIFIER | c.*2515C>T| |
S30 S31 |
7 | BAA09g46610 | A09 | 51292560 | G | A | downstream_gene_variant | MODIFIER | c.*3368G>A| |
S270 |
8 | BAA09g46610 | A09 | 51292919 | G | A | downstream_gene_variant | MODIFIER | c.*3727G>A| |
S171 |
9 | BAA09g46610 | A09 | 51292979 | C | T | downstream_gene_variant | MODIFIER | c.*3787C>T| |
S153 |