Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06300 | A02 | 2664893 | C | T | upstream_gene_variant | MODIFIER | c.-4970C>T| |
S289 S290 |
2 | BAA02g06300 | A02 | 2665271 | C | T | upstream_gene_variant | MODIFIER | c.-4592C>T| |
S243 |
3 | BAA02g06300 | A02 | 2665459 | G | A | upstream_gene_variant | MODIFIER | c.-4404G>A| |
S125 |
4 | BAA02g06300 | A02 | 2665531 | G | A | upstream_gene_variant | MODIFIER | c.-4332G>A| |
S282 |
5 | BAA02g06300 | A02 | 2666113 | G | A | upstream_gene_variant | MODIFIER | c.-3750G>A| |
S206 S26 |
6 | BAA02g06300 | A02 | 2667152 | C | T | upstream_gene_variant | MODIFIER | c.-2711C>T| |
S65 |
7 | BAA02g06300 | A02 | 2667708 | C | T | upstream_gene_variant | MODIFIER | c.-2155C>T| |
S1 S90 |
8 | BAA02g06300 | A02 | 2667927 | G | A | upstream_gene_variant | MODIFIER | c.-1936G>A| |
S207 |
9 | BAA02g06300 | A02 | 2671949 | C | T | missense_variant | MODERATE | c.1459C>T|p.Pro487Ser |
S13 |
10 | BAA02g06300 | A02 | 2673700 | C | T | downstream_gene_variant | MODIFIER | c.*1659C>T| |
S33 |
11 | BAA02g06300 | A02 | 2674286 | C | T | downstream_gene_variant | MODIFIER | c.*2245C>T| |
S284 |