Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25580 | A05 | 30383438 | C | T | upstream_gene_variant | MODIFIER | c.-3875C>T| |
S56 |
2 | BAA05g25580 | A05 | 30384740 | G | A | upstream_gene_variant | MODIFIER | c.-2573G>A| |
S16 |
3 | BAA05g25580 | A05 | 30385570 | C | T | upstream_gene_variant | MODIFIER | c.-1743C>T| |
S84 S93 |
4 | BAA05g25580 | A05 | 30385973 | C | T | upstream_gene_variant | MODIFIER | c.-1340C>T| |
S206 S26 |
5 | BAA05g25580 | A05 | 30386181 | G | A | upstream_gene_variant | MODIFIER | c.-1132G>A| |
S136 |
6 | BAA05g25580 | A05 | 30386817 | G | A | upstream_gene_variant | MODIFIER | c.-496G>A| |
S262 |
7 | BAA05g25580 | A05 | 30386819 | G | A | upstream_gene_variant | MODIFIER | c.-494G>A| |
S180 |
8 | BAA05g25580 | A05 | 30387235 | G | A | upstream_gene_variant | MODIFIER | c.-78G>A| |
S249 |
9 | BAA05g25580 | A05 | 30388142 | C | T | missense_variant | MODERATE | c.649C>T|p.Pro217Ser |
S198 |
10 | BAA05g25580 | A05 | 30388651 | C | T | downstream_gene_variant | MODIFIER | c.*317C>T| |
S181 |
11 | BAA05g25580 | A05 | 30388837 | G | A | downstream_gene_variant | MODIFIER | c.*503G>A| |
S5 |