Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g13220 | A02 | 5996548 | G | A | downstream_gene_variant | MODIFIER | c.*3038C>T| |
S7 |
2 | BAA02g13220 | A02 | 5997569 | G | A | downstream_gene_variant | MODIFIER | c.*2017C>T| |
S263 |
3 | BAA02g13220 | A02 | 5997796 | G | A | downstream_gene_variant | MODIFIER | c.*1790C>T| |
S146 |
4 | BAA02g13220 | A02 | 5999612 | G | A | missense_variant | MODERATE | c.166C>T|p.Pro56Ser |
S125 |
5 | BAA02g13220 | A02 | 6000205 | C | T | upstream_gene_variant | MODIFIER | c.-428G>A| |
S55 |
6 | BAA02g13220 | A02 | 6001029 | C | T | upstream_gene_variant | MODIFIER | c.-1252G>A| |
S299 |
7 | BAA02g13220 | A02 | 6003480 | G | A | upstream_gene_variant | MODIFIER | c.-3703C>T| |
S148 S30 S31 |
8 | BAA02g13220 | A02 | 6003511 | G | A | upstream_gene_variant | MODIFIER | c.-3734C>T| |
S295 |
9 | BAA02g13220 | A02 | 6004420 | C | T | upstream_gene_variant | MODIFIER | c.-4643G>A| |
S139 |