Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19030 | A02 | 9840061 | C | T | downstream_gene_variant | MODIFIER | c.*4093G>A| |
S16 |
2 | BAA02g19030 | A02 | 9840812 | C | T | downstream_gene_variant | MODIFIER | c.*3342G>A| |
S158 |
3 | BAA02g19030 | A02 | 9844318 | G | A | missense_variant | MODERATE | c.2240C>T|p.Ala747Val |
S205 |
4 | BAA02g19030 | A02 | 9845790 | C | T | missense_variant | MODERATE | c.1010G>A|p.Cys337Tyr |
S18 |
5 | BAA02g19030 | A02 | 9846109 | C | T | missense_variant | MODERATE | c.691G>A|p.Asp231Asn |
S130 |
6 | BAA02g19030 | A02 | 9846173 | G | A | synonymous_variant | LOW | c.627C>T|p.Leu209Leu |
S247 |
7 | BAA02g19030 | A02 | 9846688 | C | T | missense_variant | MODERATE | c.112G>A|p.Asp38Asn |
S71 |
8 | BAA02g19030 | A02 | 9848199 | C | T | upstream_gene_variant | MODIFIER | c.-1400G>A| |
S87 |
9 | BAA02g19030 | A02 | 9851010 | C | T | upstream_gene_variant | MODIFIER | c.-4211G>A| |
S277 |
10 | BAA02g19030 | A02 | 9851343 | C | T | upstream_gene_variant | MODIFIER | c.-4544G>A| |
S175 |