Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29130 | A02 | 16630457 | C | T | downstream_gene_variant | MODIFIER | c.*4713G>A| |
S54 |
2 | BAA02g29130 | A02 | 16630950 | C | T | downstream_gene_variant | MODIFIER | c.*4220G>A| |
S171 |
3 | BAA02g29130 | A02 | 16631144 | G | A | downstream_gene_variant | MODIFIER | c.*4026C>T| |
S187 |
4 | BAA02g29130 | A02 | 16632557 | G | A | downstream_gene_variant | MODIFIER | c.*2613C>T| |
S10 |
5 | BAA02g29130 | A02 | 16633371 | C | T | downstream_gene_variant | MODIFIER | c.*1799G>A| |
S161 |
6 | BAA02g29130 | A02 | 16634038 | C | T | downstream_gene_variant | MODIFIER | c.*1132G>A| |
S32 |
7 | BAA02g29130 | A02 | 16635731 | G | A | synonymous_variant | LOW | c.1108C>T|p.Leu370Leu |
S153 S213 |
8 | BAA02g29130 | A02 | 16636749 | G | A | missense_variant | MODERATE | c.653C>T|p.Ser218Phe |
S272 |
9 | BAA02g29130 | A02 | 16637482 | G | A | synonymous_variant | LOW | c.243C>T|p.Asp81Asp |
S153 S213 |
10 | BAA02g29130 | A02 | 16637552 | G | A | missense_variant | MODERATE | c.173C>T|p.Ser58Phe |
S17 |
11 | BAA02g29130 | A02 | 16637652 | G | A | missense_variant | MODERATE | c.73C>T|p.Leu25Phe |
S209 |
12 | BAA02g29130 | A02 | 16638349 | G | A | upstream_gene_variant | MODIFIER | c.-625C>T| |
S148 S210 S30 S31 |