Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09930 | A02 | 4377055 | G | A | missense_variant | MODERATE | c.2528C>T|p.Ser843Phe |
S148 S30 S31 |
2 | BAA02g09930 | A02 | 4377137 | C | T | missense_variant | MODERATE | c.2446G>A|p.Asp816Asn |
S292 |
3 | BAA02g09930 | A02 | 4378541 | G | A | missense_variant | MODERATE | c.1490C>T|p.Ser497Phe |
S23 |
4 | BAA02g09930 | A02 | 4379542 | C | T | synonymous_variant | LOW | c.957G>A|p.Gln319Gln |
S65 |
5 | BAA02g09930 | A02 | 4381441 | C | T | splice_donor_variant&intron_variant | HIGH | c.135+1G>A| |
S87 |
6 | BAA02g09930 | A02 | 4381547 | G | A | synonymous_variant | LOW | c.30C>T|p.Pro10Pro |
S4 |
7 | BAA02g09930 | A02 | 4383629 | C | T | upstream_gene_variant | MODIFIER | c.-2053G>A| |
S139 |
8 | BAA02g09930 | A02 | 4384545 | G | A | upstream_gene_variant | MODIFIER | c.-2969C>T| |
S291 |
9 | BAA02g09930 | A02 | 4386126 | G | T | upstream_gene_variant | MODIFIER | c.-4550C>A| |
S1 S90 |