Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g08800 | A02 | 3898336 | C | T | downstream_gene_variant | MODIFIER | c.*3005G>A| |
S116 |
2 | BAA02g08800 | A02 | 3901529 | C | T | missense_variant | MODERATE | c.1255G>A|p.Ala419Thr |
S138 |
3 | BAA02g08800 | A02 | 3901569 | T | C | synonymous_variant | LOW | c.1215A>G|p.Gly405Gly |
S144 |
4 | BAA02g08800 | A02 | 3901941 | C | T | missense_variant | MODERATE | c.1006G>A|p.Gly336Arg |
S167 |
5 | BAA02g08800 | A02 | 3902151 | C | T | missense_variant | MODERATE | c.881G>A|p.Ser294Asn |
S274 |
6 | BAA02g08800 | A02 | 3902405 | G | A | missense_variant | MODERATE | c.716C>T|p.Pro239Leu |
S295 |
7 | BAA02g08800 | A02 | 3902917 | G | A | synonymous_variant | LOW | c.486C>T|p.Cys162Cys |
S105 S106 |
8 | BAA02g08800 | A02 | 3903826 | G | A | splice_region_variant&intron_variant | LOW | c.162+7C>T| |
S293 |
9 | BAA02g08800 | A02 | 3904074 | C | T | missense_variant | MODERATE | c.4G>A|p.Asp2Asn |
S25 |
10 | BAA02g08800 | A02 | 3905297 | G | A | upstream_gene_variant | MODIFIER | c.-1220C>T| |
S187 |
11 | BAA02g08800 | A02 | 3905326 | G | A | upstream_gene_variant | MODIFIER | c.-1249C>T| |
S119 |
12 | BAA02g08800 | A02 | 3905632 | G | A | upstream_gene_variant | MODIFIER | c.-1555C>T| |
S237 |
13 | BAA02g08800 | A02 | 3906672 | G | A | upstream_gene_variant | MODIFIER | c.-2595C>T| |
S156 |
14 | BAA02g08800 | A02 | 3907380 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S295 |