Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g39760 | A01 | 26411695 | C | T | downstream_gene_variant | MODIFIER | c.*4952G>A| |
S275 |
2 | BAA01g39760 | A01 | 26412000 | G | A | downstream_gene_variant | MODIFIER | c.*4647C>T| |
S60 |
3 | BAA01g39760 | A01 | 26412294 | C | T | downstream_gene_variant | MODIFIER | c.*4353G>A| |
S260 |
4 | BAA01g39760 | A01 | 26412458 | G | A | downstream_gene_variant | MODIFIER | c.*4189C>T| |
S212 |
5 | BAA01g39760 | A01 | 26412703 | C | T | downstream_gene_variant | MODIFIER | c.*3944G>A| |
S92 |
6 | BAA01g39760 | A01 | 26413347 | C | T | downstream_gene_variant | MODIFIER | c.*3300G>A| |
S183 S198 |
7 | BAA01g39760 | A01 | 26413620 | C | T | downstream_gene_variant | MODIFIER | c.*3027G>A| |
S56 |
8 | BAA01g39760 | A01 | 26413705 | G | A | downstream_gene_variant | MODIFIER | c.*2942C>T| |
S117 |
9 | BAA01g39760 | A01 | 26415183 | C | T | downstream_gene_variant | MODIFIER | c.*1464G>A| |
S210 S225 |
10 | BAA01g39760 | A01 | 26416007 | C | T | downstream_gene_variant | MODIFIER | c.*640G>A| |
S72 S78 |
11 | BAA01g39760 | A01 | 26416221 | C | T | downstream_gene_variant | MODIFIER | c.*426G>A| |
S183 S198 |
12 | BAA01g39760 | A01 | 26416791 | C | T | stop_gained | HIGH | c.1092G>A|p.Trp364* |
S162 |
13 | BAA01g39760 | A01 | 26417123 | C | G | intron_variant | MODIFIER | c.1073-313G>C| |
S54 |
14 | BAA01g39760 | A01 | 26417164 | G | A | intron_variant | MODIFIER | c.1073-354C>T| |
S116 |
15 | BAA01g39760 | A01 | 26418705 | C | T | missense_variant | MODERATE | c.943G>A|p.Glu315Lys |
S174 S27 |
16 | BAA01g39760 | A01 | 26419173 | G | A | synonymous_variant | LOW | c.600C>T|p.Val200Val |
S176 |
17 | BAA01g39760 | A01 | 26419565 | C | T | missense_variant | MODERATE | c.208G>A|p.Asp70Asn |
S161 |
18 | BAA01g39760 | A01 | 26419985 | G | A | missense_variant | MODERATE | c.79C>T|p.Leu27Phe |
S271 |
19 | BAA01g39760 | A01 | 26420838 | G | A | upstream_gene_variant | MODIFIER | c.-775C>T| |
S116 |
20 | BAA01g39760 | A01 | 26421747 | C | T | upstream_gene_variant | MODIFIER | c.-1684G>A| |
S233 |