Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10020 | A01 | 4523363 | G | A | missense_variant | MODERATE | c.542C>T|p.Ser181Phe |
S28 |
2 | BAA01g10020 | A01 | 4523570 | C | T | missense_variant&splice_region_variant | MODERATE | c.412G>A|p.Ala138Thr |
S264 |
3 | BAA01g10020 | A01 | 4525763 | C | T | upstream_gene_variant | MODIFIER | c.-907G>A| |
S25 |
4 | BAA01g10020 | A01 | 4526025 | C | T | upstream_gene_variant | MODIFIER | c.-1169G>A| |
S99 |
5 | BAA01g10020 | A01 | 4526031 | G | A | upstream_gene_variant | MODIFIER | c.-1175C>T| |
S92 |
6 | BAA01g10020 | A01 | 4526379 | C | T | upstream_gene_variant | MODIFIER | c.-1523G>A| |
S148 S30 S31 |
7 | BAA01g10020 | A01 | 4526477 | C | T | upstream_gene_variant | MODIFIER | c.-1621G>A| |
S210 |
8 | BAA01g10020 | A01 | 4526785 | G | A | upstream_gene_variant | MODIFIER | c.-1929C>T| |
S173 |
9 | BAA01g10020 | A01 | 4527091 | C | T | upstream_gene_variant | MODIFIER | c.-2235G>A| |
S295 |
10 | BAA01g10020 | A01 | 4527738 | C | T | upstream_gene_variant | MODIFIER | c.-2882G>A| |
S39 |
11 | BAA01g10020 | A01 | 4528013 | C | T | upstream_gene_variant | MODIFIER | c.-3157G>A| |
S295 |