Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g23060 | A09 | 14536756 | G | A | upstream_gene_variant | MODIFIER | c.-4693G>A| |
S182 |
2 | BAA09g23060 | A09 | 14537328 | G | A | upstream_gene_variant | MODIFIER | c.-4121G>A| |
S288 |
3 | BAA09g23060 | A09 | 14537689 | G | A | upstream_gene_variant | MODIFIER | c.-3760G>A| |
S204 |
4 | BAA09g23060 | A09 | 14537703 | G | A | upstream_gene_variant | MODIFIER | c.-3746G>A| |
S16 |
5 | BAA09g23060 | A09 | 14538060 | C | T | upstream_gene_variant | MODIFIER | c.-3389C>T| |
S235 |
6 | BAA09g23060 | A09 | 14539557 | G | A | upstream_gene_variant | MODIFIER | c.-1892G>A| |
S126 |
7 | BAA09g23060 | A09 | 14540615 | C | T | upstream_gene_variant | MODIFIER | c.-834C>T| |
S283 |
8 | BAA09g23060 | A09 | 14540796 | C | T | upstream_gene_variant | MODIFIER | c.-653C>T| |
S19 |
9 | BAA09g23060 | A09 | 14541868 | G | A | missense_variant | MODERATE | c.336G>A|p.Met112Ile |
S65 |
10 | BAA09g23060 | A09 | 14542324 | G | A | missense_variant | MODERATE | c.409G>A|p.Asp137Asn |
S110 |
11 | BAA09g23060 | A09 | 14544525 | G | A | downstream_gene_variant | MODIFIER | c.*562G>A| |
S16 S233 |