Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g08220 | A09 | 4590745 | C | T | missense_variant | MODERATE | c.28G>A|p.Ala10Thr |
S270 |
2 | BAA09g08220 | A09 | 4592090 | G | A | upstream_gene_variant | MODIFIER | c.-1318C>T| |
S202 |
3 | BAA09g08220 | A09 | 4592492 | G | A | upstream_gene_variant | MODIFIER | c.-1720C>T| |
S225 S73 |
4 | BAA09g08220 | A09 | 4592629 | G | A | upstream_gene_variant | MODIFIER | c.-1857C>T| |
S28 |
5 | BAA09g08220 | A09 | 4592639 | C | T | upstream_gene_variant | MODIFIER | c.-1867G>A| |
S168 |
6 | BAA09g08220 | A09 | 4592861 | G | A | upstream_gene_variant | MODIFIER | c.-2089C>T| |
S66 |
7 | BAA09g08220 | A09 | 4593277 | C | T | upstream_gene_variant | MODIFIER | c.-2505G>A| |
S48 |
8 | BAA09g08220 | A09 | 4595456 | G | A | upstream_gene_variant | MODIFIER | c.-4684C>T| |
S165 |
9 | BAA09g08220 | A09 | 4595572 | G | A | upstream_gene_variant | MODIFIER | c.-4800C>T| |
S238 |