Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g26050 | A02 | 14437569 | C | T | synonymous_variant | LOW | c.357G>A|p.Val119Val |
S142 |
2 | BAA02g26050 | A02 | 14438585 | C | T | upstream_gene_variant | MODIFIER | c.-584G>A| |
S308 |
3 | BAA02g26050 | A02 | 14439437 | G | A | upstream_gene_variant | MODIFIER | c.-1436C>T| |
S70 |
4 | BAA02g26050 | A02 | 14439870 | C | T | upstream_gene_variant | MODIFIER | c.-1869G>A| |
S185 |
5 | BAA02g26050 | A02 | 14440136 | C | T | upstream_gene_variant | MODIFIER | c.-2135G>A| |
S282 |
6 | BAA02g26050 | A02 | 14440340 | C | T | upstream_gene_variant | MODIFIER | c.-2339G>A| |
S212 |
7 | BAA02g26050 | A02 | 14440409 | G | A | upstream_gene_variant | MODIFIER | c.-2408C>T| |
S59 |
8 | BAA02g26050 | A02 | 14442192 | C | T | upstream_gene_variant | MODIFIER | c.-4191G>A| |
S40 S49 |
9 | BAA02g26050 | A02 | 14442849 | G | A | upstream_gene_variant | MODIFIER | c.-4848C>T| |
S197 |
10 | BAA02g26050 | A02 | 14442927 | C | T | upstream_gene_variant | MODIFIER | c.-4926G>A| |
S97 |