Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29460 | A02 | 16867617 | G | A | downstream_gene_variant | MODIFIER | c.*3391C>T| |
S50 |
2 | BAA02g29460 | A02 | 16867994 | G | A | downstream_gene_variant | MODIFIER | c.*3014C>T| |
S68 |
3 | BAA02g29460 | A02 | 16871367 | G | A | missense_variant | MODERATE | c.856C>T|p.Pro286Ser |
S41 |
4 | BAA02g29460 | A02 | 16871475 | G | A | missense_variant | MODERATE | c.748C>T|p.Leu250Phe |
S263 |
5 | BAA02g29460 | A02 | 16873339 | G | A | missense_variant | MODERATE | c.68C>T|p.Ser23Phe |
S298 |
6 | BAA02g29460 | A02 | 16875273 | G | A | upstream_gene_variant | MODIFIER | c.-1867C>T| |
S58 |
7 | BAA02g29460 | A02 | 16875322 | G | A | upstream_gene_variant | MODIFIER | c.-1916C>T| |
S189 |
8 | BAA02g29460 | A02 | 16875653 | G | A | upstream_gene_variant | MODIFIER | c.-2247C>T| |
S110 |
9 | BAA02g29460 | A02 | 16877137 | A | G | upstream_gene_variant | MODIFIER | c.-3731T>C| |
S36 |
10 | BAA02g29460 | A02 | 16877400 | C | T | upstream_gene_variant | MODIFIER | c.-3994G>A| |
S216 |
11 | BAA02g29460 | A02 | 16877625 | C | A | upstream_gene_variant | MODIFIER | c.-4219G>T| |
S62 |
12 | BAA02g29460 | A02 | 16877659 | G | A | upstream_gene_variant | MODIFIER | c.-4253C>T| |
S306 |
13 | BAA02g29460 | A02 | 16877830 | C | T | upstream_gene_variant | MODIFIER | c.-4424G>A| |
S171 |
14 | BAA02g29460 | A02 | 16877930 | C | T | upstream_gene_variant | MODIFIER | c.-4524G>A| |
S162 |