Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18330 | A02 | 9284052 | T | A | upstream_gene_variant | MODIFIER | c.-4907T>A| |
S140 |
2 | BAA02g18330 | A02 | 9285254 | C | T | upstream_gene_variant | MODIFIER | c.-3705C>T| |
S178 |
3 | BAA02g18330 | A02 | 9286071 | G | A | upstream_gene_variant | MODIFIER | c.-2888G>A| |
S45 |
4 | BAA02g18330 | A02 | 9286103 | C | T | upstream_gene_variant | MODIFIER | c.-2856C>T| |
S284 |
5 | BAA02g18330 | A02 | 9286883 | C | T | upstream_gene_variant | MODIFIER | c.-2076C>T| |
S71 |
6 | BAA02g18330 | A02 | 9287240 | C | T | upstream_gene_variant | MODIFIER | c.-1719C>T| |
S8 |
7 | BAA02g18330 | A02 | 9287258 | C | T | upstream_gene_variant | MODIFIER | c.-1701C>T| |
S165 |
8 | BAA02g18330 | A02 | 9287466 | G | A | upstream_gene_variant | MODIFIER | c.-1493G>A| |
S291 |
9 | BAA02g18330 | A02 | 9287910 | C | T | upstream_gene_variant | MODIFIER | c.-1049C>T| |
S152 |
10 | BAA02g18330 | A02 | 9288761 | C | T | upstream_gene_variant | MODIFIER | c.-198C>T| |
S144 |
11 | BAA02g18330 | A02 | 9289028 | C | T | missense_variant | MODERATE | c.70C>T|p.Pro24Ser |
S46 |