Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g00140 | A02 | 102582 | G | A | downstream_gene_variant | MODIFIER | c.*4576C>T| |
S232 |
2 | BAA02g00140 | A02 | 102803 | G | A | downstream_gene_variant | MODIFIER | c.*4355C>T| |
S53 |
3 | BAA02g00140 | A02 | 107045 | C | T | downstream_gene_variant | MODIFIER | c.*113G>A| |
S65 |
4 | BAA02g00140 | A02 | 107676 | G | A | upstream_gene_variant | MODIFIER | c.-36C>T| |
S47 |
5 | BAA02g00140 | A02 | 108892 | C | T | upstream_gene_variant | MODIFIER | c.-1252G>A| |
S69 |
6 | BAA02g00140 | A02 | 108927 | G | A | upstream_gene_variant | MODIFIER | c.-1287C>T| |
S282 |
7 | BAA02g00140 | A02 | 110093 | G | A | upstream_gene_variant | MODIFIER | c.-2453C>T| |
S266 |
8 | BAA02g00140 | A02 | 110820 | G | A | upstream_gene_variant | MODIFIER | c.-3180C>T| |
S11 |
9 | BAA02g00140 | A02 | 111036 | C | T | upstream_gene_variant | MODIFIER | c.-3396G>A| |
S71 |