Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04760 | A02 | 2069770 | G | A | downstream_gene_variant | MODIFIER | c.*879C>T| |
S223 |
2 | BAA02g04760 | A02 | 2071217 | G | A | missense_variant | MODERATE | c.107C>T|p.Ser36Leu |
S62 |
3 | BAA02g04760 | A02 | 2071501 | C | T | upstream_gene_variant | MODIFIER | c.-178G>A| |
S199 |
4 | BAA02g04760 | A02 | 2071998 | G | A | upstream_gene_variant | MODIFIER | c.-675C>T| |
S163 |
5 | BAA02g04760 | A02 | 2072350 | G | A | upstream_gene_variant | MODIFIER | c.-1027C>T| |
S45 |
6 | BAA02g04760 | A02 | 2072668 | G | A | upstream_gene_variant | MODIFIER | c.-1345C>T| |
S177 |
7 | BAA02g04760 | A02 | 2072985 | C | T | upstream_gene_variant | MODIFIER | c.-1662G>A| |
S230 |
8 | BAA02g04760 | A02 | 2074157 | G | A | upstream_gene_variant | MODIFIER | c.-2834C>T| |
S269 |
9 | BAA02g04760 | A02 | 2075078 | C | G | upstream_gene_variant | MODIFIER | c.-3755G>C| |
S47 S92 |
10 | BAA02g04760 | A02 | 2075496 | C | T | upstream_gene_variant | MODIFIER | c.-4173G>A| |
S172 S217 |
11 | BAA02g04760 | A02 | 2075788 | C | T | upstream_gene_variant | MODIFIER | c.-4465G>A| |
S287 |