Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g44260 | A02 | 36521027 | C | T | upstream_gene_variant | MODIFIER | c.-4184C>T| |
S228 |
2 | BAA02g44260 | A02 | 36521109 | G | A | upstream_gene_variant | MODIFIER | c.-4102G>A| |
S225 |
3 | BAA02g44260 | A02 | 36522907 | C | T | upstream_gene_variant | MODIFIER | c.-2304C>T| |
S242 |
4 | BAA02g44260 | A02 | 36523567 | G | A | upstream_gene_variant | MODIFIER | c.-1644G>A| |
S37 |
5 | BAA02g44260 | A02 | 36523633 | G | A | upstream_gene_variant | MODIFIER | c.-1578G>A| |
S54 |
6 | BAA02g44260 | A02 | 36523713 | G | A | upstream_gene_variant | MODIFIER | c.-1498G>A| |
S225 |
7 | BAA02g44260 | A02 | 36523730 | C | T | upstream_gene_variant | MODIFIER | c.-1481C>T| |
S270 |
8 | BAA02g44260 | A02 | 36523994 | G | A | upstream_gene_variant | MODIFIER | c.-1217G>A| |
S288 |
9 | BAA02g44260 | A02 | 36524024 | G | A | upstream_gene_variant | MODIFIER | c.-1187G>A| |
S7 |
10 | BAA02g44260 | A02 | 36524957 | G | A | upstream_gene_variant | MODIFIER | c.-254G>A| |
S157 S163 |
11 | BAA02g44260 | A02 | 36525086 | G | A | upstream_gene_variant | MODIFIER | c.-125G>A| |
S45 |
12 | BAA02g44260 | A02 | 36525357 | G | A | stop_gained | HIGH | c.147G>A|p.Trp49* |
S209 |
13 | BAA02g44260 | A02 | 36525405 | C | T | synonymous_variant | LOW | c.195C>T|p.Tyr65Tyr |
S123 |
14 | BAA02g44260 | A02 | 36525859 | G | A | missense_variant | MODERATE | c.649G>A|p.Glu217Lys |
S279 |
15 | BAA02g44260 | A02 | 36526083 | C | T | synonymous_variant | LOW | c.873C>T|p.Gly291Gly |
S218 |