Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g41860 | A02 | 34980034 | C | T | upstream_gene_variant | MODIFIER | c.-4363C>T| |
S180 |
2 | BAA02g41860 | A02 | 34980109 | C | T | upstream_gene_variant | MODIFIER | c.-4288C>T| |
S77 S82 |
3 | BAA02g41860 | A02 | 34980612 | C | T | upstream_gene_variant | MODIFIER | c.-3785C>T| |
S61 |
4 | BAA02g41860 | A02 | 34981339 | C | T | upstream_gene_variant | MODIFIER | c.-3058C>T| |
S241 |
5 | BAA02g41860 | A02 | 34981518 | G | A | upstream_gene_variant | MODIFIER | c.-2879G>A| |
S176 |
6 | BAA02g41860 | A02 | 34981800 | C | T | upstream_gene_variant | MODIFIER | c.-2597C>T| |
S18 |
7 | BAA02g41860 | A02 | 34982995 | C | T | upstream_gene_variant | MODIFIER | c.-1402C>T| |
S275 |
8 | BAA02g41860 | A02 | 34983149 | G | A | upstream_gene_variant | MODIFIER | c.-1248G>A| |
S34 |
9 | BAA02g41860 | A02 | 34984249 | G | A | upstream_gene_variant | MODIFIER | c.-148G>A| |
S288 |
10 | BAA02g41860 | A02 | 34984449 | G | A | missense_variant | MODERATE | c.53G>A|p.Gly18Asp |
S52 |
11 | BAA02g41860 | A02 | 34986238 | C | T | downstream_gene_variant | MODIFIER | c.*1512C>T| |
S124 |