Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g15460 | A01 | 7465358 | C | T | upstream_gene_variant | MODIFIER | c.-3718C>T| |
S289 S290 |
2 | BAA01g15460 | A01 | 7465415 | C | T | upstream_gene_variant | MODIFIER | c.-3661C>T| |
S296 |
3 | BAA01g15460 | A01 | 7465464 | C | T | upstream_gene_variant | MODIFIER | c.-3612C>T| |
S82 S92 |
4 | BAA01g15460 | A01 | 7465937 | C | T | upstream_gene_variant | MODIFIER | c.-3139C>T| |
S44 |
5 | BAA01g15460 | A01 | 7466375 | C | T | upstream_gene_variant | MODIFIER | c.-2701C>T| |
S231 |
6 | BAA01g15460 | A01 | 7467047 | G | T | upstream_gene_variant | MODIFIER | c.-2029G>T| |
S274 |
7 | BAA01g15460 | A01 | 7467128 | C | T | upstream_gene_variant | MODIFIER | c.-1948C>T| |
S291 |
8 | BAA01g15460 | A01 | 7468712 | C | T | upstream_gene_variant | MODIFIER | c.-364C>T| |
S65 |
9 | BAA01g15460 | A01 | 7469060 | G | A | upstream_gene_variant | MODIFIER | c.-16G>A| |
S23 |
10 | BAA01g15460 | A01 | 7470262 | G | A | synonymous_variant | LOW | c.777G>A|p.Ala259Ala |
S163 |
11 | BAA01g15460 | A01 | 7470481 | C | T | missense_variant | MODERATE | c.859C>T|p.Pro287Ser |
S305 |
12 | BAA01g15460 | A01 | 7470704 | C | T | synonymous_variant | LOW | c.972C>T|p.Val324Val |
S289 S290 |