Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g01200 | A02 | 555207 | C | T | upstream_gene_variant | MODIFIER | c.-3592C>T| |
S278 |
2 | BAA02g01200 | A02 | 557626 | G | A | upstream_gene_variant | MODIFIER | c.-1173G>A| |
S134 |
3 | BAA02g01200 | A02 | 559942 | G | A | missense_variant&splice_region_variant | MODERATE | c.839G>A|p.Gly280Glu |
S33 |
4 | BAA02g01200 | A02 | 560105 | G | A | synonymous_variant | LOW | c.912G>A|p.Arg304Arg |
S87 |
5 | BAA02g01200 | A02 | 560233 | C | T | missense_variant | MODERATE | c.1040C>T|p.Thr347Ile |
S277 |
6 | BAA02g01200 | A02 | 564455 | C | T | synonymous_variant | LOW | c.1692C>T|p.Leu564Leu |
S292 |
7 | BAA02g01200 | A02 | 564461 | C | T | synonymous_variant | LOW | c.1698C>T|p.Ile566Ile |
S250 |
8 | BAA02g01200 | A02 | 565015 | G | A | synonymous_variant | LOW | c.2091G>A|p.Glu697Glu |
S98 |
9 | BAA02g01200 | A02 | 565517 | G | A | missense_variant | MODERATE | c.2501G>A|p.Gly834Asp |
S149 |