Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g39000 | A02 | 33211434 | G | A | missense_variant | MODERATE | c.1103C>T|p.Pro368Leu |
S215 |
2 | BAA02g39000 | A02 | 33212122 | G | A | missense_variant | MODERATE | c.572C>T|p.Thr191Ile |
S223 |
3 | BAA02g39000 | A02 | 33212218 | C | T | missense_variant | MODERATE | c.476G>A|p.Gly159Glu |
S82 S92 |
4 | BAA02g39000 | A02 | 33212280 | G | A | synonymous_variant | LOW | c.414C>T|p.Asn138Asn |
S256 |
5 | BAA02g39000 | A02 | 33213100 | C | T | upstream_gene_variant | MODIFIER | c.-266G>A| |
S172 S217 |
6 | BAA02g39000 | A02 | 33214073 | C | T | upstream_gene_variant | MODIFIER | c.-1239G>A| |
S124 |
7 | BAA02g39000 | A02 | 33215857 | C | T | upstream_gene_variant | MODIFIER | c.-3023G>A| |
S68 |
8 | BAA02g39000 | A02 | 33216522 | G | A | upstream_gene_variant | MODIFIER | c.-3688C>T| |
S177 |
9 | BAA02g39000 | A02 | 33217499 | C | T | upstream_gene_variant | MODIFIER | c.-4665G>A| |
S303 |
10 | BAA02g39000 | A02 | 33217568 | C | T | upstream_gene_variant | MODIFIER | c.-4734G>A| |
S181 |
11 | BAA02g39000 | A02 | 33217628 | G | A | upstream_gene_variant | MODIFIER | c.-4794C>T| |
S264 |