Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42100 | A02 | 35108711 | G | A | downstream_gene_variant | MODIFIER | c.*1826C>T| |
S4 |
2 | BAA02g42100 | A02 | 35108921 | C | T | downstream_gene_variant | MODIFIER | c.*1616G>A| |
S264 |
3 | BAA02g42100 | A02 | 35109160 | A | C | downstream_gene_variant | MODIFIER | c.*1377T>G| |
S172 S217 |
4 | BAA02g42100 | A02 | 35109687 | G | A | downstream_gene_variant | MODIFIER | c.*850C>T| |
S50 |
5 | BAA02g42100 | A02 | 35109734 | G | A | downstream_gene_variant | MODIFIER | c.*803C>T| |
S176 |
6 | BAA02g42100 | A02 | 35110805 | C | T | missense_variant | MODERATE | c.1331G>A|p.Gly444Glu |
S46 |
7 | BAA02g42100 | A02 | 35112744 | G | A | upstream_gene_variant | MODIFIER | c.-76C>T| |
S148 S30 S31 |
8 | BAA02g42100 | A02 | 35112991 | C | T | upstream_gene_variant | MODIFIER | c.-323G>A| |
S299 |
9 | BAA02g42100 | A02 | 35113345 | C | T | upstream_gene_variant | MODIFIER | c.-677G>A| |
S266 |
10 | BAA02g42100 | A02 | 35116973 | C | T | upstream_gene_variant | MODIFIER | c.-4305G>A| |
S249 |