Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g29770 | A02 | 17102304 | C | T | upstream_gene_variant | MODIFIER | c.-4861C>T| |
S277 |
2 | BAA02g29770 | A02 | 17102704 | G | A | upstream_gene_variant | MODIFIER | c.-4461G>A| |
S204 S210 S225 |
3 | BAA02g29770 | A02 | 17107262 | C | T | intron_variant | MODIFIER | c.43-35C>T| |
S208 S93 |
4 | BAA02g29770 | A02 | 17110022 | G | A | intron_variant | MODIFIER | c.148-2307G>A| |
S298 |
5 | BAA02g29770 | A02 | 17113056 | T | G | missense_variant | MODERATE | c.592T>G|p.Cys198Gly |
S287 |
6 | BAA02g29770 | A02 | 17113072 | C | T | missense_variant | MODERATE | c.608C>T|p.Ala203Val |
S152 |
7 | BAA02g29770 | A02 | 17113685 | G | A | missense_variant | MODERATE | c.1055G>A|p.Gly352Glu |
S159 S243 |
8 | BAA02g29770 | A02 | 17115818 | G | A | downstream_gene_variant | MODIFIER | c.*1775G>A| |
S235 |
9 | BAA02g29770 | A02 | 17116037 | G | A | downstream_gene_variant | MODIFIER | c.*1994G>A| |
S95 |
10 | BAA02g29770 | A02 | 17119012 | G | A | downstream_gene_variant | MODIFIER | c.*4969G>A| |
S61 |