Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42150 | A02 | 35136151 | A | T | upstream_gene_variant | MODIFIER | c.-202A>T| |
S292 |
2 | BAA02g42150 | A02 | 35136307 | C | T | upstream_gene_variant | MODIFIER | c.-46C>T| |
S159 S187 S188 S243 S276 S299 |
3 | BAA02g42150 | A02 | 35136913 | C | T | missense_variant | MODERATE | c.169C>T|p.His57Tyr |
S283 |
4 | BAA02g42150 | A02 | 35137169 | A | C | intron_variant | MODIFIER | c.312-34A>C| |
S155 S165 S211 |
5 | BAA02g42150 | A02 | 35137950 | C | T | intron_variant | MODIFIER | c.424-11C>T| |
S270 |
6 | BAA02g42150 | A02 | 35138878 | G | A | downstream_gene_variant | MODIFIER | c.*666G>A| |
S199 |
7 | BAA02g42150 | A02 | 35141255 | C | T | downstream_gene_variant | MODIFIER | c.*3043C>T| |
S139 |
8 | BAA02g42150 | A02 | 35141667 | C | T | downstream_gene_variant | MODIFIER | c.*3455C>T| |
S17 |
9 | BAA02g42150 | A02 | 35141991 | C | T | downstream_gene_variant | MODIFIER | c.*3779C>T| |
S158 |