Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g30350 | A02 | 17655538 | G | A | upstream_gene_variant | MODIFIER | c.-4513G>A| |
S217 |
2 | BAA02g30350 | A02 | 17656884 | G | A | upstream_gene_variant | MODIFIER | c.-3167G>A| |
S37 |
3 | BAA02g30350 | A02 | 17656949 | C | T | upstream_gene_variant | MODIFIER | c.-3102C>T| |
S266 |
4 | BAA02g30350 | A02 | 17657444 | G | A | upstream_gene_variant | MODIFIER | c.-2607G>A| |
S79 S84 |
5 | BAA02g30350 | A02 | 17658036 | G | A | upstream_gene_variant | MODIFIER | c.-2015G>A| |
S169 |
6 | BAA02g30350 | A02 | 17658354 | G | A | upstream_gene_variant | MODIFIER | c.-1697G>A| |
S125 |
7 | BAA02g30350 | A02 | 17659831 | G | A | upstream_gene_variant | MODIFIER | c.-220G>A| |
S256 |
8 | BAA02g30350 | A02 | 17659838 | G | A | upstream_gene_variant | MODIFIER | c.-213G>A| |
S293 |
9 | BAA02g30350 | A02 | 17660111 | G | A | missense_variant | MODERATE | c.61G>A|p.Val21Ile |
S159 S243 |
10 | BAA02g30350 | A02 | 17660357 | C | T | missense_variant | MODERATE | c.307C>T|p.His103Tyr |
S175 |
11 | BAA02g30350 | A02 | 17660444 | G | A | missense_variant | MODERATE | c.394G>A|p.Ala132Thr |
S70 |
12 | BAA02g30350 | A02 | 17660480 | G | A | missense_variant | MODERATE | c.430G>A|p.Val144Ile |
S48 |
13 | BAA02g30350 | A02 | 17661280 | G | A | synonymous_variant | LOW | c.1230G>A|p.Lys410Lys |
S155 S211 |
14 | BAA02g30350 | A02 | 17661970 | C | T | downstream_gene_variant | MODIFIER | c.*630C>T| |
S182 |
15 | BAA02g30350 | A02 | 17662226 | T | C | downstream_gene_variant | MODIFIER | c.*886T>C| |
S86 S98 |
16 | BAA02g30350 | A02 | 17662231 | C | T | downstream_gene_variant | MODIFIER | c.*891C>T| |
S152 |
17 | BAA02g30350 | A02 | 17663757 | G | A | downstream_gene_variant | MODIFIER | c.*2417G>A| |
S150 S172 S202 S217 |