Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g40060 | A02 | 33855057 | C | T | downstream_gene_variant | MODIFIER | c.*3843G>A| |
S171 |
2 | BAA02g40060 | A02 | 33855752 | C | T | downstream_gene_variant | MODIFIER | c.*3148G>A| |
S266 |
3 | BAA02g40060 | A02 | 33856261 | C | T | downstream_gene_variant | MODIFIER | c.*2639G>A| |
S152 |
4 | BAA02g40060 | A02 | 33858952 | G | A | missense_variant | MODERATE | c.686C>T|p.Ala229Val |
S288 |
5 | BAA02g40060 | A02 | 33861373 | G | A | upstream_gene_variant | MODIFIER | c.-712C>T| |
S176 |
6 | BAA02g40060 | A02 | 33861417 | C | T | upstream_gene_variant | MODIFIER | c.-756G>A| |
S203 |
7 | BAA02g40060 | A02 | 33861659 | C | T | upstream_gene_variant | MODIFIER | c.-998G>A| |
S79 |
8 | BAA02g40060 | A02 | 33862127 | G | A | upstream_gene_variant | MODIFIER | c.-1466C>T| |
S122 |
9 | BAA02g40060 | A02 | 33862553 | G | A | upstream_gene_variant | MODIFIER | c.-1892C>T| |
S217 S248 |
10 | BAA02g40060 | A02 | 33862659 | C | T | upstream_gene_variant | MODIFIER | c.-1998G>A| |
S140 |
11 | BAA02g40060 | A02 | 33862672 | C | T | upstream_gene_variant | MODIFIER | c.-2011G>A| |
S56 |
12 | BAA02g40060 | A02 | 33862727 | C | T | upstream_gene_variant | MODIFIER | c.-2066G>A| |
S301 S304 |
13 | BAA02g40060 | A02 | 33863233 | C | T | upstream_gene_variant | MODIFIER | c.-2572G>A| |
S255 |
14 | BAA02g40060 | A02 | 33863804 | G | A | upstream_gene_variant | MODIFIER | c.-3143C>T| |
S155 S211 |
15 | BAA02g40060 | A02 | 33865029 | C | T | upstream_gene_variant | MODIFIER | c.-4368G>A| |
S263 |