Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g03300 | A02 | 1459938 | G | A | downstream_gene_variant | MODIFIER | c.*3762C>T| |
S228 |
2 | BAA02g03300 | A02 | 1460155 | C | T | downstream_gene_variant | MODIFIER | c.*3545G>A| |
S306 |
3 | BAA02g03300 | A02 | 1460162 | G | A | downstream_gene_variant | MODIFIER | c.*3538C>T| |
S68 |
4 | BAA02g03300 | A02 | 1460211 | G | A | downstream_gene_variant | MODIFIER | c.*3489C>T| |
S134 |
5 | BAA02g03300 | A02 | 1460311 | C | T | downstream_gene_variant | MODIFIER | c.*3389G>A| |
S239 |
6 | BAA02g03300 | A02 | 1460531 | C | T | downstream_gene_variant | MODIFIER | c.*3169G>A| |
S298 |
7 | BAA02g03300 | A02 | 1462129 | G | A | downstream_gene_variant | MODIFIER | c.*1571C>T| |
S249 |
8 | BAA02g03300 | A02 | 1464162 | G | T | splice_region_variant&intron_variant | LOW | c.820-3C>A| |
S64 |
9 | BAA02g03300 | A02 | 1464482 | G | A | synonymous_variant | LOW | c.675C>T|p.Val225Val |
S148 S210 S30 S31 |
10 | BAA02g03300 | A02 | 1465288 | G | A | missense_variant | MODERATE | c.250C>T|p.Pro84Ser |
S156 |
11 | BAA02g03300 | A02 | 1465389 | G | A | missense_variant | MODERATE | c.149C>T|p.Ala50Val |
S210 |
12 | BAA02g03300 | A02 | 1468743 | C | T | upstream_gene_variant | MODIFIER | c.-3076G>A| |
S292 |
13 | BAA02g03300 | A02 | 1470143 | G | A | upstream_gene_variant | MODIFIER | c.-4476C>T| |
S36 |
14 | BAA02g03300 | A02 | 1470483 | C | A | upstream_gene_variant | MODIFIER | c.-4816G>T| |
S126 |
15 | BAA02g03300 | A02 | 1470569 | C | T | upstream_gene_variant | MODIFIER | c.-4902G>A| |
S34 |