Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g16490 | A02 | 8051003 | C | T | upstream_gene_variant | MODIFIER | c.-4407C>T| |
S139 |
2 | BAA02g16490 | A02 | 8053323 | C | T | upstream_gene_variant | MODIFIER | c.-2087C>T| |
S9 |
3 | BAA02g16490 | A02 | 8053865 | C | T | upstream_gene_variant | MODIFIER | c.-1545C>T| |
S224 |
4 | BAA02g16490 | A02 | 8053914 | C | T | upstream_gene_variant | MODIFIER | c.-1496C>T| |
S25 |
5 | BAA02g16490 | A02 | 8053940 | G | A | upstream_gene_variant | MODIFIER | c.-1470G>A| |
S144 |
6 | BAA02g16490 | A02 | 8055315 | C | T | upstream_gene_variant | MODIFIER | c.-95C>T| |
S77 |
7 | BAA02g16490 | A02 | 8055404 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S149 |
8 | BAA02g16490 | A02 | 8055425 | G | A | missense_variant | MODERATE | c.16G>A|p.Glu6Lys |
S197 |
9 | BAA02g16490 | A02 | 8055912 | G | A | downstream_gene_variant | MODIFIER | c.*19G>A| |
S247 |
10 | BAA02g16490 | A02 | 8056156 | C | T | downstream_gene_variant | MODIFIER | c.*263C>T| |
S249 |
11 | BAA02g16490 | A02 | 8056288 | G | A | downstream_gene_variant | MODIFIER | c.*395G>A| |
S210 S225 |
12 | BAA02g16490 | A02 | 8056421 | G | A | downstream_gene_variant | MODIFIER | c.*528G>A| |
S113 |
13 | BAA02g16490 | A02 | 8057817 | C | T | downstream_gene_variant | MODIFIER | c.*1924C>T| |
S18 |
14 | BAA02g16490 | A02 | 8058517 | T | C | downstream_gene_variant | MODIFIER | c.*2624T>C| |
S150 |
15 | BAA02g16490 | A02 | 8059760 | C | T | downstream_gene_variant | MODIFIER | c.*3867C>T| |
S94 |
16 | BAA02g16490 | A02 | 8059781 | C | T | downstream_gene_variant | MODIFIER | c.*3888C>T| |
S281 |
17 | BAA02g16490 | A02 | 8060121 | C | T | downstream_gene_variant | MODIFIER | c.*4228C>T| |
S156 S34 |
18 | BAA02g16490 | A02 | 8060891 | C | T | downstream_gene_variant | MODIFIER | c.*4998C>T| |
S15 S3 |