Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g34190 | A02 | 29301952 | C | T | upstream_gene_variant | MODIFIER | c.-4687C>T| |
S40 |
2 | BAA02g34190 | A02 | 29302189 | C | T | upstream_gene_variant | MODIFIER | c.-4450C>T| |
S162 |
3 | BAA02g34190 | A02 | 29302346 | C | T | upstream_gene_variant | MODIFIER | c.-4293C>T| |
S17 S18 |
4 | BAA02g34190 | A02 | 29303635 | G | A | upstream_gene_variant | MODIFIER | c.-3004G>A| |
S265 |
5 | BAA02g34190 | A02 | 29303637 | G | A | upstream_gene_variant | MODIFIER | c.-3002G>A| |
S306 |
6 | BAA02g34190 | A02 | 29306529 | G | A | upstream_gene_variant | MODIFIER | c.-110G>A| |
S25 |
7 | BAA02g34190 | A02 | 29306578 | C | T | upstream_gene_variant | MODIFIER | c.-61C>T| |
S79 S91 |
8 | BAA02g34190 | A02 | 29308499 | G | A | missense_variant | MODERATE | c.940G>A|p.Asp314Asn |
S57 |
9 | BAA02g34190 | A02 | 29308567 | C | T | synonymous_variant | LOW | c.1008C>T|p.Val336Val |
S308 |
10 | BAA02g34190 | A02 | 29308579 | C | T | synonymous_variant | LOW | c.1020C>T|p.Val340Val |
S182 |
11 | BAA02g34190 | A02 | 29309798 | C | T | downstream_gene_variant | MODIFIER | c.*1117C>T| |
S181 |
12 | BAA02g34190 | A02 | 29310510 | G | A | downstream_gene_variant | MODIFIER | c.*1829G>A| |
S47 |
13 | BAA02g34190 | A02 | 29310544 | C | T | downstream_gene_variant | MODIFIER | c.*1863C>T| |
S241 |