Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g47860 | A02 | 38534846 | G | A | downstream_gene_variant | MODIFIER | c.*2208C>T| |
S5 |
2 | BAA02g47860 | A02 | 38534987 | C | T | downstream_gene_variant | MODIFIER | c.*2067G>A| |
S159 S243 |
3 | BAA02g47860 | A02 | 38535938 | G | A | downstream_gene_variant | MODIFIER | c.*1116C>T| |
S136 |
4 | BAA02g47860 | A02 | 38536452 | C | T | downstream_gene_variant | MODIFIER | c.*602G>A| |
S301 S304 |
5 | BAA02g47860 | A02 | 38537185 | C | T | missense_variant | MODERATE | c.2515G>A|p.Val839Met |
S13 |
6 | BAA02g47860 | A02 | 38537289 | G | A | missense_variant | MODERATE | c.2411C>T|p.Ser804Phe |
S44 |
7 | BAA02g47860 | A02 | 38539279 | G | A | missense_variant | MODERATE | c.1637C>T|p.Ser546Phe |
S36 |
8 | BAA02g47860 | A02 | 38540185 | G | A | missense_variant | MODERATE | c.1483C>T|p.Leu495Phe |
S68 |
9 | BAA02g47860 | A02 | 38540467 | C | T | intron_variant | MODIFIER | c.1319-118G>A| |
S47 |
10 | BAA02g47860 | A02 | 38540481 | C | T | intron_variant | MODIFIER | c.1319-132G>A| |
S183 S198 |
11 | BAA02g47860 | A02 | 38544521 | C | T | upstream_gene_variant | MODIFIER | c.-1101G>A| |
S133 |
12 | BAA02g47860 | A02 | 38545792 | G | A | upstream_gene_variant | MODIFIER | c.-2372C>T| |
S275 |
13 | BAA02g47860 | A02 | 38546496 | G | A | upstream_gene_variant | MODIFIER | c.-3076C>T| |
S13 |
14 | BAA02g47860 | A02 | 38547266 | C | T | upstream_gene_variant | MODIFIER | c.-3846G>A| |
S18 |
15 | BAA02g47860 | A02 | 38547301 | G | A | upstream_gene_variant | MODIFIER | c.-3881C>T| |
S50 |
16 | BAA02g47860 | A02 | 38547351 | G | A | upstream_gene_variant | MODIFIER | c.-3931C>T| |
S30 |
17 | BAA02g47860 | A02 | 38547584 | G | A | upstream_gene_variant | MODIFIER | c.-4164C>T| |
S157 S163 |
18 | BAA02g47860 | A02 | 38547871 | G | A | upstream_gene_variant | MODIFIER | c.-4451C>T| |
S162 |