Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g10920 | A02 | 4890496 | G | A | upstream_gene_variant | MODIFIER | c.-3661G>A| |
S4 |
2 | BAA02g10920 | A02 | 4890839 | C | T | upstream_gene_variant | MODIFIER | c.-3318C>T| |
S152 |
3 | BAA02g10920 | A02 | 4890865 | C | T | upstream_gene_variant | MODIFIER | c.-3292C>T| |
S306 |
4 | BAA02g10920 | A02 | 4890894 | G | A | upstream_gene_variant | MODIFIER | c.-3263G>A| |
S173 |
5 | BAA02g10920 | A02 | 4890900 | G | A | upstream_gene_variant | MODIFIER | c.-3257G>A| |
S110 |
6 | BAA02g10920 | A02 | 4890929 | G | A | upstream_gene_variant | MODIFIER | c.-3228G>A| |
S144 |
7 | BAA02g10920 | A02 | 4891363 | C | T | upstream_gene_variant | MODIFIER | c.-2794C>T| |
S54 |
8 | BAA02g10920 | A02 | 4892671 | G | A | upstream_gene_variant | MODIFIER | c.-1486G>A| |
S35 |
9 | BAA02g10920 | A02 | 4892707 | C | T | upstream_gene_variant | MODIFIER | c.-1450C>T| |
S5 |
10 | BAA02g10920 | A02 | 4893606 | C | T | upstream_gene_variant | MODIFIER | c.-551C>T| |
S183 S198 |
11 | BAA02g10920 | A02 | 4893972 | C | T | upstream_gene_variant | MODIFIER | c.-185C>T| |
S64 |
12 | BAA02g10920 | A02 | 4894594 | C | T | synonymous_variant | LOW | c.438C>T|p.Ser146Ser |
S185 |
13 | BAA02g10920 | A02 | 4894606 | C | T | synonymous_variant | LOW | c.450C>T|p.Asp150Asp |
S175 |
14 | BAA02g10920 | A02 | 4894626 | C | T | missense_variant | MODERATE | c.470C>T|p.Ser157Phe |
S118 |
15 | BAA02g10920 | A02 | 4894862 | G | A | missense_variant | MODERATE | c.706G>A|p.Gly236Arg |
S303 |
16 | BAA02g10920 | A02 | 4895188 | C | T | synonymous_variant | LOW | c.1032C>T|p.Phe344Phe |
S183 S198 |
17 | BAA02g10920 | A02 | 4898034 | C | T | missense_variant | MODERATE | c.2437C>T|p.Leu813Phe |
S156 S34 |