Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g38040 | A02 | 32503890 | C | T | upstream_gene_variant | MODIFIER | c.-4850C>T| |
S121 |
2 | BAA02g38040 | A02 | 32504394 | G | A | upstream_gene_variant | MODIFIER | c.-4346G>A| |
S196 |
3 | BAA02g38040 | A02 | 32504595 | C | T | upstream_gene_variant | MODIFIER | c.-4145C>T| |
S139 |
4 | BAA02g38040 | A02 | 32504663 | G | A | upstream_gene_variant | MODIFIER | c.-4077G>A| |
S159 S243 |
5 | BAA02g38040 | A02 | 32504674 | G | A | upstream_gene_variant | MODIFIER | c.-4066G>A| |
S69 |
6 | BAA02g38040 | A02 | 32506635 | C | T | upstream_gene_variant | MODIFIER | c.-2105C>T| |
S203 |
7 | BAA02g38040 | A02 | 32507724 | C | T | upstream_gene_variant | MODIFIER | c.-1016C>T| |
S178 |
8 | BAA02g38040 | A02 | 32508821 | C | T | synonymous_variant | LOW | c.82C>T|p.Leu28Leu |
S121 |
9 | BAA02g38040 | A02 | 32509699 | C | T | missense_variant | MODERATE | c.241C>T|p.Pro81Ser |
S74 |
10 | BAA02g38040 | A02 | 32510564 | G | A | missense_variant | MODERATE | c.641G>A|p.Ser214Asn |
S302 |
11 | BAA02g38040 | A02 | 32512426 | G | A | downstream_gene_variant | MODIFIER | c.*1591G>A| |
S156 |
12 | BAA02g38040 | A02 | 32513579 | G | A | downstream_gene_variant | MODIFIER | c.*2744G>A| |
S67 |