Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17750 | A10 | 16946810 | G | A | upstream_gene_variant | MODIFIER | c.-3938G>A| |
S240 |
2 | BAA10g17750 | A10 | 16948256 | C | T | upstream_gene_variant | MODIFIER | c.-2492C>T| |
S26 |
3 | BAA10g17750 | A10 | 16948595 | C | T | upstream_gene_variant | MODIFIER | c.-2153C>T| |
S44 |
4 | BAA10g17750 | A10 | 16949121 | G | A | upstream_gene_variant | MODIFIER | c.-1627G>A| |
S159 S187 S188 S243 S276 S299 |
5 | BAA10g17750 | A10 | 16949167 | C | T | upstream_gene_variant | MODIFIER | c.-1581C>T| |
S12 |
6 | BAA10g17750 | A10 | 16949397 | G | A | upstream_gene_variant | MODIFIER | c.-1351G>A| |
S47 |
7 | BAA10g17750 | A10 | 16949651 | G | A | upstream_gene_variant | MODIFIER | c.-1097G>A| |
S113 |
8 | BAA10g17750 | A10 | 16950727 | C | T | upstream_gene_variant | MODIFIER | c.-21C>T| |
S301 S304 |
9 | BAA10g17750 | A10 | 16953211 | C | T | synonymous_variant | LOW | c.1707C>T|p.Asp569Asp |
S299 |
10 | BAA10g17750 | A10 | 16958158 | C | T | downstream_gene_variant | MODIFIER | c.*4932C>T| |
S48 |