Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26620 | A05 | 31231915 | C | T | upstream_gene_variant | MODIFIER | c.-4875C>T| |
S124 S127 S128 S131 S190 S255 S284 S287 S58 |
2 | BAA05g26620 | A05 | 31232852 | C | T | upstream_gene_variant | MODIFIER | c.-3938C>T| |
S55 |
3 | BAA05g26620 | A05 | 31233518 | G | A | upstream_gene_variant | MODIFIER | c.-3272G>A| |
S23 |
4 | BAA05g26620 | A05 | 31234436 | G | A | upstream_gene_variant | MODIFIER | c.-2354G>A| |
S259 |
5 | BAA05g26620 | A05 | 31234943 | G | A | upstream_gene_variant | MODIFIER | c.-1847G>A| |
S186 |
6 | BAA05g26620 | A05 | 31236981 | C | T | missense_variant | MODERATE | c.103C>T|p.Pro35Ser |
S172 S217 |
7 | BAA05g26620 | A05 | 31238864 | G | A | missense_variant | MODERATE | c.868G>A|p.Ala290Thr |
S122 |
8 | BAA05g26620 | A05 | 31239333 | C | T | synonymous_variant | LOW | c.1116C>T|p.Pro372Pro |
S288 |
9 | BAA05g26620 | A05 | 31244886 | C | T | downstream_gene_variant | MODIFIER | c.*3765C>T| |
S237 |