Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g43610 | A05 | 41003930 | G | A | upstream_gene_variant | MODIFIER | c.-1989G>A| |
S271 |
2 | BAA05g43610 | A05 | 41003958 | G | A | upstream_gene_variant | MODIFIER | c.-1961G>A| |
S250 |
3 | BAA05g43610 | A05 | 41004233 | C | T | upstream_gene_variant | MODIFIER | c.-1686C>T| |
S149 |
4 | BAA05g43610 | A05 | 41004240 | C | T | upstream_gene_variant | MODIFIER | c.-1679C>T| |
S80 |
5 | BAA05g43610 | A05 | 41004910 | C | T | upstream_gene_variant | MODIFIER | c.-1009C>T| |
S284 |
6 | BAA05g43610 | A05 | 41005487 | G | A | upstream_gene_variant | MODIFIER | c.-432G>A| |
S150 |
7 | BAA05g43610 | A05 | 41005913 | G | A | upstream_gene_variant | MODIFIER | c.-6G>A| |
S186 |
8 | BAA05g43610 | A05 | 41007318 | C | T | missense_variant | MODERATE | c.653C>T|p.Pro218Leu |
S57 |
9 | BAA05g43610 | A05 | 41007333 | G | A | missense_variant | MODERATE | c.668G>A|p.Gly223Glu |
S179 |