Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01290 | A05 | 762954 | C | T | upstream_gene_variant | MODIFIER | c.-4249C>T| |
S237 |
2 | BAA05g01290 | A05 | 763614 | C | T | upstream_gene_variant | MODIFIER | c.-3589C>T| |
S255 |
3 | BAA05g01290 | A05 | 765361 | G | A | upstream_gene_variant | MODIFIER | c.-1842G>A| |
S110 |
4 | BAA05g01290 | A05 | 766498 | C | T | upstream_gene_variant | MODIFIER | c.-705C>T| |
S160 |
5 | BAA05g01290 | A05 | 766502 | G | A | upstream_gene_variant | MODIFIER | c.-701G>A| |
S116 |
6 | BAA05g01290 | A05 | 766791 | C | T | upstream_gene_variant | MODIFIER | c.-412C>T| |
S121 |
7 | BAA05g01290 | A05 | 766822 | G | A | upstream_gene_variant | MODIFIER | c.-381G>A| |
S179 |
8 | BAA05g01290 | A05 | 767992 | C | T | synonymous_variant | LOW | c.790C>T|p.Leu264Leu |
S229 |
9 | BAA05g01290 | A05 | 768199 | C | T | missense_variant | MODERATE | c.997C>T|p.Pro333Ser |
S124 |