Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16200 | A05 | 8938530 | G | A | missense_variant | MODERATE | c.419C>T|p.Pro140Leu |
S240 |
2 | BAA05g16200 | A05 | 8938645 | C | T | splice_region_variant&intron_variant | LOW | c.373+4G>A| |
S114 |
3 | BAA05g16200 | A05 | 8938938 | C | T | synonymous_variant | LOW | c.84G>A|p.Gln28Gln |
S140 |
4 | BAA05g16200 | A05 | 8939317 | C | T | upstream_gene_variant | MODIFIER | c.-296G>A| |
S221 |
5 | BAA05g16200 | A05 | 8939758 | C | T | upstream_gene_variant | MODIFIER | c.-737G>A| |
S208 S93 |
6 | BAA05g16200 | A05 | 8939954 | C | A | upstream_gene_variant | MODIFIER | c.-933G>T| |
S18 S195 S246 |
7 | BAA05g16200 | A05 | 8941370 | C | T | upstream_gene_variant | MODIFIER | c.-2349G>A| |
S259 |