Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g42420 | A02 | 35341695 | C | T | missense_variant | MODERATE | c.2377G>A|p.Ala793Thr |
S244 |
2 | BAA02g42420 | A02 | 35341744 | C | T | missense_variant | MODERATE | c.2328G>A|p.Met776Ile |
S202 |
3 | BAA02g42420 | A02 | 35342203 | G | A | missense_variant | MODERATE | c.1957C>T|p.Pro653Ser |
S268 |
4 | BAA02g42420 | A02 | 35343192 | C | T | missense_variant | MODERATE | c.1451G>A|p.Arg484His |
S180 S206 S26 |
5 | BAA02g42420 | A02 | 35344226 | C | T | synonymous_variant | LOW | c.417G>A|p.Arg139Arg |
S183 S198 |
6 | BAA02g42420 | A02 | 35344475 | G | A | synonymous_variant | LOW | c.168C>T|p.Leu56Leu |
S142 |
7 | BAA02g42420 | A02 | 35344696 | G | A | upstream_gene_variant | MODIFIER | c.-54C>T| |
S5 |
8 | BAA02g42420 | A02 | 35345522 | C | T | upstream_gene_variant | MODIFIER | c.-880G>A| |
S58 |
9 | BAA02g42420 | A02 | 35345806 | G | A | upstream_gene_variant | MODIFIER | c.-1164C>T| |
S37 |
10 | BAA02g42420 | A02 | 35346250 | G | A | upstream_gene_variant | MODIFIER | c.-1608C>T| |
S245 |
11 | BAA02g42420 | A02 | 35347409 | C | T | upstream_gene_variant | MODIFIER | c.-2767G>A| |
S25 S264 |
12 | BAA02g42420 | A02 | 35347782 | G | A | upstream_gene_variant | MODIFIER | c.-3140C>T| |
S155 S211 |