Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g33460 | A02 | 28644629 | C | T | missense_variant | MODERATE | c.1528G>A|p.Val510Ile |
S241 |
2 | BAA02g33460 | A02 | 28645245 | C | T | synonymous_variant | LOW | c.1011G>A|p.Lys337Lys |
S33 |
3 | BAA02g33460 | A02 | 28645733 | G | A | missense_variant | MODERATE | c.604C>T|p.His202Tyr |
S13 |
4 | BAA02g33460 | A02 | 28646332 | G | A | missense_variant | MODERATE | c.5C>T|p.Thr2Ile |
S62 |
5 | BAA02g33460 | A02 | 28646391 | C | T | upstream_gene_variant | MODIFIER | c.-55G>A| |
S15 S156 S3 S34 |
6 | BAA02g33460 | A02 | 28646479 | G | A | upstream_gene_variant | MODIFIER | c.-143C>T| |
S155 S211 |