Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g06600 | A02 | 2811069 | C | T | missense_variant | MODERATE | c.5947G>A|p.Gly1983Ser |
S37 |
2 | BAA02g06600 | A02 | 2812332 | G | A | missense_variant | MODERATE | c.4684C>T|p.Leu1562Phe |
S294 |
3 | BAA02g06600 | A02 | 2812344 | C | T | missense_variant | MODERATE | c.4672G>A|p.Ala1558Thr |
S32 |
4 | BAA02g06600 | A02 | 2814363 | C | T | missense_variant | MODERATE | c.2827G>A|p.Ala943Thr |
S174 |
5 | BAA02g06600 | A02 | 2815283 | G | A | missense_variant | MODERATE | c.2404C>T|p.Pro802Ser |
S269 |
6 | BAA02g06600 | A02 | 2816923 | G | A | missense_variant | MODERATE | c.1439C>T|p.Thr480Ile |
S292 S9 |
7 | BAA02g06600 | A02 | 2817847 | C | T | stop_gained | HIGH | c.845G>A|p.Trp282* |
S203 |
8 | BAA02g06600 | A02 | 2817870 | G | A | synonymous_variant | LOW | c.822C>T|p.Arg274Arg |
S59 |
9 | BAA02g06600 | A02 | 2818400 | G | A | missense_variant | MODERATE | c.481C>T|p.Arg161Cys |
S302 |
10 | BAA02g06600 | A02 | 2821477 | G | A | upstream_gene_variant | MODIFIER | c.-2058C>T| |
S174 |
11 | BAA02g06600 | A02 | 2822536 | C | T | upstream_gene_variant | MODIFIER | c.-3117G>A| |
S207 |