Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g20420 | A02 | 10842362 | G | A | stop_gained | HIGH | c.399G>A|p.Trp133* |
S172 S217 |
2 | BAA02g20420 | A02 | 10842389 | G | A | splice_region_variant&synonymous_variant | LOW | c.426G>A|p.Glu142Glu |
S134 |
3 | BAA02g20420 | A02 | 10842410 | C | T | intron_variant | MODIFIER | c.426+21C>T| |
S38 |
4 | BAA02g20420 | A02 | 10842493 | C | T | synonymous_variant | LOW | c.456C>T|p.Asp152Asp |
S131 |
5 | BAA02g20420 | A02 | 10842734 | G | A | missense_variant | MODERATE | c.589G>A|p.Ala197Thr |
S28 |
6 | BAA02g20420 | A02 | 10845551 | C | T | synonymous_variant | LOW | c.1251C>T|p.Pro417Pro |
S206 |
7 | BAA02g20420 | A02 | 10847360 | C | T | downstream_gene_variant | MODIFIER | c.*1201C>T| |
S5 |
8 | BAA02g20420 | A02 | 10848149 | C | T | downstream_gene_variant | MODIFIER | c.*1990C>T| |
S301 S304 |
9 | BAA02g20420 | A02 | 10848345 | C | T | downstream_gene_variant | MODIFIER | c.*2186C>T| |
S249 |