Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41530 | A01 | 27576962 | G | A | missense_variant | MODERATE | c.139G>A|p.Glu47Lys |
S259 |
2 | BAA01g41530 | A01 | 27577072 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.178-1G>A| |
S155 |
3 | BAA01g41530 | A01 | 27577093 | G | A | synonymous_variant | LOW | c.198G>A|p.Gln66Gln |
S45 |
4 | BAA01g41530 | A01 | 27577115 | G | A | missense_variant | MODERATE | c.220G>A|p.Glu74Lys |
S149 |
5 | BAA01g41530 | A01 | 27579018 | C | T | missense_variant | MODERATE | c.1378C>T|p.Pro460Ser |
S198 |
6 | BAA01g41530 | A01 | 27579667 | C | T | missense_variant | MODERATE | c.1790C>T|p.Ala597Val |
S168 |
7 | BAA01g41530 | A01 | 27581790 | C | T | downstream_gene_variant | MODIFIER | c.*1981C>T| |
S74 |
8 | BAA01g41530 | A01 | 27582336 | C | T | downstream_gene_variant | MODIFIER | c.*2527C>T| |
S277 |