Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g12120 | A02 | 5466234 | C | T | upstream_gene_variant | MODIFIER | c.-837C>T| |
S246 |
2 | BAA02g12120 | A02 | 5467408 | G | A | missense_variant | MODERATE | c.338G>A|p.Gly113Glu |
S205 |
3 | BAA02g12120 | A02 | 5467736 | C | T | synonymous_variant | LOW | c.666C>T|p.Cys222Cys |
S65 |
4 | BAA02g12120 | A02 | 5467861 | G | A | missense_variant | MODERATE | c.791G>A|p.Gly264Asp |
S173 S176 |
5 | BAA02g12120 | A02 | 5468084 | G | A | stop_gained | HIGH | c.1014G>A|p.Trp338* |
S206 S26 |
6 | BAA02g12120 | A02 | 5468410 | G | A | stop_gained | HIGH | c.1340G>A|p.Trp447* |
S17 |
7 | BAA02g12120 | A02 | 5468642 | G | A | missense_variant | MODERATE | c.1486G>A|p.Gly496Arg |
S176 |
8 | BAA02g12120 | A02 | 5470425 | G | A | intron_variant | MODIFIER | c.2230+162G>A| |
S2 |
9 | BAA02g12120 | A02 | 5471977 | G | A | intron_variant | MODIFIER | c.2812+285G>A| |
S188 |