Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19360 | A01 | 9530368 | C | T | missense_variant | MODERATE | c.2648G>A|p.Arg883Gln |
S66 |
2 | BAA01g19360 | A01 | 9532729 | G | A | synonymous_variant | LOW | c.1290C>T|p.Cys430Cys |
S263 |
3 | BAA01g19360 | A01 | 9532806 | C | T | missense_variant | MODERATE | c.1213G>A|p.Ala405Thr |
S44 |
4 | BAA01g19360 | A01 | 9533970 | G | A | stop_gained | HIGH | c.748C>T|p.Gln250* |
S217 S248 |
5 | BAA01g19360 | A01 | 9534882 | C | T | splice_region_variant&intron_variant | LOW | c.276+3G>A| |
S264 |
6 | BAA01g19360 | A01 | 9536357 | G | A | upstream_gene_variant | MODIFIER | c.-1197C>T| |
S284 |
7 | BAA01g19360 | A01 | 9536756 | C | T | upstream_gene_variant | MODIFIER | c.-1596G>A| |
S82 S92 |
8 | BAA01g19360 | A01 | 9536975 | G | A | upstream_gene_variant | MODIFIER | c.-1815C>T| |
S87 |
9 | BAA01g19360 | A01 | 9538924 | G | A | upstream_gene_variant | MODIFIER | c.-3764C>T| |
S149 |
10 | BAA01g19360 | A01 | 9540087 | G | A | upstream_gene_variant | MODIFIER | c.-4927C>T| |
S202 |