Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32880 | A02 | 28141899 | C | T | downstream_gene_variant | MODIFIER | c.*2262G>A| |
S2 |
2 | BAA02g32880 | A02 | 28142811 | G | A | downstream_gene_variant | MODIFIER | c.*1350C>T| |
S297 |
3 | BAA02g32880 | A02 | 28145073 | C | T | synonymous_variant | LOW | c.2088G>A|p.Lys696Lys |
S109 |
4 | BAA02g32880 | A02 | 28145556 | G | A | missense_variant&splice_region_variant | MODERATE | c.1781C>T|p.Ser594Phe |
S148 S30 S31 |
5 | BAA02g32880 | A02 | 28146342 | C | T | synonymous_variant | LOW | c.1155G>A|p.Glu385Glu |
S201 |
6 | BAA02g32880 | A02 | 28146378 | C | T | synonymous_variant | LOW | c.1119G>A|p.Glu373Glu |
S6 |
7 | BAA02g32880 | A02 | 28146702 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.913-1G>A| |
S165 |
8 | BAA02g32880 | A02 | 28147171 | C | T | missense_variant | MODERATE | c.680G>A|p.Arg227His |
S64 |
9 | BAA02g32880 | A02 | 28147418 | C | T | missense_variant | MODERATE | c.433G>A|p.Asp145Asn |
S18 |
10 | BAA02g32880 | A02 | 28147841 | C | T | missense_variant | MODERATE | c.10G>A|p.Glu4Lys |
S117 |
11 | BAA02g32880 | A02 | 28148623 | G | A | upstream_gene_variant | MODIFIER | c.-773C>T| |
S224 |
12 | BAA02g32880 | A02 | 28151384 | G | A | upstream_gene_variant | MODIFIER | c.-3534C>T| |
S210 S225 |
13 | BAA02g32880 | A02 | 28151496 | G | A | upstream_gene_variant | MODIFIER | c.-3646C>T| |
S235 |