Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12360 | A01 | 5817059 | G | A | missense_variant | MODERATE | c.472G>A|p.Gly158Arg |
S281 |
2 | BAA01g12360 | A01 | 5817412 | G | A | synonymous_variant | LOW | c.825G>A|p.Gln275Gln |
S157 S163 |
3 | BAA01g12360 | A01 | 5817708 | C | T | missense_variant | MODERATE | c.1028C>T|p.Ser343Leu |
S221 |
4 | BAA01g12360 | A01 | 5817818 | G | A | splice_region_variant&intron_variant | LOW | c.1062-4G>A| |
S32 |
5 | BAA01g12360 | A01 | 5817928 | G | A | missense_variant | MODERATE | c.1168G>A|p.Glu390Lys |
S142 |
6 | BAA01g12360 | A01 | 5819472 | G | A | synonymous_variant | LOW | c.2712G>A|p.Lys904Lys |
S127 |
7 | BAA01g12360 | A01 | 5819659 | G | A | missense_variant | MODERATE | c.2899G>A|p.Glu967Lys |
S187 |
8 | BAA01g12360 | A01 | 5820111 | G | T | missense_variant | MODERATE | c.3264G>T|p.Trp1088Cys |
S169 S225 S73 |
9 | BAA01g12360 | A01 | 5824484 | C | T | downstream_gene_variant | MODIFIER | c.*3683C>T| |
S65 |
10 | BAA01g12360 | A01 | 5824917 | C | T | downstream_gene_variant | MODIFIER | c.*4116C>T| |
S136 |
11 | BAA01g12360 | A01 | 5825365 | C | T | downstream_gene_variant | MODIFIER | c.*4564C>T| |
S246 |
12 | BAA01g12360 | A01 | 5825471 | C | T | downstream_gene_variant | MODIFIER | c.*4670C>T| |
S100 |
13 | BAA01g12360 | A01 | 5825685 | C | A | downstream_gene_variant | MODIFIER | c.*4884C>A| |
S83 S88 |
14 | BAA01g12360 | A01 | 5825744 | C | T | downstream_gene_variant | MODIFIER | c.*4943C>T| |
S20 |