Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g09790 | A02 | 4315021 | G | A | intron_variant | MODIFIER | c.2237+114C>T| |
S79 S91 |
2 | BAA02g09790 | A02 | 4316206 | C | T | missense_variant | MODERATE | c.1657G>A|p.Gly553Arg |
S167 |
3 | BAA02g09790 | A02 | 4316544 | G | A | intron_variant | MODIFIER | c.1638+86C>T| |
S45 |
4 | BAA02g09790 | A02 | 4316840 | C | T | synonymous_variant | LOW | c.1428G>A|p.Arg476Arg |
S200 |
5 | BAA02g09790 | A02 | 4317220 | G | A | intron_variant | MODIFIER | c.1286+57C>T| |
S291 |
6 | BAA02g09790 | A02 | 4317316 | G | A | missense_variant | MODERATE | c.1247C>T|p.Ala416Val |
S50 |
7 | BAA02g09790 | A02 | 4318287 | C | T | intron_variant | MODIFIER | c.738-80G>A| |
S117 |
8 | BAA02g09790 | A02 | 4319348 | C | T | splice_donor_variant&intron_variant | HIGH | c.268+1G>A| |
S230 |
9 | BAA02g09790 | A02 | 4320067 | C | T | upstream_gene_variant | MODIFIER | c.-372G>A| |
S261 |