Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22200 | A01 | 11105387 | G | A | downstream_gene_variant | MODIFIER | c.*2662C>T| |
S236 |
2 | BAA01g22200 | A01 | 11108263 | G | A | missense_variant | MODERATE | c.1771C>T|p.Pro591Ser |
S238 |
3 | BAA01g22200 | A01 | 11108512 | G | A | missense_variant | MODERATE | c.1522C>T|p.Pro508Ser |
S284 |
4 | BAA01g22200 | A01 | 11109520 | C | T | synonymous_variant | LOW | c.654G>A|p.Leu218Leu |
S167 |
5 | BAA01g22200 | A01 | 11109790 | G | A | synonymous_variant | LOW | c.384C>T|p.Ile128Ile |
S235 |
6 | BAA01g22200 | A01 | 11110492 | G | A | synonymous_variant | LOW | c.118C>T|p.Leu40Leu |
S240 |
7 | BAA01g22200 | A01 | 11110918 | G | A | upstream_gene_variant | MODIFIER | c.-309C>T| |
S291 |
8 | BAA01g22200 | A01 | 11110954 | G | A | upstream_gene_variant | MODIFIER | c.-345C>T| |
S199 |
9 | BAA01g22200 | A01 | 11112219 | C | T | upstream_gene_variant | MODIFIER | c.-1610G>A| |
S210 |
10 | BAA01g22200 | A01 | 11112381 | C | T | upstream_gene_variant | MODIFIER | c.-1772G>A| |
S295 |