Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g19630 | A02 | 10206916 | C | T | downstream_gene_variant | MODIFIER | c.*3021G>A| |
S171 |
2 | BAA02g19630 | A02 | 10210296 | C | T | missense_variant | MODERATE | c.1648G>A|p.Glu550Lys |
S219 S72 |
3 | BAA02g19630 | A02 | 10210328 | G | A | missense_variant | MODERATE | c.1616C>T|p.Ser539Phe |
S167 S236 S262 S263 |
4 | BAA02g19630 | A02 | 10210570 | C | T | stop_gained | HIGH | c.1374G>A|p.Trp458* |
S105 |
5 | BAA02g19630 | A02 | 10212302 | C | T | missense_variant | MODERATE | c.934G>A|p.Gly312Arg |
S281 |
6 | BAA02g19630 | A02 | 10212416 | C | T | missense_variant | MODERATE | c.820G>A|p.Val274Ile |
S302 |
7 | BAA02g19630 | A02 | 10213084 | G | A | missense_variant | MODERATE | c.152C>T|p.Ser51Leu |
S245 |
8 | BAA02g19630 | A02 | 10214259 | G | A | upstream_gene_variant | MODIFIER | c.-1024C>T| |
S166 |
9 | BAA02g19630 | A02 | 10214374 | C | T | upstream_gene_variant | MODIFIER | c.-1139G>A| |
S224 |
10 | BAA02g19630 | A02 | 10217505 | C | T | upstream_gene_variant | MODIFIER | c.-4270G>A| |
S28 |
11 | BAA02g19630 | A02 | 10217822 | G | A | upstream_gene_variant | MODIFIER | c.-4587C>T| |
S170 |