Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g19390 | A01 | 9542017 | C | T | missense_variant | MODERATE | c.1562G>A|p.Gly521Glu |
S215 |
2 | BAA01g19390 | A01 | 9544503 | C | T | upstream_gene_variant | MODIFIER | c.-290G>A| |
S270 |
3 | BAA01g19390 | A01 | 9544876 | T | A | upstream_gene_variant | MODIFIER | c.-663A>T| |
S278 |
4 | BAA01g19390 | A01 | 9544977 | C | T | upstream_gene_variant | MODIFIER | c.-764G>A| |
S218 |
5 | BAA01g19390 | A01 | 9546100 | C | T | upstream_gene_variant | MODIFIER | c.-1887G>A| |
S16 |
6 | BAA01g19390 | A01 | 9546123 | C | T | upstream_gene_variant | MODIFIER | c.-1910G>A| |
S148 S30 S31 |
7 | BAA01g19390 | A01 | 9547137 | C | T | upstream_gene_variant | MODIFIER | c.-2924G>A| |
S164 S256 |
8 | BAA01g19390 | A01 | 9548565 | C | T | upstream_gene_variant | MODIFIER | c.-4352G>A| |
S176 |
9 | BAA01g19390 | A01 | 9548619 | C | T | upstream_gene_variant | MODIFIER | c.-4406G>A| |
S18 |
10 | BAA01g19390 | A01 | 9549080 | G | A | upstream_gene_variant | MODIFIER | c.-4867C>T| |
S138 |