Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g00600 | A09 | 564597 | C | T | synonymous_variant | LOW | c.924G>A|p.Leu308Leu |
S261 |
2 | BAA09g00600 | A09 | 565188 | G | A | synonymous_variant | LOW | c.333C>T|p.Phe111Phe |
S296 |
3 | BAA09g00600 | A09 | 565405 | C | T | missense_variant | MODERATE | c.116G>A|p.Arg39Lys |
S215 |
4 | BAA09g00600 | A09 | 566036 | C | T | upstream_gene_variant | MODIFIER | c.-516G>A| |
S39 |
5 | BAA09g00600 | A09 | 568282 | C | T | upstream_gene_variant | MODIFIER | c.-2762G>A| |
S19 |
6 | BAA09g00600 | A09 | 569222 | C | T | upstream_gene_variant | MODIFIER | c.-3702G>A| |
S156 S34 S4 S6 |
7 | BAA09g00600 | A09 | 569825 | C | T | upstream_gene_variant | MODIFIER | c.-4305G>A| |
S134 |
8 | BAA09g00600 | A09 | 570032 | C | T | upstream_gene_variant | MODIFIER | c.-4512G>A| |
S156 |
9 | BAA09g00600 | A09 | 570052 | G | A | upstream_gene_variant | MODIFIER | c.-4532C>T| |
S112 |
10 | BAA09g00600 | A09 | 570373 | C | T | upstream_gene_variant | MODIFIER | c.-4853G>A| |
S56 |