Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g46140 | A09 | 51042288 | G | A | synonymous_variant | LOW | c.1068C>T|p.Phe356Phe |
S283 |
2 | BAA09g46140 | A09 | 51043624 | C | T | missense_variant | MODERATE | c.668G>A|p.Arg223Lys |
S251 |
3 | BAA09g46140 | A09 | 51044383 | G | A | missense_variant | MODERATE | c.422C>T|p.Ala141Val |
S244 |
4 | BAA09g46140 | A09 | 51044623 | G | A | synonymous_variant | LOW | c.267C>T|p.Leu89Leu |
S4 |
5 | BAA09g46140 | A09 | 51044817 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.74-1G>A| |
S176 |
6 | BAA09g46140 | A09 | 51045055 | G | A | upstream_gene_variant | MODIFIER | c.-78C>T| |
S75 |
7 | BAA09g46140 | A09 | 51045263 | C | T | upstream_gene_variant | MODIFIER | c.-286G>A| |
S302 |
8 | BAA09g46140 | A09 | 51045366 | G | A | upstream_gene_variant | MODIFIER | c.-389C>T| |
S234 |
9 | BAA09g46140 | A09 | 51047544 | C | T | upstream_gene_variant | MODIFIER | c.-2567G>A| |
S19 |
10 | BAA09g46140 | A09 | 51047565 | C | T | upstream_gene_variant | MODIFIER | c.-2588G>A| |
S205 |