Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g44140 | A01 | 29273818 | G | A | synonymous_variant | LOW | c.2586C>T|p.Val862Val |
S274 |
2 | BAA01g44140 | A01 | 29274129 | C | T | missense_variant | MODERATE | c.2275G>A|p.Val759Met |
S259 |
3 | BAA01g44140 | A01 | 29274199 | C | T | synonymous_variant | LOW | c.2205G>A|p.Arg735Arg |
S11 |
4 | BAA01g44140 | A01 | 29274281 | G | A | missense_variant | MODERATE | c.2123C>T|p.Ser708Phe |
S250 |
5 | BAA01g44140 | A01 | 29275513 | C | T | missense_variant | MODERATE | c.1255G>A|p.Asp419Asn |
S204 S59 |
6 | BAA01g44140 | A01 | 29276331 | C | A | missense_variant | MODERATE | c.654G>T|p.Met218Ile |
S56 |
7 | BAA01g44140 | A01 | 29276496 | C | T | synonymous_variant | LOW | c.489G>A|p.Leu163Leu |
S234 |
8 | BAA01g44140 | A01 | 29278063 | C | T | upstream_gene_variant | MODIFIER | c.-1079G>A| |
S28 |
9 | BAA01g44140 | A01 | 29280004 | C | T | upstream_gene_variant | MODIFIER | c.-3020G>A| |
S68 |
10 | BAA01g44140 | A01 | 29281010 | G | A | upstream_gene_variant | MODIFIER | c.-4026C>T| |
S123 |
11 | BAA01g44140 | A01 | 29281773 | C | T | upstream_gene_variant | MODIFIER | c.-4789G>A| |
S41 |