Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g61880 | A09 | 58678631 | C | T | synonymous_variant | LOW | c.384C>T|p.Leu128Leu |
S233 |
2 | BAA09g61880 | A09 | 58678686 | C | T | missense_variant | MODERATE | c.439C>T|p.Arg147Trp |
S96 |
3 | BAA09g61880 | A09 | 58680776 | C | T | missense_variant | MODERATE | c.1792C>T|p.Pro598Ser |
S152 |
4 | BAA09g61880 | A09 | 58681684 | C | T | stop_gained | HIGH | c.2164C>T|p.Gln722* |
S26 |
5 | BAA09g61880 | A09 | 58681718 | G | A | missense_variant | MODERATE | c.2198G>A|p.Ser733Asn |
S19 |
6 | BAA09g61880 | A09 | 58681754 | C | T | missense_variant | MODERATE | c.2234C>T|p.Ala745Val |
S245 |
7 | BAA09g61880 | A09 | 58682676 | G | A | downstream_gene_variant | MODIFIER | c.*585G>A| |
S148 S30 S31 |
8 | BAA09g61880 | A09 | 58682701 | C | T | downstream_gene_variant | MODIFIER | c.*610C>T| |
S103 |
9 | BAA09g61880 | A09 | 58683704 | A | G | downstream_gene_variant | MODIFIER | c.*1613A>G| |
S11 |
10 | BAA09g61880 | A09 | 58683982 | C | T | downstream_gene_variant | MODIFIER | c.*1891C>T| |
S120 |
11 | BAA09g61880 | A09 | 58684827 | C | T | downstream_gene_variant | MODIFIER | c.*2736C>T| |
S96 |