Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44240 | A09 | 50015868 | C | T | synonymous_variant | LOW | c.159C>T|p.Asn53Asn |
S130 S32 |
2 | BAA09g44240 | A09 | 50015966 | G | A | missense_variant | MODERATE | c.257G>A|p.Gly86Asp |
S82 |
3 | BAA09g44240 | A09 | 50015971 | G | A | missense_variant | MODERATE | c.262G>A|p.Val88Ile |
S265 |
4 | BAA09g44240 | A09 | 50020996 | C | T | downstream_gene_variant | MODIFIER | c.*3947C>T| |
S28 |
5 | BAA09g44240 | A09 | 50021179 | C | T | downstream_gene_variant | MODIFIER | c.*4130C>T| |
S302 |
6 | BAA09g44240 | A09 | 50021935 | G | A | downstream_gene_variant | MODIFIER | c.*4886G>A| |
S116 |
7 | BAA09g44240 | A09 | 50021978 | G | A | downstream_gene_variant | MODIFIER | c.*4929G>A| |
S45 |
8 | BAA09g44240 | A09 | 50022038 | C | T | downstream_gene_variant | MODIFIER | c.*4989C>T| |
S122 |