Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g00920 | A01 | 401079 | C | T | synonymous_variant | LOW | c.99C>T|p.Phe33Phe |
S132 S137 S215 |
2 | BAA01g00920 | A01 | 401460 | C | T | missense_variant | MODERATE | c.389C>T|p.Thr130Ile |
S126 |
3 | BAA01g00920 | A01 | 401573 | G | A | missense_variant | MODERATE | c.502G>A|p.Asp168Asn |
S162 |
4 | BAA01g00920 | A01 | 406574 | G | A | downstream_gene_variant | MODIFIER | c.*4038G>A| |
S295 |
5 | BAA01g00920 | A01 | 406907 | G | A | downstream_gene_variant | MODIFIER | c.*4371G>A| |
S134 S193 |
6 | BAA01g00920 | A01 | 407305 | C | T | downstream_gene_variant | MODIFIER | c.*4769C>T| |
S59 |