Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g41490 | A05 | 39619658 | C | T | missense_variant | MODERATE | c.427G>A|p.Gly143Arg |
S172 S217 |
2 | BAA05g41490 | A05 | 39620507 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.93-1G>A| |
S205 |
3 | BAA05g41490 | A05 | 39625176 | C | T | upstream_gene_variant | MODIFIER | c.-4477G>A| |
S203 |
4 | BAA05g41490 | A05 | 39625230 | C | T | upstream_gene_variant | MODIFIER | c.-4531G>A| |
S219 |