Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA04g00660 | A04 | 372391 | G | A | missense_variant | MODERATE | c.901G>A|p.Asp301Asn |
S246 |
2 | BAA04g00660 | A04 | 372661 | G | A | synonymous_variant | LOW | c.1056G>A|p.Leu352Leu |
S13 |
3 | BAA04g00660 | A04 | 373465 | G | A | missense_variant&splice_region_variant | MODERATE | c.1454G>A|p.Arg485Lys |
S246 |
4 | BAA04g00660 | A04 | 375557 | G | A | downstream_gene_variant | MODIFIER | c.*1506G>A| |
S217 |