Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g64940 | A09 | 60054482 | C | T | missense_variant | MODERATE | c.865G>A|p.Ala289Thr |
S120 |
2 | BAA09g64940 | A09 | 60054706 | G | A | synonymous_variant | LOW | c.729C>T|p.Ala243Ala |
S231 |
3 | BAA09g64940 | A09 | 60055556 | C | T | splice_region_variant&intron_variant | LOW | c.298-6G>A| |
S37 |
4 | BAA09g64940 | A09 | 60060749 | C | T | upstream_gene_variant | MODIFIER | c.-4472G>A| |
S109 |