Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g22050 | A01 | 10997607 | G | A | missense_variant | MODERATE | c.653C>T|p.Thr218Ile |
S100 |
2 | BAA01g22050 | A01 | 10998756 | G | A | stop_gained | HIGH | c.256C>T|p.Gln86* |
S239 |
3 | BAA01g22050 | A01 | 10998943 | C | T | synonymous_variant | LOW | c.69G>A|p.Val23Val |
S266 |
4 | BAA01g22050 | A01 | 11000345 | C | T | upstream_gene_variant | MODIFIER | c.-1334G>A| |
S277 |
5 | BAA01g22050 | A01 | 11002352 | G | A | upstream_gene_variant | MODIFIER | c.-3341C>T| |
S299 |