Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g18350 | A10 | 17197956 | G | A | missense_variant&splice_region_variant | MODERATE | c.415G>A|p.Ala139Thr |
S157 S163 |
2 | BAA10g18350 | A10 | 17202150 | G | A | downstream_gene_variant | MODIFIER | c.*2766G>A| |
S272 |
3 | BAA10g18350 | A10 | 17203722 | C | T | downstream_gene_variant | MODIFIER | c.*4338C>T| |
S259 |
4 | BAA10g18350 | A10 | 17204092 | G | A | downstream_gene_variant | MODIFIER | c.*4708G>A| |
S7 |
5 | BAA10g18350 | A10 | 17204320 | C | T | downstream_gene_variant | MODIFIER | c.*4936C>T| |
S302 |