Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g13450 | A10 | 14523141 | G | A | synonymous_variant | LOW | c.546C>T|p.Ser182Ser |
S139 |
2 | BAA10g13450 | A10 | 14523271 | C | T | missense_variant | MODERATE | c.416G>A|p.Cys139Tyr |
S275 |
3 | BAA10g13450 | A10 | 14523639 | G | A | synonymous_variant | LOW | c.48C>T|p.Ala16Ala |
S158 |
4 | BAA10g13450 | A10 | 14528028 | C | T | upstream_gene_variant | MODIFIER | c.-4342G>A| |
S281 |
5 | BAA10g13450 | A10 | 14528361 | G | A | upstream_gene_variant | MODIFIER | c.-4675C>T| |
S169 |