Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g16930 | A10 | 16522340 | G | A | synonymous_variant | LOW | c.348C>T|p.Ser116Ser |
S113 |
2 | BAA10g16930 | A10 | 16522403 | G | A | synonymous_variant | LOW | c.285C>T|p.Thr95Thr |
S136 |
3 | BAA10g16930 | A10 | 16522435 | C | T | missense_variant | MODERATE | c.253G>A|p.Ala85Thr |
S115 |
4 | BAA10g16930 | A10 | 16525750 | C | T | upstream_gene_variant | MODIFIER | c.-2179G>A| |
S230 |
5 | BAA10g16930 | A10 | 16526547 | C | T | upstream_gene_variant | MODIFIER | c.-2976G>A| |
S186 |