Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g10660 | A10 | 12434125 | G | A | synonymous_variant | LOW | c.72C>T|p.Leu24Leu |
S1 S90 |
2 | BAA10g10660 | A10 | 12434137 | G | A | synonymous_variant | LOW | c.60C>T|p.Tyr20Tyr |
S218 |
3 | BAA10g10660 | A10 | 12435422 | G | A | upstream_gene_variant | MODIFIER | c.-1226C>T| |
S100 |
4 | BAA10g10660 | A10 | 12435454 | G | A | upstream_gene_variant | MODIFIER | c.-1258C>T| |
S130 |
5 | BAA10g10660 | A10 | 12435565 | C | T | upstream_gene_variant | MODIFIER | c.-1369G>A| |
S40 S49 |
6 | BAA10g10660 | A10 | 12436726 | C | T | upstream_gene_variant | MODIFIER | c.-2530G>A| |
S113 |
7 | BAA10g10660 | A10 | 12436756 | C | T | upstream_gene_variant | MODIFIER | c.-2560G>A| |
S143 |
8 | BAA10g10660 | A10 | 12437117 | G | A | upstream_gene_variant | MODIFIER | c.-2921C>T| |
S230 |
9 | BAA10g10660 | A10 | 12437141 | G | A | upstream_gene_variant | MODIFIER | c.-2945C>T| |
S62 |