Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA08g01080 | A08 | 777777 | C | T | upstream_gene_variant | MODIFIER | c.-4478C>T| |
S113 |
2 | BAA08g01080 | A08 | 777914 | G | A | upstream_gene_variant | MODIFIER | c.-4341G>A| |
S94 |
3 | BAA08g01080 | A08 | 782612 | G | A | missense_variant | MODERATE | c.76G>A|p.Val26Met |
S282 |
4 | BAA08g01080 | A08 | 784297 | C | T | synonymous_variant | LOW | c.810C>T|p.Asn270Asn |
S153 S213 |
5 | BAA08g01080 | A08 | 786809 | C | T | downstream_gene_variant | MODIFIER | c.*2199C>T| |
S135 |
6 | BAA08g01080 | A08 | 788941 | C | T | downstream_gene_variant | MODIFIER | c.*4331C>T| |
S135 |
7 | BAA08g01080 | A08 | 789059 | G | A | downstream_gene_variant | MODIFIER | c.*4449G>A| |
S242 |