Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g14960 | A09 | 8556529 | C | T | downstream_gene_variant | MODIFIER | c.*2747G>A| |
S133 |
2 | BAA09g14960 | A09 | 8559881 | G | A | missense_variant | MODERATE | c.1124C>T|p.Thr375Ile |
S225 S73 |
3 | BAA09g14960 | A09 | 8560591 | C | T | synonymous_variant | LOW | c.774G>A|p.Thr258Thr |
S303 |
4 | BAA09g14960 | A09 | 8561155 | C | T | synonymous_variant | LOW | c.501G>A|p.Val167Val |
S187 |
5 | BAA09g14960 | A09 | 8561665 | G | A | stop_gained | HIGH | c.385C>T|p.Arg129* |
S288 |
6 | BAA09g14960 | A09 | 8561877 | G | A | missense_variant | MODERATE | c.242C>T|p.Ser81Leu |
S42 |
7 | BAA09g14960 | A09 | 8562805 | C | T | upstream_gene_variant | MODIFIER | c.-687G>A| |
S23 |
8 | BAA09g14960 | A09 | 8566098 | C | T | upstream_gene_variant | MODIFIER | c.-3980G>A| |
S135 |
9 | BAA09g14960 | A09 | 8566562 | G | A | upstream_gene_variant | MODIFIER | c.-4444C>T| |
S162 |
10 | BAA09g14960 | A09 | 8566989 | C | T | upstream_gene_variant | MODIFIER | c.-4871G>A| |
S134 |