Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41130 | A09 | 47950907 | C | T | missense_variant | MODERATE | c.1222G>A|p.Glu408Lys |
S92 |
2 | BAA09g41130 | A09 | 47952132 | C | T | synonymous_variant | LOW | c.894G>A|p.Arg298Arg |
S296 |
3 | BAA09g41130 | A09 | 47952488 | C | T | missense_variant | MODERATE | c.613G>A|p.Glu205Lys |
S30 S31 |
4 | BAA09g41130 | A09 | 47952554 | G | A | missense_variant | MODERATE | c.547C>T|p.Pro183Ser |
S88 |
5 | BAA09g41130 | A09 | 47953183 | T | A | upstream_gene_variant | MODIFIER | c.-83A>T| |
S95 |
6 | BAA09g41130 | A09 | 47953872 | G | A | upstream_gene_variant | MODIFIER | c.-772C>T| |
S46 |
7 | BAA09g41130 | A09 | 47953987 | C | T | upstream_gene_variant | MODIFIER | c.-887G>A| |
S30 S31 |
8 | BAA09g41130 | A09 | 47954240 | C | T | upstream_gene_variant | MODIFIER | c.-1140G>A| |
S82 |
9 | BAA09g41130 | A09 | 47954482 | G | A | upstream_gene_variant | MODIFIER | c.-1382C>T| |
S34 |
10 | BAA09g41130 | A09 | 47954911 | G | A | upstream_gene_variant | MODIFIER | c.-1811C>T| |
S218 |
11 | BAA09g41130 | A09 | 47957177 | G | A | upstream_gene_variant | MODIFIER | c.-4077C>T| |
S67 |
12 | BAA09g41130 | A09 | 47957572 | C | T | upstream_gene_variant | MODIFIER | c.-4472G>A| |
S188 |
13 | BAA09g41130 | A09 | 47957706 | C | T | upstream_gene_variant | MODIFIER | c.-4606G>A| |
S260 |