Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g41600 | A09 | 48283482 | C | T | missense_variant | MODERATE | c.3284G>A|p.Gly1095Asp |
S133 |
2 | BAA09g41600 | A09 | 48283799 | C | T | synonymous_variant | LOW | c.2967G>A|p.Glu989Glu |
S20 |
3 | BAA09g41600 | A09 | 48284246 | G | A | missense_variant | MODERATE | c.2680C>T|p.Leu894Phe |
S247 |
4 | BAA09g41600 | A09 | 48284248 | G | A | missense_variant | MODERATE | c.2678C>T|p.Ser893Phe |
S216 |
5 | BAA09g41600 | A09 | 48284271 | C | T | synonymous_variant | LOW | c.2655G>A|p.Glu885Glu |
S302 |
6 | BAA09g41600 | A09 | 48285461 | C | T | synonymous_variant | LOW | c.1707G>A|p.Thr569Thr |
S245 |
7 | BAA09g41600 | A09 | 48285481 | C | T | missense_variant | MODERATE | c.1687G>A|p.Glu563Lys |
S94 |
8 | BAA09g41600 | A09 | 48286031 | C | T | synonymous_variant | LOW | c.1137G>A|p.Thr379Thr |
S209 |
9 | BAA09g41600 | A09 | 48286226 | C | T | synonymous_variant | LOW | c.942G>A|p.Glu314Glu |
S229 |
10 | BAA09g41600 | A09 | 48286740 | G | A | missense_variant | MODERATE | c.565C>T|p.Arg189Cys |
S85 |
11 | BAA09g41600 | A09 | 48286843 | C | T | synonymous_variant | LOW | c.462G>A|p.Arg154Arg |
S100 |
12 | BAA09g41600 | A09 | 48288326 | G | A | upstream_gene_variant | MODIFIER | c.-872C>T| |
S23 |
13 | BAA09g41600 | A09 | 48288736 | G | A | upstream_gene_variant | MODIFIER | c.-1282C>T| |
S195 S277 |
14 | BAA09g41600 | A09 | 48289140 | C | T | upstream_gene_variant | MODIFIER | c.-1686G>A| |
S159 S243 S299 |