Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA09g44790 | A09 | 50285363 | G | A | upstream_gene_variant | MODIFIER | c.-1851G>A| |
S47 |
2 | BAA09g44790 | A09 | 50287339 | C | T | synonymous_variant | LOW | c.126C>T|p.Arg42Arg |
S99 |
3 | BAA09g44790 | A09 | 50287393 | C | T | synonymous_variant | LOW | c.180C>T|p.Asn60Asn |
S5 |
4 | BAA09g44790 | A09 | 50287405 | C | T | synonymous_variant | LOW | c.192C>T|p.Arg64Arg |
S159 S243 S299 |
5 | BAA09g44790 | A09 | 50287407 | G | A | missense_variant | MODERATE | c.194G>A|p.Gly65Glu |
S270 |
6 | BAA09g44790 | A09 | 50287411 | C | T | synonymous_variant | LOW | c.198C>T|p.Ser66Ser |
S192 |
7 | BAA09g44790 | A09 | 50287443 | C | T | missense_variant | MODERATE | c.230C>T|p.Ser77Phe |
S303 |
8 | BAA09g44790 | A09 | 50287723 | C | T | synonymous_variant | LOW | c.510C>T|p.Leu170Leu |
S180 |
9 | BAA09g44790 | A09 | 50287757 | G | A | missense_variant | MODERATE | c.544G>A|p.Asp182Asn |
S2 |
10 | BAA09g44790 | A09 | 50287798 | C | T | synonymous_variant | LOW | c.585C>T|p.Asn195Asn |
S92 |
11 | BAA09g44790 | A09 | 50288164 | G | A | synonymous_variant | LOW | c.951G>A|p.Pro317Pro |
S54 |