Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g20200 | A01 | 9933063 | C | T | synonymous_variant | LOW | c.504G>A|p.Ala168Ala |
S167 |
2 | BAA01g20200 | A01 | 9933268 | G | A | missense_variant | MODERATE | c.299C>T|p.Ser100Phe |
S174 S216 S241 S39 |
3 | BAA01g20200 | A01 | 9936871 | C | T | upstream_gene_variant | MODIFIER | c.-3305G>A| |
S242 |
4 | BAA01g20200 | A01 | 9937232 | C | T | upstream_gene_variant | MODIFIER | c.-3666G>A| |
S153 |
5 | BAA01g20200 | A01 | 9937365 | G | A | upstream_gene_variant | MODIFIER | c.-3799C>T| |
S181 |
6 | BAA01g20200 | A01 | 9937780 | G | A | upstream_gene_variant | MODIFIER | c.-4214C>T| |
S93 |