Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g42770 | A01 | 28332687 | C | T | missense_variant | MODERATE | c.857G>A|p.Gly286Glu |
S164 |
2 | BAA01g42770 | A01 | 28332964 | C | T | missense_variant | MODERATE | c.647G>A|p.Arg216Lys |
S203 |
3 | BAA01g42770 | A01 | 28333575 | C | T | synonymous_variant | LOW | c.267G>A|p.Val89Val |
S112 |
4 | BAA01g42770 | A01 | 28333811 | C | T | missense_variant | MODERATE | c.31G>A|p.Ala11Thr |
S23 |
5 | BAA01g42770 | A01 | 28334172 | G | A | upstream_gene_variant | MODIFIER | c.-331C>T| |
S53 |
6 | BAA01g42770 | A01 | 28336763 | G | A | upstream_gene_variant | MODIFIER | c.-2922C>T| |
S38 |
7 | BAA01g42770 | A01 | 28338351 | C | T | upstream_gene_variant | MODIFIER | c.-4510G>A| |
S259 |