Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g46070 | A01 | 30698715 | C | T | missense_variant | MODERATE | c.1085G>A|p.Gly362Glu |
S156 |
2 | BAA01g46070 | A01 | 30699016 | C | T | missense_variant | MODERATE | c.784G>A|p.Asp262Asn |
S54 |
3 | BAA01g46070 | A01 | 30699103 | T | C | missense_variant | MODERATE | c.697A>G|p.Lys233Glu |
S162 S210 S220 S225 S229 S234 |
4 | BAA01g46070 | A01 | 30699387 | G | A | missense_variant | MODERATE | c.413C>T|p.Ala138Val |
S265 |
5 | BAA01g46070 | A01 | 30701762 | C | T | synonymous_variant | LOW | c.195G>A|p.Glu65Glu |
S210 |
6 | BAA01g46070 | A01 | 30701925 | G | A | missense_variant | MODERATE | c.32C>T|p.Ser11Phe |
S224 |
7 | BAA01g46070 | A01 | 30701990 | G | A | upstream_gene_variant | MODIFIER | c.-34C>T| |
S185 |
8 | BAA01g46070 | A01 | 30704590 | C | T | upstream_gene_variant | MODIFIER | c.-2634G>A| |
S146 |
9 | BAA01g46070 | A01 | 30705073 | C | T | upstream_gene_variant | MODIFIER | c.-3117G>A| |
S183 S198 |
10 | BAA01g46070 | A01 | 30705309 | G | A | upstream_gene_variant | MODIFIER | c.-3353C>T| |
S157 S163 |