Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g34760 | A05 | 35788303 | G | A | missense_variant | MODERATE | c.292G>A|p.Glu98Lys |
S9 |
2 | BAA05g34760 | A05 | 35788696 | C | T | missense_variant | MODERATE | c.352C>T|p.Pro118Ser |
S140 |
3 | BAA05g34760 | A05 | 35790282 | G | A | missense_variant | MODERATE | c.1460G>A|p.Gly487Glu |
S179 |
4 | BAA05g34760 | A05 | 35790617 | G | A | missense_variant | MODERATE | c.1795G>A|p.Glu599Lys |
S116 |
5 | BAA05g34760 | A05 | 35790698 | C | T | missense_variant | MODERATE | c.1876C>T|p.Pro626Ser |
S174 |
6 | BAA05g34760 | A05 | 35790722 | G | A | missense_variant | MODERATE | c.1900G>A|p.Glu634Lys |
S228 |
7 | BAA05g34760 | A05 | 35790769 | C | T | synonymous_variant | LOW | c.1947C>T|p.Leu649Leu |
S255 |
8 | BAA05g34760 | A05 | 35790985 | C | T | synonymous_variant | LOW | c.2163C>T|p.Tyr721Tyr |
S251 |
9 | BAA05g34760 | A05 | 35794125 | G | A | downstream_gene_variant | MODIFIER | c.*3128G>A| |
S178 |