Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g03690 | A01 | 1680747 | G | A | synonymous_variant | LOW | c.522G>A|p.Ser174Ser |
S247 |
2 | BAA01g03690 | A01 | 1680850 | G | A | missense_variant | MODERATE | c.625G>A|p.Glu209Lys |
S190 |
3 | BAA01g03690 | A01 | 1681073 | C | T | missense_variant | MODERATE | c.848C>T|p.Ala283Val |
S218 |
4 | BAA01g03690 | A01 | 1681340 | C | T | missense_variant | MODERATE | c.1115C>T|p.Thr372Met |
S189 |
5 | BAA01g03690 | A01 | 1682220 | C | T | synonymous_variant | LOW | c.1419C>T|p.Phe473Phe |
S137 |
6 | BAA01g03690 | A01 | 1682264 | C | T | missense_variant | MODERATE | c.1463C>T|p.Pro488Leu |
S100 |
7 | BAA01g03690 | A01 | 1682267 | C | T | missense_variant | MODERATE | c.1466C>T|p.Thr489Ile |
S208 S219 |
8 | BAA01g03690 | A01 | 1682408 | G | A | missense_variant | MODERATE | c.1607G>A|p.Gly536Glu |
S159 S188 S243 S276 S298 S299 |
9 | BAA01g03690 | A01 | 1683127 | G | A | downstream_gene_variant | MODIFIER | c.*679G>A| |
S157 S163 |
10 | BAA01g03690 | A01 | 1683228 | G | A | downstream_gene_variant | MODIFIER | c.*780G>A| |
S263 |