Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g02350 | A03 | 1051678 | G | A | synonymous_variant | LOW | c.1695C>T|p.Asp565Asp |
S208 S93 |
2 | BAA03g02350 | A03 | 1051896 | G | A | synonymous_variant | LOW | c.1477C>T|p.Leu493Leu |
S270 |
3 | BAA03g02350 | A03 | 1052887 | C | T | missense_variant | MODERATE | c.724G>A|p.Ala242Thr |
S80 |
4 | BAA03g02350 | A03 | 1053087 | C | T | missense_variant | MODERATE | c.613G>A|p.Glu205Lys |
S19 |
5 | BAA03g02350 | A03 | 1053400 | G | A | synonymous_variant | LOW | c.498C>T|p.Ile166Ile |
S255 |
6 | BAA03g02350 | A03 | 1053687 | G | A | missense_variant | MODERATE | c.274C>T|p.Pro92Ser |
S297 |
7 | BAA03g02350 | A03 | 1054186 | G | A | missense_variant | MODERATE | c.68C>T|p.Ala23Val |
S282 |
8 | BAA03g02350 | A03 | 1055272 | G | A | upstream_gene_variant | MODIFIER | c.-1019C>T| |
S279 |
9 | BAA03g02350 | A03 | 1058295 | G | A | upstream_gene_variant | MODIFIER | c.-4042C>T| |
S217 S248 |