Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g12400 | A01 | 5842109 | C | T | missense_variant | MODERATE | c.2087G>A|p.Gly696Glu |
S1 S90 |
2 | BAA01g12400 | A01 | 5842221 | G | A | missense_variant | MODERATE | c.1975C>T|p.Pro659Ser |
S156 |
3 | BAA01g12400 | A01 | 5842240 | C | T | synonymous_variant | LOW | c.1956G>A|p.Glu652Glu |
S152 |
4 | BAA01g12400 | A01 | 5842475 | G | A | synonymous_variant | LOW | c.1780C>T|p.Leu594Leu |
S149 |
5 | BAA01g12400 | A01 | 5842506 | C | T | synonymous_variant | LOW | c.1749G>A|p.Lys583Lys |
S25 S264 |
6 | BAA01g12400 | A01 | 5842778 | C | T | missense_variant | MODERATE | c.1477G>A|p.Glu493Lys |
S38 |
7 | BAA01g12400 | A01 | 5842781 | C | T | missense_variant | MODERATE | c.1474G>A|p.Glu492Lys |
S211 S227 |
8 | BAA01g12400 | A01 | 5843798 | C | T | missense_variant | MODERATE | c.457G>A|p.Gly153Arg |
S150 |
9 | BAA01g12400 | A01 | 5848780 | G | A | upstream_gene_variant | MODIFIER | c.-4526C>T| |
S123 |
10 | BAA01g12400 | A01 | 5849013 | G | A | upstream_gene_variant | MODIFIER | c.-4759C>T| |
S156 |