Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g43230 | A01 | 28648592 | C | T | missense_variant | MODERATE | c.2080G>A|p.Ala694Thr |
S34 |
2 | BAA01g43230 | A01 | 28649019 | C | T | synonymous_variant | LOW | c.1653G>A|p.Thr551Thr |
S265 |
3 | BAA01g43230 | A01 | 28649217 | A | C | synonymous_variant | LOW | c.1455T>G|p.Val485Val |
S1 S132 S156 S176 S20 S200 S202 S203 S218 S240 S241 S263 S27 S295 S42 S49 S55 S6 S70 |
4 | BAA01g43230 | A01 | 28650017 | C | T | missense_variant | MODERATE | c.655G>A|p.Asp219Asn |
S217 |
5 | BAA01g43230 | A01 | 28652485 | C | T | upstream_gene_variant | MODIFIER | c.-1814G>A| |
S207 |
6 | BAA01g43230 | A01 | 28653684 | T | C | upstream_gene_variant | MODIFIER | c.-3013A>G| |
S33 |
7 | BAA01g43230 | A01 | 28653914 | G | A | upstream_gene_variant | MODIFIER | c.-3243C>T| |
S35 |
8 | BAA01g43230 | A01 | 28655119 | C | T | upstream_gene_variant | MODIFIER | c.-4448G>A| |
S204 |