Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g25220 | A05 | 30101327 | G | A | synonymous_variant | LOW | c.261G>A|p.Arg87Arg |
S238 |
2 | BAA05g25220 | A05 | 30102342 | C | T | missense_variant | MODERATE | c.1276C>T|p.His426Tyr |
S103 |
3 | BAA05g25220 | A05 | 30102477 | G | A | missense_variant | MODERATE | c.1411G>A|p.Val471Ile |
S5 |
4 | BAA05g25220 | A05 | 30102695 | C | T | synonymous_variant | LOW | c.1629C>T|p.Phe543Phe |
S269 |
5 | BAA05g25220 | A05 | 30103013 | G | A | synonymous_variant | LOW | c.1881G>A|p.Gln627Gln |
S291 |
6 | BAA05g25220 | A05 | 30105111 | G | A | downstream_gene_variant | MODIFIER | c.*1519G>A| |
S188 |
7 | BAA05g25220 | A05 | 30107599 | G | A | downstream_gene_variant | MODIFIER | c.*4007G>A| |
S9 |
8 | BAA05g25220 | A05 | 30107811 | C | T | downstream_gene_variant | MODIFIER | c.*4219C>T| |
S233 |
9 | BAA05g25220 | A05 | 30108563 | C | T | downstream_gene_variant | MODIFIER | c.*4971C>T| |
S294 |