Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g35000 | A02 | 30100677 | G | A | synonymous_variant | LOW | c.75G>A|p.Lys25Lys |
S209 |
2 | BAA02g35000 | A02 | 30101698 | C | T | missense_variant | MODERATE | c.1015C>T|p.His339Tyr |
S138 |
3 | BAA02g35000 | A02 | 30101984 | G | A | missense_variant | MODERATE | c.1301G>A|p.Arg434Lys |
S246 |
4 | BAA02g35000 | A02 | 30102244 | G | A | missense_variant | MODERATE | c.1561G>A|p.Asp521Asn |
S110 |
5 | BAA02g35000 | A02 | 30102511 | G | A | missense_variant | MODERATE | c.1742G>A|p.Arg581Lys |
S95 |
6 | BAA02g35000 | A02 | 30105784 | C | T | downstream_gene_variant | MODIFIER | c.*956C>T| |
S202 |
7 | BAA02g35000 | A02 | 30106989 | G | A | downstream_gene_variant | MODIFIER | c.*2161G>A| |
S229 |
8 | BAA02g35000 | A02 | 30107504 | C | T | downstream_gene_variant | MODIFIER | c.*2676C>T| |
S42 |
9 | BAA02g35000 | A02 | 30107762 | G | A | downstream_gene_variant | MODIFIER | c.*2934G>A| |
S5 |
10 | BAA02g35000 | A02 | 30107799 | G | A | downstream_gene_variant | MODIFIER | c.*2971G>A| |
S80 |