Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g27770 | A02 | 15611430 | C | T | synonymous_variant | LOW | c.10C>T|p.Leu4Leu |
S119 |
2 | BAA02g27770 | A02 | 15611524 | C | T | missense_variant | MODERATE | c.104C>T|p.Ala35Val |
S2 |
3 | BAA02g27770 | A02 | 15611661 | G | A | missense_variant | MODERATE | c.241G>A|p.Asp81Asn |
S247 |
4 | BAA02g27770 | A02 | 15612082 | G | A | missense_variant | MODERATE | c.488G>A|p.Arg163Lys |
S37 |
5 | BAA02g27770 | A02 | 15612367 | C | T | missense_variant | MODERATE | c.773C>T|p.Ser258Phe |
S162 |
6 | BAA02g27770 | A02 | 15613397 | C | T | missense_variant | MODERATE | c.1190C>T|p.Ala397Val |
S299 |
7 | BAA02g27770 | A02 | 15615858 | C | T | downstream_gene_variant | MODIFIER | c.*2304C>T| |
S31 |
8 | BAA02g27770 | A02 | 15616177 | A | T | downstream_gene_variant | MODIFIER | c.*2623A>T| |
S18 |
9 | BAA02g27770 | A02 | 15616911 | G | A | downstream_gene_variant | MODIFIER | c.*3357G>A| |
S55 |