Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g30070 | A01 | 19084758 | G | A | missense_variant | MODERATE | c.2590C>T|p.Leu864Phe |
S208 S219 |
2 | BAA01g30070 | A01 | 19085213 | C | T | missense_variant | MODERATE | c.2239G>A|p.Gly747Arg |
S211 S227 |
3 | BAA01g30070 | A01 | 19085446 | A | T | missense_variant | MODERATE | c.2006T>A|p.Ile669Lys |
S217 S248 |
4 | BAA01g30070 | A01 | 19088592 | G | A | missense_variant | MODERATE | c.206C>T|p.Pro69Leu |
S105 S106 |
5 | BAA01g30070 | A01 | 19088713 | G | A | missense_variant | MODERATE | c.85C>T|p.Pro29Ser |
S155 S211 |
6 | BAA01g30070 | A01 | 19088729 | C | T | synonymous_variant | LOW | c.69G>A|p.Pro23Pro |
S208 S93 |
7 | BAA01g30070 | A01 | 19088767 | C | T | missense_variant | MODERATE | c.31G>A|p.Ala11Thr |
S128 |
8 | BAA01g30070 | A01 | 19089087 | C | T | upstream_gene_variant | MODIFIER | c.-290G>A| |
S275 |
9 | BAA01g30070 | A01 | 19089214 | C | T | upstream_gene_variant | MODIFIER | c.-417G>A| |
S185 |
10 | BAA01g30070 | A01 | 19090623 | A | G | upstream_gene_variant | MODIFIER | c.-1826T>C| |
S171 |