Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g18520 | A02 | 9435324 | G | A | synonymous_variant | LOW | c.1831C>T|p.Leu611Leu |
S293 |
2 | BAA02g18520 | A02 | 9436957 | C | T | splice_region_variant&intron_variant | LOW | c.1387+5G>A| |
S292 |
3 | BAA02g18520 | A02 | 9437226 | C | T | missense_variant | MODERATE | c.1123G>A|p.Gly375Ser |
S245 |
4 | BAA02g18520 | A02 | 9437501 | C | T | missense_variant | MODERATE | c.848G>A|p.Arg283Lys |
S46 |
5 | BAA02g18520 | A02 | 9437610 | G | A | missense_variant | MODERATE | c.739C>T|p.Leu247Phe |
S264 |
6 | BAA02g18520 | A02 | 9438592 | C | T | missense_variant | MODERATE | c.211G>A|p.Glu71Lys |
S200 |
7 | BAA02g18520 | A02 | 9438841 | C | T | upstream_gene_variant | MODIFIER | c.-39G>A| |
S301 S304 |
8 | BAA02g18520 | A02 | 9439511 | G | A | upstream_gene_variant | MODIFIER | c.-709C>T| |
S132 S137 S215 |
9 | BAA02g18520 | A02 | 9440111 | C | T | upstream_gene_variant | MODIFIER | c.-1309G>A| |
S249 |