Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA03g44280 | A03 | 21013406 | C | T | upstream_gene_variant | MODIFIER | c.-1927C>T| |
S250 |
2 | BAA03g44280 | A03 | 21014059 | G | A | upstream_gene_variant | MODIFIER | c.-1274G>A| |
S103 |
3 | BAA03g44280 | A03 | 21015712 | A | G | missense_variant&splice_region_variant | MODERATE | c.235A>G|p.Lys79Glu |
S299 |
4 | BAA03g44280 | A03 | 21017986 | G | A | missense_variant | MODERATE | c.1048G>A|p.Gly350Arg |
S210 |
5 | BAA03g44280 | A03 | 21017987 | G | A | missense_variant | MODERATE | c.1049G>A|p.Gly350Glu |
S188 |
6 | BAA03g44280 | A03 | 21019469 | C | T | synonymous_variant | LOW | c.1692C>T|p.Leu564Leu |
S265 S273 |
7 | BAA03g44280 | A03 | 21020451 | C | T | downstream_gene_variant | MODIFIER | c.*404C>T| |
S87 |
8 | BAA03g44280 | A03 | 21020457 | G | A | downstream_gene_variant | MODIFIER | c.*410G>A| |
S28 |
9 | BAA03g44280 | A03 | 21021000 | C | T | downstream_gene_variant | MODIFIER | c.*953C>T| |
S19 |