Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g04930 | A02 | 2151710 | C | T | upstream_gene_variant | MODIFIER | c.-3572C>T| |
S200 |
2 | BAA02g04930 | A02 | 2155459 | C | T | missense_variant | MODERATE | c.67C>T|p.Pro23Ser |
S75 S81 |
3 | BAA02g04930 | A02 | 2155500 | G | A | synonymous_variant | LOW | c.108G>A|p.Lys36Lys |
S67 |
4 | BAA02g04930 | A02 | 2157451 | G | A | synonymous_variant | LOW | c.1002G>A|p.Thr334Thr |
S223 |
5 | BAA02g04930 | A02 | 2160343 | C | T | missense_variant | MODERATE | c.2818C>T|p.Pro940Ser |
S58 |
6 | BAA02g04930 | A02 | 2160562 | G | A | missense_variant | MODERATE | c.3037G>A|p.Glu1013Lys |
S168 |
7 | BAA02g04930 | A02 | 2160590 | G | A | missense_variant | MODERATE | c.3065G>A|p.Arg1022Lys |
S210 S225 |
8 | BAA02g04930 | A02 | 2161786 | G | A | downstream_gene_variant | MODIFIER | c.*514G>A| |
S215 |
9 | BAA02g04930 | A02 | 2161956 | G | A | downstream_gene_variant | MODIFIER | c.*684G>A| |
S302 |
10 | BAA02g04930 | A02 | 2161983 | C | T | downstream_gene_variant | MODIFIER | c.*711C>T| |
S115 |
11 | BAA02g04930 | A02 | 2162038 | C | T | downstream_gene_variant | MODIFIER | c.*766C>T| |
S18 |
12 | BAA02g04930 | A02 | 2162219 | C | T | downstream_gene_variant | MODIFIER | c.*947C>T| |
S79 S84 |