Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05000 | A01 | 2204337 | G | A | upstream_gene_variant | MODIFIER | c.-4632G>A| |
S202 |
2 | BAA01g05000 | A01 | 2205096 | G | A | upstream_gene_variant | MODIFIER | c.-3873G>A| |
S73 S91 |
3 | BAA01g05000 | A01 | 2209937 | C | T | synonymous_variant | LOW | c.558C>T|p.Ser186Ser |
S260 |
4 | BAA01g05000 | A01 | 2210049 | C | T | missense_variant | MODERATE | c.593C>T|p.Thr198Ile |
S205 |
5 | BAA01g05000 | A01 | 2210677 | G | A | missense_variant | MODERATE | c.842G>A|p.Arg281His |
S172 S217 |
6 | BAA01g05000 | A01 | 2211113 | G | A | missense_variant | MODERATE | c.1207G>A|p.Ala403Thr |
S72 S78 |
7 | BAA01g05000 | A01 | 2211378 | G | A | missense_variant | MODERATE | c.1472G>A|p.Arg491Lys |
S156 |
8 | BAA01g05000 | A01 | 2211531 | G | T | stop_gained | HIGH | c.1546G>T|p.Glu516* |
S250 |
9 | BAA01g05000 | A01 | 2211622 | G | A | missense_variant | MODERATE | c.1637G>A|p.Cys546Tyr |
S204 |
10 | BAA01g05000 | A01 | 2211823 | C | T | missense_variant | MODERATE | c.1838C>T|p.Ser613Leu |
S107 |
11 | BAA01g05000 | A01 | 2212049 | G | A | downstream_gene_variant | MODIFIER | c.*213G>A| |
S199 |
12 | BAA01g05000 | A01 | 2213808 | G | A | downstream_gene_variant | MODIFIER | c.*1972G>A| |
S177 |
13 | BAA01g05000 | A01 | 2214063 | G | A | downstream_gene_variant | MODIFIER | c.*2227G>A| |
S303 |