Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g16500 | A01 | 8016321 | C | T | missense_variant | MODERATE | c.2020G>A|p.Ala674Thr |
S306 S308 |
2 | BAA01g16500 | A01 | 8017173 | G | A | missense_variant | MODERATE | c.1610C>T|p.Ser537Phe |
S249 |
3 | BAA01g16500 | A01 | 8017259 | C | T | splice_region_variant&intron_variant | LOW | c.1528-4G>A| |
S185 |
4 | BAA01g16500 | A01 | 8017887 | G | A | missense_variant | MODERATE | c.1184C>T|p.Ser395Phe |
S139 |
5 | BAA01g16500 | A01 | 8020702 | C | T | missense_variant | MODERATE | c.224G>A|p.Ser75Asn |
S20 |
6 | BAA01g16500 | A01 | 8021173 | G | A | stop_gained | HIGH | c.100C>T|p.Gln34* |
S293 |
7 | BAA01g16500 | A01 | 8021565 | G | A | upstream_gene_variant | MODIFIER | c.-293C>T| |
S8 |
8 | BAA01g16500 | A01 | 8021794 | G | A | upstream_gene_variant | MODIFIER | c.-522C>T| |
S142 |
9 | BAA01g16500 | A01 | 8022501 | C | T | upstream_gene_variant | MODIFIER | c.-1229G>A| |
S275 |
10 | BAA01g16500 | A01 | 8023240 | G | A | upstream_gene_variant | MODIFIER | c.-1968C>T| |
S124 |
11 | BAA01g16500 | A01 | 8023261 | G | A | upstream_gene_variant | MODIFIER | c.-1989C>T| |
S56 |
12 | BAA01g16500 | A01 | 8025572 | G | A | upstream_gene_variant | MODIFIER | c.-4300C>T| |
S276 |