Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g41460 | A01 | 27555392 | G | A | missense_variant | MODERATE | c.1625C>T|p.Ala542Val |
S71 |
2 | BAA01g41460 | A01 | 27556065 | G | A | missense_variant | MODERATE | c.1325C>T|p.Ala442Val |
S104 |
3 | BAA01g41460 | A01 | 27556230 | C | T | splice_region_variant&intron_variant | LOW | c.1248+3G>A| |
S210 S225 |
4 | BAA01g41460 | A01 | 27556756 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.913-1G>A| |
S183 |
5 | BAA01g41460 | A01 | 27558455 | C | T | missense_variant | MODERATE | c.223G>A|p.Val75Ile |
S251 |
6 | BAA01g41460 | A01 | 27559064 | C | T | upstream_gene_variant | MODIFIER | c.-307G>A| |
S269 |
7 | BAA01g41460 | A01 | 27559303 | G | A | upstream_gene_variant | MODIFIER | c.-546C>T| |
S306 |
8 | BAA01g41460 | A01 | 27559467 | G | A | upstream_gene_variant | MODIFIER | c.-710C>T| |
S123 |
9 | BAA01g41460 | A01 | 27561866 | C | T | upstream_gene_variant | MODIFIER | c.-3109G>A| |
S118 |
10 | BAA01g41460 | A01 | 27562771 | G | A | upstream_gene_variant | MODIFIER | c.-4014C>T| |
S190 |