Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g18670 | A01 | 9166290 | C | T | missense_variant | MODERATE | c.79C>T|p.Pro27Ser |
S182 |
2 | BAA01g18670 | A01 | 9167170 | G | A | synonymous_variant | LOW | c.534G>A|p.Lys178Lys |
S124 |
3 | BAA01g18670 | A01 | 9168518 | G | A | stop_gained | HIGH | c.1511G>A|p.Trp504* |
S5 |
4 | BAA01g18670 | A01 | 9169184 | C | T | splice_region_variant&intron_variant | LOW | c.2041-5C>T| |
S250 |
5 | BAA01g18670 | A01 | 9170997 | G | A | downstream_gene_variant | MODIFIER | c.*1593G>A| |
S162 |
6 | BAA01g18670 | A01 | 9171200 | G | A | downstream_gene_variant | MODIFIER | c.*1796G>A| |
S15 S3 |
7 | BAA01g18670 | A01 | 9171766 | G | A | downstream_gene_variant | MODIFIER | c.*2362G>A| |
S168 |