Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17250 | A01 | 8361659 | G | A | missense_variant | MODERATE | c.2375C>T|p.Ala792Val |
S32 |
2 | BAA01g17250 | A01 | 8363497 | C | T | splice_region_variant&intron_variant | LOW | c.540-3G>A| |
S261 |
3 | BAA01g17250 | A01 | 8364748 | C | T | missense_variant | MODERATE | c.104G>A|p.Gly35Glu |
S81 S85 |
4 | BAA01g17250 | A01 | 8366385 | C | T | upstream_gene_variant | MODIFIER | c.-1534G>A| |
S71 |
5 | BAA01g17250 | A01 | 8366760 | C | T | upstream_gene_variant | MODIFIER | c.-1909G>A| |
S221 |
6 | BAA01g17250 | A01 | 8366940 | C | A | upstream_gene_variant | MODIFIER | c.-2089G>T| |
S269 |