Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g14550 | A01 | 6902518 | G | A | missense_variant | MODERATE | c.1256C>T|p.Ser419Phe |
S9 |
2 | BAA01g14550 | A01 | 6903026 | C | T | splice_region_variant&intron_variant | LOW | c.1041+5G>A| |
S259 |
3 | BAA01g14550 | A01 | 6905822 | G | A | upstream_gene_variant | MODIFIER | c.-1310C>T| |
S105 S106 |
4 | BAA01g14550 | A01 | 6905990 | C | T | upstream_gene_variant | MODIFIER | c.-1478G>A| |
S299 |
5 | BAA01g14550 | A01 | 6907019 | C | T | upstream_gene_variant | MODIFIER | c.-2507G>A| |
S159 S188 S243 S276 S298 S299 |
6 | BAA01g14550 | A01 | 6908736 | G | A | upstream_gene_variant | MODIFIER | c.-4224C>T| |
S28 |
7 | BAA01g14550 | A01 | 6908953 | G | A | upstream_gene_variant | MODIFIER | c.-4441C>T| |
S12 |