Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g05140 | A01 | 2256654 | G | A | upstream_gene_variant | MODIFIER | c.-4989G>A| |
S280 |
2 | BAA01g05140 | A01 | 2258267 | G | A | upstream_gene_variant | MODIFIER | c.-3376G>A| |
S83 S88 |
3 | BAA01g05140 | A01 | 2261810 | G | A | synonymous_variant | LOW | c.168G>A|p.Glu56Glu |
S180 |
4 | BAA01g05140 | A01 | 2263592 | G | A | synonymous_variant | LOW | c.1182G>A|p.Gln394Gln |
S183 S198 |
5 | BAA01g05140 | A01 | 2264146 | G | A | splice_acceptor_variant&intron_variant | HIGH | c.1428-1G>A| |
S186 |
6 | BAA01g05140 | A01 | 2265310 | C | T | missense_variant | MODERATE | c.2131C>T|p.Pro711Ser |
S99 |
7 | BAA01g05140 | A01 | 2265736 | C | T | stop_gained | HIGH | c.2476C>T|p.Gln826* |
S151 |
8 | BAA01g05140 | A01 | 2266067 | G | A | missense_variant | MODERATE | c.2696G>A|p.Ser899Asn |
S146 |
9 | BAA01g05140 | A01 | 2267555 | G | A | downstream_gene_variant | MODIFIER | c.*1095G>A| |
S156 |
10 | BAA01g05140 | A01 | 2268326 | G | A | downstream_gene_variant | MODIFIER | c.*1866G>A| |
S86 |
11 | BAA01g05140 | A01 | 2270043 | G | A | downstream_gene_variant | MODIFIER | c.*3583G>A| |
S123 |