Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g10190 | A01 | 4622970 | C | T | downstream_gene_variant | MODIFIER | c.*3357G>A| |
S100 |
2 | BAA01g10190 | A01 | 4623122 | C | T | downstream_gene_variant | MODIFIER | c.*3205G>A| |
S244 |
3 | BAA01g10190 | A01 | 4626353 | G | A | missense_variant | MODERATE | c.892C>T|p.Pro298Ser |
S10 |
4 | BAA01g10190 | A01 | 4626394 | G | A | missense_variant | MODERATE | c.851C>T|p.Ser284Phe |
S292 |
5 | BAA01g10190 | A01 | 4626778 | G | A | missense_variant | MODERATE | c.467C>T|p.Thr156Ile |
S92 |
6 | BAA01g10190 | A01 | 4626882 | G | A | synonymous_variant | LOW | c.363C>T|p.Leu121Leu |
S193 |
7 | BAA01g10190 | A01 | 4627199 | G | A | missense_variant | MODERATE | c.248C>T|p.Thr83Ile |
S239 |
8 | BAA01g10190 | A01 | 4627509 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.7-1G>A| |
S89 |
9 | BAA01g10190 | A01 | 4627990 | G | A | upstream_gene_variant | MODIFIER | c.-114C>T| |
S139 |
10 | BAA01g10190 | A01 | 4628521 | G | A | upstream_gene_variant | MODIFIER | c.-645C>T| |
S194 |
11 | BAA01g10190 | A01 | 4630724 | C | T | upstream_gene_variant | MODIFIER | c.-2848G>A| |
S135 |