Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g21180 | A01 | 10459799 | C | T | upstream_gene_variant | MODIFIER | c.-4263C>T| |
S261 |
2 | BAA01g21180 | A01 | 10460542 | C | T | upstream_gene_variant | MODIFIER | c.-3520C>T| |
S100 |
3 | BAA01g21180 | A01 | 10464108 | C | T | missense_variant | MODERATE | c.47C>T|p.Pro16Leu |
S207 |
4 | BAA01g21180 | A01 | 10464113 | C | T | missense_variant | MODERATE | c.52C>T|p.Pro18Ser |
S36 |
5 | BAA01g21180 | A01 | 10464157 | G | A | synonymous_variant | LOW | c.96G>A|p.Lys32Lys |
S241 |
6 | BAA01g21180 | A01 | 10464270 | C | T | missense_variant | MODERATE | c.209C>T|p.Ser70Phe |
S286 |
7 | BAA01g21180 | A01 | 10464460 | G | A | synonymous_variant | LOW | c.399G>A|p.Thr133Thr |
S142 |
8 | BAA01g21180 | A01 | 10466250 | G | A | downstream_gene_variant | MODIFIER | c.*1643G>A| |
S229 |
9 | BAA01g21180 | A01 | 10466910 | C | T | downstream_gene_variant | MODIFIER | c.*2303C>T| |
S100 |