Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g26860 | A01 | 15144027 | C | T | downstream_gene_variant | MODIFIER | c.*3276G>A| |
S139 |
2 | BAA01g26860 | A01 | 15148028 | C | T | missense_variant | MODERATE | c.1444G>A|p.Ala482Thr |
S25 S259 |
3 | BAA01g26860 | A01 | 15148112 | C | T | missense_variant | MODERATE | c.1360G>A|p.Glu454Lys |
S189 |
4 | BAA01g26860 | A01 | 15148242 | C | T | synonymous_variant | LOW | c.1230G>A|p.Lys410Lys |
S55 |
5 | BAA01g26860 | A01 | 15148340 | C | T | missense_variant | MODERATE | c.1132G>A|p.Asp378Asn |
S20 |
6 | BAA01g26860 | A01 | 15149701 | C | T | upstream_gene_variant | MODIFIER | c.-230G>A| |
S20 |
7 | BAA01g26860 | A01 | 15152843 | G | A | upstream_gene_variant | MODIFIER | c.-3372C>T| |
S246 |
8 | BAA01g26860 | A01 | 15153352 | G | A | upstream_gene_variant | MODIFIER | c.-3881C>T| |
S202 |
9 | BAA01g26860 | A01 | 15153588 | C | T | upstream_gene_variant | MODIFIER | c.-4117G>A| |
S275 |