Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA01g17960 | A01 | 8788178 | T | C | upstream_gene_variant | MODIFIER | c.-4166T>C| |
S161 |
2 | BAA01g17960 | A01 | 8788992 | C | T | upstream_gene_variant | MODIFIER | c.-3352C>T| |
S277 |
3 | BAA01g17960 | A01 | 8789149 | G | A | upstream_gene_variant | MODIFIER | c.-3195G>A| |
S72 S78 |
4 | BAA01g17960 | A01 | 8790509 | G | A | upstream_gene_variant | MODIFIER | c.-1835G>A| |
S96 |
5 | BAA01g17960 | A01 | 8791486 | G | A | upstream_gene_variant | MODIFIER | c.-858G>A| |
S204 |
6 | BAA01g17960 | A01 | 8791581 | C | T | upstream_gene_variant | MODIFIER | c.-763C>T| |
S125 |
7 | BAA01g17960 | A01 | 8792419 | C | T | missense_variant | MODERATE | c.76C>T|p.Pro26Ser |
S17 |
8 | BAA01g17960 | A01 | 8794196 | G | A | missense_variant | MODERATE | c.517G>A|p.Gly173Arg |
S263 |
9 | BAA01g17960 | A01 | 8795212 | C | T | missense_variant | MODERATE | c.1093C>T|p.Arg365Cys |
S67 |
10 | BAA01g17960 | A01 | 8795253 | C | T | synonymous_variant | LOW | c.1134C>T|p.Leu378Leu |
S62 |
11 | BAA01g17960 | A01 | 8795450 | G | C | downstream_gene_variant | MODIFIER | c.*134G>C| |
S143 |
12 | BAA01g17960 | A01 | 8796464 | G | A | downstream_gene_variant | MODIFIER | c.*1148G>A| |
S59 |