Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA02g32660 | A02 | 27766604 | G | A | downstream_gene_variant | MODIFIER | c.*4833C>T| |
S225 |
2 | BAA02g32660 | A02 | 27767375 | G | A | downstream_gene_variant | MODIFIER | c.*4062C>T| |
S126 |
3 | BAA02g32660 | A02 | 27768736 | G | A | downstream_gene_variant | MODIFIER | c.*2701C>T| |
S191 |
4 | BAA02g32660 | A02 | 27769572 | C | T | downstream_gene_variant | MODIFIER | c.*1865G>A| |
S142 |
5 | BAA02g32660 | A02 | 27771237 | C | T | downstream_gene_variant | MODIFIER | c.*200G>A| |
S239 |
6 | BAA02g32660 | A02 | 27771702 | C | T | stop_gained | HIGH | c.1239G>A|p.Trp413* |
S180 |
7 | BAA02g32660 | A02 | 27772664 | C | T | missense_variant | MODERATE | c.640G>A|p.Asp214Asn |
S6 |
8 | BAA02g32660 | A02 | 27774254 | C | T | intron_variant | MODIFIER | c.118+353G>A| |
S139 |
9 | BAA02g32660 | A02 | 27774386 | C | T | intron_variant | MODIFIER | c.118+221G>A| |
S131 |
10 | BAA02g32660 | A02 | 27774424 | C | T | intron_variant | MODIFIER | c.118+183G>A| |
S183 S198 |
11 | BAA02g32660 | A02 | 27774655 | C | T | missense_variant | MODERATE | c.70G>A|p.Asp24Asn |
S172 |
12 | BAA02g32660 | A02 | 27776098 | T | C | upstream_gene_variant | MODIFIER | c.-1374A>G| |
S234 |
13 | BAA02g32660 | A02 | 27776296 | C | T | upstream_gene_variant | MODIFIER | c.-1572G>A| |
S168 |