Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g26560 | A05 | 31188845 | G | A | upstream_gene_variant | MODIFIER | c.-4791G>A| |
S203 |
2 | BAA05g26560 | A05 | 31189085 | C | T | upstream_gene_variant | MODIFIER | c.-4551C>T| |
S295 |
3 | BAA05g26560 | A05 | 31189281 | C | T | upstream_gene_variant | MODIFIER | c.-4355C>T| |
S245 |
4 | BAA05g26560 | A05 | 31189343 | G | A | upstream_gene_variant | MODIFIER | c.-4293G>A| |
S9 |
5 | BAA05g26560 | A05 | 31189425 | C | T | upstream_gene_variant | MODIFIER | c.-4211C>T| |
S165 |
6 | BAA05g26560 | A05 | 31190350 | C | T | upstream_gene_variant | MODIFIER | c.-3286C>T| |
S146 |
7 | BAA05g26560 | A05 | 31193041 | G | A | upstream_gene_variant | MODIFIER | c.-595G>A| |
S188 |
8 | BAA05g26560 | A05 | 31193098 | C | T | upstream_gene_variant | MODIFIER | c.-538C>T| |
S204 |
9 | BAA05g26560 | A05 | 31194311 | C | T | missense_variant | MODERATE | c.676C>T|p.Arg226Trp |
S235 S292 |
10 | BAA05g26560 | A05 | 31194487 | G | A | synonymous_variant | LOW | c.852G>A|p.Lys284Lys |
S238 |
11 | BAA05g26560 | A05 | 31194550 | C | T | synonymous_variant | LOW | c.915C>T|p.Leu305Leu |
S261 |
12 | BAA05g26560 | A05 | 31197483 | C | T | downstream_gene_variant | MODIFIER | c.*2636C>T| |
S180 |
13 | BAA05g26560 | A05 | 31198010 | G | A | downstream_gene_variant | MODIFIER | c.*3163G>A| |
S296 |
14 | BAA05g26560 | A05 | 31198076 | C | T | downstream_gene_variant | MODIFIER | c.*3229C>T| |
S69 |
15 | BAA05g26560 | A05 | 31199583 | C | T | downstream_gene_variant | MODIFIER | c.*4736C>T| |
S277 |