Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g16500 | A05 | 9144739 | G | T | upstream_gene_variant | MODIFIER | c.-4692G>T| |
S168 |
2 | BAA05g16500 | A05 | 9145224 | C | T | upstream_gene_variant | MODIFIER | c.-4207C>T| |
S72 S78 |
3 | BAA05g16500 | A05 | 9145293 | G | A | upstream_gene_variant | MODIFIER | c.-4138G>A| |
S252 |
4 | BAA05g16500 | A05 | 9145914 | C | T | upstream_gene_variant | MODIFIER | c.-3517C>T| |
S188 |
5 | BAA05g16500 | A05 | 9146112 | C | T | upstream_gene_variant | MODIFIER | c.-3319C>T| |
S81 S85 |
6 | BAA05g16500 | A05 | 9148020 | G | A | upstream_gene_variant | MODIFIER | c.-1411G>A| |
S292 |
7 | BAA05g16500 | A05 | 9148208 | C | T | upstream_gene_variant | MODIFIER | c.-1223C>T| |
S281 |
8 | BAA05g16500 | A05 | 9148923 | C | T | upstream_gene_variant | MODIFIER | c.-508C>T| |
S45 |
9 | BAA05g16500 | A05 | 9150327 | A | G | missense_variant | MODERATE | c.845A>G|p.Asp282Gly |
S80 |
10 | BAA05g16500 | A05 | 9150550 | C | T | downstream_gene_variant | MODIFIER | c.*66C>T| |
S18 |
11 | BAA05g16500 | A05 | 9150853 | C | T | downstream_gene_variant | MODIFIER | c.*369C>T| |
S237 |
12 | BAA05g16500 | A05 | 9151765 | G | A | downstream_gene_variant | MODIFIER | c.*1281G>A| |
S172 S217 |
13 | BAA05g16500 | A05 | 9151907 | C | T | downstream_gene_variant | MODIFIER | c.*1423C>T| |
S255 |
14 | BAA05g16500 | A05 | 9152152 | G | A | downstream_gene_variant | MODIFIER | c.*1668G>A| |
S282 |
15 | BAA05g16500 | A05 | 9152250 | G | A | downstream_gene_variant | MODIFIER | c.*1766G>A| |
S25 |
16 | BAA05g16500 | A05 | 9152750 | C | T | downstream_gene_variant | MODIFIER | c.*2266C>T| |
S20 |
17 | BAA05g16500 | A05 | 9153173 | G | A | downstream_gene_variant | MODIFIER | c.*2689G>A| |
S107 |